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Entry version 197 (16 Oct 2019)
Sequence version 3 (30 May 2000)
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Protein

Retinal-specific phospholipid-transporting ATPase ABCA4

Gene

ABCA4

Organism
Homo sapiens (Human)
Status
Reviewed-Annotation score:

Annotation score:5 out of 5

<p>The annotation score provides a heuristic measure of the annotation content of a UniProtKB entry or proteome. This score <strong>cannot</strong> be used as a measure of the accuracy of the annotation as we cannot define the ‘correct annotation’ for any given protein.<p><a href='/help/annotation_score' target='_top'>More...</a></p>
-Experimental evidence at protein leveli <p>This indicates the type of evidence that supports the existence of the protein. Note that the ‘protein existence’ evidence does not give information on the accuracy or correctness of the sequence(s) displayed.<p><a href='/help/protein_existence' target='_top'>More...</a></p>

<p>This section provides any useful information about the protein, mostly biological knowledge.<p><a href='/help/function_section' target='_top'>More...</a></p>Functioni

Catalyzes the translocation of specific phospholipids from the extracellular/lumenal to the cytoplasmic leaflet of membrane coupled to the hydrolysis of ATP (PubMed:24097981). Transports preferentially phosphatidylethanolamine (PubMed:24097981). In the visual cycle, acts as an inward-directed retinoid flipase, retinoid substrates imported by ABCA4 from the extracellular or intradiscal (rod) membrane surfaces to the cytoplasmic membrane surface are all-trans-retinaldehyde (ATR) and N-retinyl-phosphatidyl-ethanolamine (NR-PE). Once transported to the cytoplasmic surface, ATR is reduced to vitamin A by trans-retinol dehydrogenase (tRDH) and then transferred to the retinal pigment epithelium (RPE) where it is converted to 11-cis-retinal. May play a role in photoresponse, removing ATR/NR-PE from the extracellular photoreceptor surfaces during bleach recovery.2 Publications

<p>This subsection of the <a href="http://www.uniprot.org/help/function_section">Function</a> section describes the catalytic activity of an enzyme, i.e. a chemical reaction that the enzyme catalyzes.<p><a href='/help/catalytic_activity' target='_top'>More...</a></p>Catalytic activityi

  • ATP + H(2)O + phospholipid(Side 1) = ADP + phosphate + phospholipid(Side 2).1 Publication EC:7.6.2.1

<p>This subsection of the <a href="http://www.uniprot.org/help/function_section">Function</a> section describes regulatory mechanisms for enzymes, transporters or microbial transcription factors, and reports the components which regulate (by activation or inhibition) the reaction.<p><a href='/help/activity_regulation' target='_top'>More...</a></p>Activity regulationi

ATPase activity is decreased by cholesterol and ceramide. ATPase activity is stimulated by phosphatidylethanolamine. Phospholipids translocase activity is highly reduced by berylium fluoride and aluminum floride. N-ethylmaleimide inhibits phospholipid translocase activity.1 Publication

Regions

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the <a href="http://www.uniprot.org/help/function_section">Function</a> section describes a region in the protein which binds nucleotide phosphates. It always involves more than one amino acid and includes all residues involved in nucleotide-binding.<p><a href='/help/np_bind' target='_top'>More...</a></p>Nucleotide bindingi963 – 970ATP 1PROSITE-ProRule annotation8
Nucleotide bindingi1972 – 1979ATP 2PROSITE-ProRule annotation8

<p>The <a href="http://www.geneontology.org/">Gene Ontology (GO)</a> project provides a set of hierarchical controlled vocabulary split into 3 categories:<p><a href='/help/gene_ontology' target='_top'>More...</a></p>GO - Molecular functioni

GO - Biological processi

<p>UniProtKB Keywords constitute a <a href="http://www.uniprot.org/keywords">controlled vocabulary</a> with a hierarchical structure. Keywords summarise the content of a UniProtKB entry and facilitate the search for proteins of interest.<p><a href='/help/keywords' target='_top'>More...</a></p>Keywordsi

Molecular functionTranslocase
Biological processSensory transduction, Transport, Vision
LigandATP-binding, Nucleotide-binding

Enzyme and pathway databases

Reactome - a knowledgebase of biological pathways and processes

More...
Reactomei
R-HSA-2453864 Retinoid cycle disease events
R-HSA-2453902 The canonical retinoid cycle in rods (twilight vision)
R-HSA-382556 ABC-family proteins mediated transport

Protein family/group databases

Transport Classification Database

More...
TCDBi
3.A.1.211.2 the atp-binding cassette (abc) superfamily

Chemistry databases

SwissLipids knowledge resource for lipid biology

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SwissLipidsi
SLP:000000347

<p>This section provides information about the protein and gene name(s) and synonym(s) and about the organism that is the source of the protein sequence.<p><a href='/help/names_and_taxonomy_section' target='_top'>More...</a></p>Names & Taxonomyi

<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section provides an exhaustive list of all names of the protein, from commonly used to obsolete, to allow unambiguous identification of a protein.<p><a href='/help/protein_names' target='_top'>More...</a></p>Protein namesi
Recommended name:
Retinal-specific phospholipid-transporting ATPase ABCA4Curated (EC:7.6.2.11 Publication)
Alternative name(s):
ATP-binding cassette sub-family A member 4
RIM ABC transporter
Short name:
RIM protein
Short name:
RmP
Retinal-specific ATP-binding cassette transporter
Stargardt disease protein
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section indicates the name(s) of the gene(s) that code for the protein sequence(s) described in the entry. Four distinct tokens exist: ‘Name’, ‘Synonyms’, ‘Ordered locus names’ and ‘ORF names’.<p><a href='/help/gene_name' target='_top'>More...</a></p>Gene namesi
Name:ABCA4Imported
Synonyms:ABCR
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section provides information on the name(s) of the organism that is the source of the protein sequence.<p><a href='/help/organism-name' target='_top'>More...</a></p>OrganismiHomo sapiens (Human)
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section shows the unique identifier assigned by the NCBI to the source organism of the protein. This is known as the ‘taxonomic identifier’ or ‘taxid’.<p><a href='/help/taxonomic_identifier' target='_top'>More...</a></p>Taxonomic identifieri9606 [NCBI]
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section contains the taxonomic hierarchical classification lineage of the source organism. It lists the nodes as they appear top-down in the taxonomic tree, with the more general grouping listed first.<p><a href='/help/taxonomic_lineage' target='_top'>More...</a></p>Taxonomic lineageiEukaryotaMetazoaChordataCraniataVertebrataEuteleostomiMammaliaEutheriaEuarchontogliresPrimatesHaplorrhiniCatarrhiniHominidaeHomo
<p>This subsection of the <a href="http://www.uniprot.org/help/names_and_taxonomy_section">Names and taxonomy</a> section is present for entries that are part of a <a href="http://www.uniprot.org/proteomes">proteome</a>, i.e. of a set of proteins thought to be expressed by organisms whose genomes have been completely sequenced.<p><a href='/help/proteomes_manual' target='_top'>More...</a></p>Proteomesi
  • UP000005640 <p>A UniProt <a href="http://www.uniprot.org/manual/proteomes_manual">proteome</a> can consist of several components. <br></br>The component name refers to the genomic component encoding a set of proteins.<p><a href='/help/proteome_component' target='_top'>More...</a></p> Componenti: Chromosome 1

Organism-specific databases

Human Gene Nomenclature Database

More...
HGNCi
HGNC:34 ABCA4

Online Mendelian Inheritance in Man (OMIM)

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MIMi
601691 gene

neXtProt; the human protein knowledge platform

More...
neXtProti
NX_P78363

<p>This section provides information on the location and the topology of the mature protein in the cell.<p><a href='/help/subcellular_location_section' target='_top'>More...</a></p>Subcellular locationi

Extracellular region or secreted Cytosol Plasma membrane Cytoskeleton Lysosome Endosome Peroxisome ER Golgi apparatus Nucleus Mitochondrion Manual annotation Automatic computational assertionGraphics by Christian Stolte & Seán O’Donoghue; Source: COMPARTMENTS

Topology

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the <a href="http://www.uniprot.org/help/subcellular_location_section">'Subcellular location'</a> section describes the subcellular compartment where each non-membrane region of a membrane-spanning protein is found.<p><a href='/help/topo_dom' target='_top'>More...</a></p>Topological domaini1 – 21CytoplasmicAdd BLAST21
<p>This subsection of the <a href="http://www.uniprot.org/help/subcellular_location_section">'Subcellular location'</a> section describes the extent of a membrane-spanning region of the protein. It denotes the presence of both alpha-helical transmembrane regions and the membrane spanning regions of beta-barrel transmembrane proteins.<p><a href='/help/transmem' target='_top'>More...</a></p>Transmembranei22 – 42HelicalSequence analysisAdd BLAST21
Topological domaini43 – 646ExtracellularAdd BLAST604
Transmembranei647 – 667HelicalSequence analysisAdd BLAST21
Transmembranei700 – 720HelicalSequence analysisAdd BLAST21
Transmembranei731 – 751HelicalSequence analysisAdd BLAST21
Transmembranei760 – 780HelicalSequence analysisAdd BLAST21
Transmembranei836 – 856HelicalSequence analysisAdd BLAST21
Topological domaini857 – 1376CytoplasmicAdd BLAST520
Transmembranei1377 – 1397HelicalSequence analysisAdd BLAST21
Topological domaini1398 – 1727ExtracellularAdd BLAST330
Transmembranei1728 – 1748HelicalSequence analysisAdd BLAST21
Transmembranei1760 – 1780HelicalSequence analysisAdd BLAST21
Transmembranei1793 – 1813HelicalSequence analysisAdd BLAST21
Transmembranei1832 – 1852HelicalSequence analysisAdd BLAST21
Transmembranei1874 – 1894HelicalSequence analysisAdd BLAST21
Topological domaini1895 – 2273CytoplasmicAdd BLAST379

Keywords - Cellular componenti

Endoplasmic reticulum, Membrane

<p>This section provides information on the disease(s) and phenotype(s) associated with a protein.<p><a href='/help/pathology_and_biotech_section' target='_top'>More...</a></p>Pathology & Biotechi

<p>This subsection of the ‘Pathology and Biotech’ section provides information on the disease(s) associated with genetic variations in a given protein. The information is extracted from the scientific literature and diseases that are also described in the <a href="http://www.ncbi.nlm.nih.gov/sites/entrez?db=omim">OMIM</a> database are represented with a <a href="http://www.uniprot.org/diseases">controlled vocabulary</a> in the following way:<p><a href='/help/involvement_in_disease' target='_top'>More...</a></p>Involvement in diseasei

Stargardt disease 1 (STGD1)19 Publications
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionA common hereditary macular degeneration. It is characterized by decreased central vision, atrophy of the macula and underlying retinal pigment epithelium, and frequent presence of prominent flecks in the posterior pole of the retina.
Related information in OMIM
Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the ‘Sequence’ section describes natural variant(s) of the protein sequence.<p><a href='/help/variant' target='_top'>More...</a></p>Natural variantiVAR_01249413 – 15Missing in STGD1. 1 Publication3
Natural variantiVAR_00839818R → W in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs121909205EnsemblClinVar.1
Natural variantiVAR_00839924R → H in STGD1. Corresponds to variant dbSNP:rs62645958EnsemblClinVar.1
Natural variantiVAR_00840054C → Y in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs150774447EnsemblClinVar.1
Natural variantiVAR_01249558N → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748524EnsemblClinVar.1
Natural variantiVAR_01249660A → E in STGD1. 1 Publication1
Natural variantiVAR_01249760A → T in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61751411EnsemblClinVar.1
Natural variantiVAR_00849260A → V in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs55732384EnsemblClinVar.1
Natural variantiVAR_00840165G → E in STGD1 and CORD3. 3 PublicationsCorresponds to variant dbSNP:rs62654395EnsemblClinVar.1
Natural variantiVAR_01249868P → L in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62654397EnsemblClinVar.1
Natural variantiVAR_01249968P → R in STGD1. Corresponds to variant dbSNP:rs62654397EnsemblClinVar.1
Natural variantiVAR_01250072G → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61751412EnsemblClinVar.1
Natural variantiVAR_00840275C → G in STGD1. Corresponds to variant dbSNP:rs61748526EnsemblClinVar.1
Natural variantiVAR_01250177V → E in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748527EnsemblClinVar.1
Natural variantiVAR_00840396N → D in STGD1. Corresponds to variant dbSNP:rs61748529EnsemblClinVar.1
Natural variantiVAR_00840496N → H in STGD1. Corresponds to variant dbSNP:rs61748529EnsemblClinVar.1
Natural variantiVAR_012502100S → P in STGD1; highly decreased protein abundance; highly decreased ATPase activity; highly decreased phospholipid translocase activity. 1 PublicationCorresponds to variant dbSNP:rs61748530EnsemblClinVar.1
Natural variantiVAR_012504156I → V in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62646863EnsemblClinVar.1
Natural variantiVAR_012505190Q → H in STGD1. 1 PublicationCorresponds to variant dbSNP:rs281865397EnsemblClinVar.1
Natural variantiVAR_008405192A → T in STGD1. Corresponds to variant dbSNP:rs61748535EnsemblClinVar.1
Natural variantiVAR_012506206S → R in STGD1; reduced basal and retinal-stimulated ATP-hydrolysis. 1 PublicationCorresponds to variant dbSNP:rs61748536EnsemblClinVar.1
Natural variantiVAR_008406212R → C in STGD1 and CORD3; common mutation in southern Europe; reduced ATP-binding capacity. 7 PublicationsCorresponds to variant dbSNP:rs61750200EnsemblClinVar.1
Natural variantiVAR_012508220R → C in STGD1. Corresponds to variant dbSNP:rs61748538EnsemblClinVar.1
Natural variantiVAR_012509230C → S in STGD1. 1 PublicationCorresponds to variant dbSNP:rs1057518767EnsemblClinVar.1
Natural variantiVAR_012510244L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62646864EnsemblClinVar.1
Natural variantiVAR_012511247N → S in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62645950EnsemblClinVar.1
Natural variantiVAR_008407249D → G in STGD1. Corresponds to variant dbSNP:rs62646865EnsemblClinVar.1
Natural variantiVAR_008408300T → N in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748544EnsemblClinVar.1
Natural variantiVAR_012512309P → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748545EnsemblClinVar.1
Natural variantiVAR_012513328E → V in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61751419EnsemblClinVar.1
Natural variantiVAR_012514333R → W in STGD1. Corresponds to variant dbSNP:rs61748546EnsemblClinVar.1
Natural variantiVAR_008409336S → C in STGD1. Corresponds to variant dbSNP:rs61748547EnsemblClinVar.1
Natural variantiVAR_008410340Y → D in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748548EnsemblClinVar.1
Natural variantiVAR_012516380N → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748549EnsemblClinVar.1
Natural variantiVAR_008411407A → V in STGD1 and CORD3. Corresponds to variant dbSNP:rs61751264EnsemblClinVar.1
Natural variantiVAR_008412445S → R in STGD1. Corresponds to variant dbSNP:rs61748552EnsemblClinVar.1
Natural variantiVAR_008413471E → K in ARMD2 and STGD1; ATP-binding capacity and retinal stimulation as in wild-type. 1 PublicationCorresponds to variant dbSNP:rs1800548EnsemblClinVar.1
Natural variantiVAR_008414523D → E in STGD1. Corresponds to variant dbSNP:rs62646868EnsemblClinVar.1
Natural variantiVAR_012518525F → C in STGD1. 1 Publication1
Natural variantiVAR_012519537R → C in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748556EnsemblClinVar.1
Natural variantiVAR_008415541L → P in STGD1, FFM and CORD3; reduced ATP-binding capacity; abolishes retinal-stimulated ATP hydrolysis. 5 PublicationsCorresponds to variant dbSNP:rs61751392EnsemblClinVar.1
Natural variantiVAR_012520549A → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748557EnsemblClinVar.1
Natural variantiVAR_012521550G → R in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61748558EnsemblClinVar.1
Natural variantiVAR_008416572R → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61748559EnsemblClinVar.1
Natural variantiVAR_008417572R → Q in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61748559EnsemblClinVar.1
Natural variantiVAR_012523602R → Q in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749410EnsemblClinVar.1
Natural variantiVAR_008418602R → W in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61749409EnsemblClinVar.1
Natural variantiVAR_012524607G → R in STGD1. 3 PublicationsCorresponds to variant dbSNP:rs61749412EnsemblClinVar.1
Natural variantiVAR_012525607G → W in STGD1. Corresponds to variant dbSNP:rs61749412EnsemblClinVar.1
Natural variantiVAR_008419608F → I in STGD1; moderately decreased protein abundance; highly decreased ATPase activity; highly decreased phospholipid translocase activity. 1 PublicationCorresponds to variant dbSNP:rs61752398EnsemblClinVar.1
Natural variantiVAR_012526635Q → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749414EnsemblClinVar.1
Natural variantiVAR_012527636Q → H in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752400EnsemblClinVar.1
Natural variantiVAR_012528643V → M in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749417EnsemblClinVar.1
Natural variantiVAR_008421645D → N in STGD1. Corresponds to variant dbSNP:rs61749418EnsemblClinVar.1
Natural variantiVAR_012529653R → C in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61749420EnsemblClinVar.1
Natural variantiVAR_012530686L → S in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752402EnsemblClinVar.1
Natural variantiVAR_012531716T → M in STGD1. Corresponds to variant dbSNP:rs61749426EnsemblClinVar.1
Natural variantiVAR_012532764C → Y in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749428EnsemblClinVar.1
Natural variantiVAR_012534765S → N in STGD1. Corresponds to variant dbSNP:rs61749429EnsemblClinVar.1
Natural variantiVAR_012533765S → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752404EnsemblClinVar.1
Natural variantiVAR_012535767V → D in STGD1. 3 PublicationsCorresponds to variant dbSNP:rs61751395EnsemblClinVar.1
Natural variantiVAR_012536797L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749432EnsemblClinVar.1
Natural variantiVAR_008422818G → E in ARMD2 and STGD1; reduced ATP-binding capacity. Corresponds to variant dbSNP:rs61750202EnsemblClinVar.1
Natural variantiVAR_008423821W → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749433EnsemblClinVar.1
Natural variantiVAR_012537824I → T in STGD1. 1 Publication1
Natural variantiVAR_012538849V → A in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749435EnsemblClinVar.1
Natural variantiVAR_008424851G → D in STGD1; highly reduced ATP-binding capacity. Corresponds to variant dbSNP:rs61749436EnsemblClinVar.1
Natural variantiVAR_012539854A → T in STGD1. Corresponds to variant dbSNP:rs61749437EnsemblClinVar.1
Natural variantiVAR_008425863G → A in STGD1, FFM and CORD3; mild alteration probably leading to disease phenotype only in combination with a more severe allele; frequent mutation in northern Europe in linkage disequilibrium with the polymorphic variant Q-943; reduced ATP-binding capacity and retinal-stimulated ATP hydrolysis. 5 PublicationsCorresponds to variant dbSNP:rs76157638EnsemblClinVar.1
Natural variantiVAR_012540863Missing in STGD1 and CORD3; reduced ATP-binding capacity and retinal-stimulated ATP hydrolysis. 1 Publication1
Natural variantiVAR_012541873F → L in STGD1. Corresponds to variant dbSNP:rs62642570EnsemblClinVar.1
Natural variantiVAR_012542897T → I in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61749440EnsemblClinVar.1
Natural variantiVAR_008427931V → M in STGD1. 1 PublicationCorresponds to variant dbSNP:rs58331765EnsemblClinVar.1
Natural variantiVAR_012544935V → A in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749444EnsemblClinVar.1
Natural variantiVAR_012545943R → W in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61749446EnsemblClinVar.1
Natural variantiVAR_008429957Q → R in STGD1. Corresponds to variant dbSNP:rs61749448EnsemblClinVar.1
Natural variantiVAR_012546959T → I in STGD1; moderately decreased protein abundance; highly decreased ATPase activity; highly decreased phospholipid translocase activity. 2 PublicationsCorresponds to variant dbSNP:rs61752409EnsemblClinVar.1
Natural variantiVAR_008430965N → S in STGD1; reduced retinal-stimulated ATP hydrolysis; moderately decreased protein abundance; highly decreased ATPase activity; highly decreased phospholipid translocase activity. 3 PublicationsCorresponds to variant dbSNP:rs201471607EnsemblClinVar.1
Natural variantiVAR_012547971T → N in STGD1; highly reduced ATP-binding capacity; abolishes retinal-stimulated ATP hydrolysis. Corresponds to variant dbSNP:rs61749450EnsemblClinVar.1
Natural variantiVAR_012548972T → N in STGD1; unknown pathological significance. 1 PublicationCorresponds to variant dbSNP:rs61749451EnsemblClinVar.1
Natural variantiVAR_012549974S → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs281865400EnsemblClinVar.1
Natural variantiVAR_008431978G → C in STGD1. Corresponds to variant dbSNP:rs61749452EnsemblClinVar.1
Natural variantiVAR_012550989V → A in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61749454EnsemblClinVar.1
Natural variantiVAR_0125521014L → R in STGD1. Corresponds to variant dbSNP:rs61749456EnsemblClinVar.1
Natural variantiVAR_0125531019T → A in STGD1. Corresponds to variant dbSNP:rs61749457EnsemblClinVar.1
Natural variantiVAR_0125541019T → M in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs201855602EnsemblClinVar.1
Natural variantiVAR_0125551022E → K in STGD1. Corresponds to variant dbSNP:rs61749459EnsemblClinVar.1
Natural variantiVAR_0125561031K → E in STGD1. Corresponds to variant dbSNP:rs61750060EnsemblClinVar.1
Natural variantiVAR_0084321036E → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750061EnsemblClinVar.1
Natural variantiVAR_0084331038A → V in STGD1, FFM and CORD3; frequent mutation; reduced ATP-binding and retinal-stimulated ATP hydrolysis. 8 PublicationsCorresponds to variant dbSNP:rs61751374EnsemblClinVar.1
Natural variantiVAR_0125571055R → W in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752412EnsemblClinVar.1
Natural variantiVAR_0125581063S → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752413EnsemblClinVar.1
Natural variantiVAR_0084341071S → L in STGD1; reduced ATP-binding capacity. Corresponds to variant dbSNP:rs61750065EnsemblClinVar.1
Natural variantiVAR_0084351072V → A in STGD1. 1
Natural variantiVAR_0125591087E → D in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752416EnsemblClinVar.1
Natural variantiVAR_0084361087E → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61751398EnsemblClinVar.1
Natural variantiVAR_0125611097R → C in STGD1. 1 Publication1
Natural variantiVAR_0125621108R → C in STGD1 and FFM; reduced ATP-binding capacity. 5 PublicationsCorresponds to variant dbSNP:rs61750120EnsemblClinVar.1
Natural variantiVAR_0125631108R → H in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750121EnsemblClinVar.1
Natural variantiVAR_0125641108R → L in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750121EnsemblClinVar.1
Natural variantiVAR_0084371112T → N in STGD1. Corresponds to variant dbSNP:rs61750122EnsemblClinVar.1
Natural variantiVAR_0084381122E → K in STGD1 and CORD3. 2 PublicationsCorresponds to variant dbSNP:rs61751399EnsemblClinVar.1
Natural variantiVAR_0125651129R → C in STGD1; may predispose to develop retinal toxicity after treatment with chloroquine and hydroxychloroquine. 1 PublicationCorresponds to variant dbSNP:rs779426136EnsemblClinVar.1
Natural variantiVAR_0084391129R → L in ARMD2 and STGD1; also found in patients with fundus flavimaculatus; reduced ATP-binding capacity. 2 PublicationsCorresponds to variant dbSNP:rs1801269EnsemblClinVar.1
Natural variantiVAR_0084401201L → R in STGD1; may predispose to develop retinal toxicity after treatment with chloroquine and hydroxychloroquine. 2 PublicationsCorresponds to variant dbSNP:rs61750126EnsemblClinVar.1
Natural variantiVAR_0084411204D → N in STGD1. Corresponds to variant dbSNP:rs61750127EnsemblClinVar.1
Natural variantiVAR_0125671250L → P in STGD1. Corresponds to variant dbSNP:rs61750128EnsemblClinVar.1
Natural variantiVAR_0125691300R → Q in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750129EnsemblClinVar.1
Natural variantiVAR_0084431380P → L in STGD1; reduced ATP-binding capacity. 3 PublicationsCorresponds to variant dbSNP:rs61750130EnsemblClinVar.1
Natural variantiVAR_0125701388L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750131EnsemblClinVar.1
Natural variantiVAR_0125711399E → K in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs62642573EnsemblClinVar.1
Natural variantiVAR_0084441406H → Y in STGD1. Corresponds to variant dbSNP:rs61750133EnsemblClinVar.1
Natural variantiVAR_0084451408W → L in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750134EnsemblClinVar.1
Natural variantiVAR_0084461408W → R in STGD1; reduced retinal-stimulated ATP hydrolysis. 1 PublicationCorresponds to variant dbSNP:rs61750135EnsemblClinVar.1
Natural variantiVAR_0084481429V → A in STGD1. Corresponds to variant dbSNP:rs61752432EnsemblClinVar.1
Natural variantiVAR_0125721430L → P in STGD1. 1 Publication1
Natural variantiVAR_0084491433V → I in STGD1. 1 PublicationCorresponds to variant dbSNP:rs56357060EnsemblClinVar.1
Natural variantiVAR_0084501439G → D in STGD1. Corresponds to variant dbSNP:rs61750140EnsemblClinVar.1
Natural variantiVAR_0084511440F → S in STGD1. Corresponds to variant dbSNP:rs61750141EnsemblClinVar.1
Natural variantiVAR_0125731440F → V in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61752433EnsemblClinVar.1
Natural variantiVAR_0125741443R → H in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750142EnsemblClinVar.1
Natural variantiVAR_0084521486P → L in STGD1. 3 PublicationsCorresponds to variant dbSNP:rs61750145EnsemblClinVar.1
Natural variantiVAR_0125751488C → F in STGD1. Corresponds to variant dbSNP:rs61750147EnsemblClinVar.1
Natural variantiVAR_0084531488C → R in STGD1 and FFM; reduced retinal-stimulated ATP hydrolysis. 3 PublicationsCorresponds to variant dbSNP:rs61750146EnsemblClinVar.1
Natural variantiVAR_0125761488C → Y in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750147EnsemblClinVar.1
Natural variantiVAR_0084541490C → Y in STGD1 and CORD3; reduced retinal-stimulated ATP hydrolysis. 3 PublicationsCorresponds to variant dbSNP:rs61751402EnsemblClinVar.1
Natural variantiVAR_0125781513Q → R in STGD1. Corresponds to variant dbSNP:rs281865402EnsemblClinVar.1
Natural variantiVAR_0125791525L → P in STGD1. Corresponds to variant dbSNP:rs61750151EnsemblClinVar.1
Natural variantiVAR_0084561526T → M in STGD1; reduced retinal-stimulated ATP hydrolysis. 1 PublicationCorresponds to variant dbSNP:rs61750152EnsemblClinVar.1
Natural variantiVAR_0084571532D → N in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62642574EnsemblClinVar.1
Natural variantiVAR_0125801537T → M in STGD1; moderately decreased protein abundance; moderately decreased ATPase activity; moderately decreased phospholipid translocase activity. 2 PublicationsCorresponds to variant dbSNP:rs62642575EnsemblClinVar.1
Natural variantiVAR_0084581562I → T in STGD1, FFM, ARMD2 and CORD3. 3 PublicationsCorresponds to variant dbSNP:rs1762111EnsemblClinVar.1
Natural variantiVAR_0084601631L → P in STGD1. Corresponds to variant dbSNP:rs61750158EnsemblClinVar.1
Natural variantiVAR_0125831640R → Q in STGD1, FFM and CORD3. 4 PublicationsCorresponds to variant dbSNP:rs61751403EnsemblClinVar.1
Natural variantiVAR_0084611640R → W in STGD1 and CORD3. 3 PublicationsCorresponds to variant dbSNP:rs61751404EnsemblClinVar.1
Natural variantiVAR_0084621652Y → D in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750560EnsemblClinVar.1
Natural variantiVAR_0125841681 – 1685Missing in STGD1; highly reduced ATP-binding capacity. 5
Natural variantiVAR_0125851689S → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61753020EnsemblClinVar.1
Natural variantiVAR_0125861693V → I in STGD1. Corresponds to variant dbSNP:rs61750563EnsemblClinVar.1
Natural variantiVAR_0084631696S → N in STGD1. Corresponds to variant dbSNP:rs61750564EnsemblClinVar.1
Natural variantiVAR_0084641703Q → K in STGD1. 1
Natural variantiVAR_0125871705R → L in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61753021EnsemblClinVar.1
Natural variantiVAR_0084651729L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750567EnsemblClinVar.1
Natural variantiVAR_0125881733M → T in STGD1. 1 PublicationCorresponds to variant dbSNP:rs765563320Ensembl.1
Natural variantiVAR_0125891736S → P in STGD1. Corresponds to variant dbSNP:rs61750568EnsemblClinVar.1
Natural variantiVAR_0125901748G → R in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61753025EnsemblClinVar.1
Natural variantiVAR_0125911761 – 1763Missing in STGD1; highly reduced ATP-binding capacity. 3
Natural variantiVAR_0125921763L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61753028EnsemblClinVar.1
Natural variantiVAR_0125931776P → L in STGD1. 1 PublicationCorresponds to variant dbSNP:rs281865404EnsemblClinVar.1
Natural variantiVAR_0125941780P → A in STGD1. 1 PublicationCorresponds to variant dbSNP:rs121909207EnsemblClinVar.1
Natural variantiVAR_0084661794A → D in STGD1. Corresponds to variant dbSNP:rs61751406EnsemblClinVar.1
Natural variantiVAR_0125951799N → D in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61750574EnsemblClinVar.1
Natural variantiVAR_0125961805N → D in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61753029EnsemblClinVar.1
Natural variantiVAR_0084671820R → P in STGD1. Corresponds to variant dbSNP:rs62646875EnsemblClinVar.1
Natural variantiVAR_0084681838H → Y in STGD1. Corresponds to variant dbSNP:rs62642562EnsemblClinVar.1
Natural variantiVAR_0084691843R → W in STGD1. Corresponds to variant dbSNP:rs62642576EnsemblClinVar.1
Natural variantiVAR_0125981884V → E in STGD1. Corresponds to variant dbSNP:rs62642578EnsemblClinVar.1
Natural variantiVAR_0125991885E → K in STGD1. 1 PublicationCorresponds to variant dbSNP:rs62642563EnsemblClinVar.1
Natural variantiVAR_0084711886G → E in STGD1; highly reduced ATP-binding capacity. Corresponds to variant dbSNP:rs62642579EnsemblClinVar.1
Natural variantiVAR_0084721890Missing in STGD1. 1
Natural variantiVAR_0126001896V → D in STGD1. Corresponds to variant dbSNP:rs61750636EnsemblClinVar.1
Natural variantiVAR_0084731898R → H in STGD1 and ARMD2. 2 PublicationsCorresponds to variant dbSNP:rs1800552EnsemblClinVar.1
Natural variantiVAR_0126021940L → P in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61753033EnsemblClinVar.1
Natural variantiVAR_0084751961G → E in STGD1 and FFM; frequent mutation; may be associated with ARMD2; inhibition of ATP hydrolysis by retinal. 7 PublicationsCorresponds to variant dbSNP:rs1800553EnsemblClinVar.1
Natural variantiVAR_0126041975G → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61753036EnsemblClinVar.1
Natural variantiVAR_0084771977G → S in STGD1 and ARMD2; highly reduced ATP-binding capacity; inhibition of ATP hydrolysis by retinal. 5 PublicationsCorresponds to variant dbSNP:rs61750639EnsemblClinVar.1
Natural variantiVAR_0084782027L → F in STGD1 and FFM; highly reduced ATP-binding capacity. 3 PublicationsCorresponds to variant dbSNP:rs61751408EnsemblClinVar.1
Natural variantiVAR_0084802030R → Q in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61750641EnsemblClinVar.1
Natural variantiVAR_0126052035L → P in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750642EnsemblClinVar.1
Natural variantiVAR_0084952038R → W in STGD1; highly reduced ATP-binding capacity. 1 PublicationCorresponds to variant dbSNP:rs61750643EnsemblClinVar.1
Natural variantiVAR_0084812050V → L in STGD1; may act as a modifier of macular dystrophy in patients who also have a TRP-172 mutation in PRPH2.. 2 PublicationsCorresponds to variant dbSNP:rs41292677EnsemblClinVar.1
Natural variantiVAR_0126082071Y → F in STGD1. 1
Natural variantiVAR_0126092077R → G in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750645EnsemblClinVar.1
Natural variantiVAR_0084822077R → W in STGD1; highly reduced ATP-binding capacity. 2 PublicationsCorresponds to variant dbSNP:rs61750645EnsemblClinVar.1
Natural variantiVAR_0084832096E → K in STGD1; inhibition of ATP hydrolysis by retinal. Corresponds to variant dbSNP:rs61750646EnsemblClinVar.1
Natural variantiVAR_0084842106R → C in STGD1 and FFM; reduced ATP-binding capacity. 1 PublicationCorresponds to variant dbSNP:rs61750648EnsemblClinVar.1
Natural variantiVAR_0126102107R → C in STGD1. 1 PublicationCorresponds to variant dbSNP:rs2297669Ensembl.1
Natural variantiVAR_0084852107R → H in STGD1; may predispose to develop retinal toxicity after treatment with chloroquine and hydroxychloroquine. 6 PublicationsCorresponds to variant dbSNP:rs62642564EnsemblClinVar.1
Natural variantiVAR_0084862128H → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750651EnsemblClinVar.1
Natural variantiVAR_0084872131E → K in STGD1. Corresponds to variant dbSNP:rs61750652EnsemblClinVar.1
Natural variantiVAR_0084882139R → W in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750653EnsemblClinVar.1
Natural variantiVAR_0126122149R → L in STGD1. Corresponds to variant dbSNP:rs61750655EnsemblClinVar.1
Natural variantiVAR_0126132150C → R in STGD1. 1 PublicationCorresponds to variant dbSNP:rs61750656EnsemblClinVar.1
Natural variantiVAR_0084892150C → Y in STGD1 and CORD3. 3 PublicationsCorresponds to variant dbSNP:rs61751384EnsemblClinVar.1
Natural variantiVAR_0084902160K → R in STGD1. Corresponds to variant dbSNP:rs281865405EnsemblClinVar.1
Natural variantiVAR_0126152229L → P in STGD1. Corresponds to variant dbSNP:rs61750659EnsemblClinVar.1
Natural variantiVAR_0126162241L → V in STGD1. 2 PublicationsCorresponds to variant dbSNP:rs61748521EnsemblClinVar.1
Natural variantiVAR_0126172263R → L in STGD1. Corresponds to variant dbSNP:rs281865407EnsemblClinVar.1
Fundus flavimaculatus (FFM)3 Publications
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionAutosomal recessive retinal disorder very similar to Stargardt disease. In contrast to Stargardt disease, FFM is characterized by later onset and slowly progressive course.
Related information in OMIM
Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_01249311L → P in FFM. 1 PublicationCorresponds to variant dbSNP:rs62645946EnsemblClinVar.1
Natural variantiVAR_012515339W → G in FFM. 1 PublicationCorresponds to variant dbSNP:rs61751420EnsemblClinVar.1
Natural variantiVAR_012545943R → W in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61749446EnsemblClinVar.1
Natural variantiVAR_012551991G → R in FFM. 1 PublicationCorresponds to variant dbSNP:rs61749455EnsemblClinVar.1
Natural variantiVAR_0125601091G → E in FFM. 1 PublicationCorresponds to variant dbSNP:rs61752417EnsemblClinVar.1
Natural variantiVAR_0125621108R → C in STGD1 and FFM; reduced ATP-binding capacity. 5 PublicationsCorresponds to variant dbSNP:rs61750120EnsemblClinVar.1
Natural variantiVAR_0125681253T → M in FFM; unknown pathological significance. 1 PublicationCorresponds to variant dbSNP:rs61752424EnsemblClinVar.1
Natural variantiVAR_0084531488C → R in STGD1 and FFM; reduced retinal-stimulated ATP hydrolysis. 3 PublicationsCorresponds to variant dbSNP:rs61750146EnsemblClinVar.1
Natural variantiVAR_0125771508G → C in FFM. 1 Publication1
Natural variantiVAR_0126021940L → P in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61753033EnsemblClinVar.1
Natural variantiVAR_0084751961G → E in STGD1 and FFM; frequent mutation; may be associated with ARMD2; inhibition of ATP hydrolysis by retinal. 7 PublicationsCorresponds to variant dbSNP:rs1800553EnsemblClinVar.1
Natural variantiVAR_0084761970L → F in ARMD2 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs28938473EnsemblClinVar.1
Natural variantiVAR_0126031971L → R in FFM; highly reduced ATP-binding capacity; abolishes basal and retinal-stimulated ATP hydrolysis. 1 PublicationCorresponds to variant dbSNP:rs61753034EnsemblClinVar.1
Natural variantiVAR_0084782027L → F in STGD1 and FFM; highly reduced ATP-binding capacity. 3 PublicationsCorresponds to variant dbSNP:rs61751408EnsemblClinVar.1
Natural variantiVAR_0084802030R → Q in STGD1 and FFM. 2 PublicationsCorresponds to variant dbSNP:rs61750641EnsemblClinVar.1
Natural variantiVAR_0084842106R → C in STGD1 and FFM; reduced ATP-binding capacity. 1 PublicationCorresponds to variant dbSNP:rs61750648EnsemblClinVar.1
Macular degeneration, age-related, 2 (ARMD2)2 Publications
Disease susceptibility is associated with variations affecting the gene represented in this entry.
Disease descriptionA form of age-related macular degeneration, a multifactorial eye disease and the most common cause of irreversible vision loss in the developed world. In most patients, the disease is manifest as ophthalmoscopically visible yellowish accumulations of protein and lipid that lie beneath the retinal pigment epithelium and within an elastin-containing structure known as Bruch membrane.
Related information in OMIM
Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_008413471E → K in ARMD2 and STGD1; ATP-binding capacity and retinal stimulation as in wild-type. 1 PublicationCorresponds to variant dbSNP:rs1800548EnsemblClinVar.1
Natural variantiVAR_067427762A → E in ARMD2. 1 Publication1
Natural variantiVAR_008422818G → E in ARMD2 and STGD1; reduced ATP-binding capacity. Corresponds to variant dbSNP:rs61750202EnsemblClinVar.1
Natural variantiVAR_0084391129R → L in ARMD2 and STGD1; also found in patients with fundus flavimaculatus; reduced ATP-binding capacity. 2 PublicationsCorresponds to variant dbSNP:rs1801269EnsemblClinVar.1
Natural variantiVAR_0084471428T → M in ARMD2. Corresponds to variant dbSNP:rs1800549EnsemblClinVar.1
Natural variantiVAR_0084551517R → S in ARMD2. Corresponds to variant dbSNP:rs1800550EnsemblClinVar.1
Natural variantiVAR_0084591578G → R in ARMD2. Corresponds to variant dbSNP:rs1800551EnsemblClinVar.1
Natural variantiVAR_0674281724W → C in ARMD2. 1 Publication1
Natural variantiVAR_0084731898R → H in STGD1 and ARMD2. 2 Publications