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Entry version 176 (16 Oct 2019)
Sequence version 2 (24 Jan 2001)
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Protein

Thiamine transporter 1

Gene

SLC19A2

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

High-affinity transporter for the intake of thiamine.2 Publications

<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

Biological processTransport

Enzyme and pathway databases

Reactome - a knowledgebase of biological pathways and processes

More...
Reactomei
R-HSA-196819 Vitamin B1 (thiamin) metabolism

SABIO-RK: Biochemical Reaction Kinetics Database

More...
SABIO-RKi
O60779

Protein family/group databases

Transport Classification Database

More...
TCDBi
2.A.48.1.2 the reduced folate carrier (rfc) family

<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:
Thiamine transporter 1
Short name:
ThTr-1
Short name:
ThTr1
Alternative name(s):
Solute carrier family 19 member 2
Thiamine carrier 1
Short name:
TC1
<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:SLC19A2
Synonyms:THT1, TRMA
<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:10938 SLC19A2

Online Mendelian Inheritance in Man (OMIM)

More...
MIMi
603941 gene

neXtProt; the human protein knowledge platform

More...
neXtProti
NX_O60779

<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 – 28CytoplasmicSequence analysisAdd BLAST28
<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>Transmembranei29 – 46HelicalSequence analysisAdd BLAST18
Topological domaini47 – 72ExtracellularSequence analysisAdd BLAST26
Transmembranei73 – 91HelicalSequence analysisAdd BLAST19
Topological domaini92 – 99CytoplasmicSequence analysis8
Transmembranei100 – 118HelicalSequence analysisAdd BLAST19
Topological domaini119 – 128ExtracellularSequence analysis10
Transmembranei129 – 149HelicalSequence analysisAdd BLAST21
Topological domaini150 – 165CytoplasmicSequence analysisAdd BLAST16
Transmembranei166 – 185HelicalSequence analysisAdd BLAST20
Topological domaini186 – 191ExtracellularSequence analysis6
Transmembranei192 – 208HelicalSequence analysisAdd BLAST17
Topological domaini209 – 285CytoplasmicSequence analysisAdd BLAST77
Transmembranei286 – 310HelicalSequence analysisAdd BLAST25
Topological domaini311 – 337ExtracellularSequence analysisAdd BLAST27
Transmembranei338 – 354HelicalSequence analysisAdd BLAST17
Topological domaini355 – 363CytoplasmicSequence analysis9
Transmembranei364 – 380HelicalSequence analysisAdd BLAST17
Topological domaini381 – 386ExtracellularSequence analysis6
Transmembranei387 – 409HelicalSequence analysisAdd BLAST23
Topological domaini410 – 419CytoplasmicSequence analysis10
Transmembranei420 – 443HelicalSequence analysisAdd BLAST24
Topological domaini444 – 455ExtracellularSequence analysisAdd BLAST12
Transmembranei456 – 479HelicalSequence analysisAdd BLAST24
Topological domaini480 – 497CytoplasmicSequence analysisAdd BLAST18

Keywords - Cellular componenti

Cell membrane, 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

Thiamine-responsive megaloblastic anemia syndrome (TRMA)2 Publications
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionAn autosomal recessive disease characterized by megaloblastic anemia, diabetes mellitus, and sensorineural deafness. Onset is typically between infancy and adolescence, but all of the cardinal findings are often not present initially. The anemia, and sometimes the diabetes, improves with high doses of thiamine. Other more variable features include optic atrophy, congenital heart defects, short stature, and stroke.
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_01024993D → H in TRMA. 1 Publication1
Natural variantiVAR_010250143S → F in TRMA. 1 PublicationCorresponds to variant dbSNP:rs761957186EnsemblClinVar.1
Natural variantiVAR_010248172G → D in TRMA. 1 PublicationCorresponds to variant dbSNP:rs28937595EnsemblClinVar.1

Keywords - Diseasei

Deafness, Diabetes mellitus, Disease mutation

Organism-specific databases

DisGeNET

More...
DisGeNETi
10560

GeneReviews a resource of expert-authored, peer-reviewed disease descriptions.

More...
GeneReviewsi
SLC19A2

MalaCards human disease database

More...
MalaCardsi
SLC19A2
MIMi249270 phenotype

Open Targets

More...
OpenTargetsi
ENSG00000117479

Orphanet; a database dedicated to information on rare diseases and orphan drugs

More...
Orphaneti
49827 Thiamine-responsive megaloblastic anemia syndrome

The Pharmacogenetics and Pharmacogenomics Knowledge Base

More...
PharmGKBi
PA35825

Miscellaneous databases

Pharos NIH Druggable Genome Knowledgebase

More...
Pharosi
O60779

Chemistry databases

ChEMBL database of bioactive drug-like small molecules

More...
ChEMBLi
CHEMBL3079

Drug and drug target database

More...
DrugBanki
DB00152 Thiamine

DrugCentral

More...
DrugCentrali
O60779

Polymorphism and mutation databases

BioMuta curated single-nucleotide variation and disease association database

More...
BioMutai
SLC19A2

<p>This section describes post-translational modifications (PTMs) and/or processing events.<p><a href='/help/ptm_processing_section' target='_top'>More...</a></p>PTM / Processingi

Molecule processing

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the ‘PTM / Processing’ section describes the extent of a polypeptide chain in the mature protein following processing.<p><a href='/help/chain' target='_top'>More...</a></p>ChainiPRO_00001786631 – 497Thiamine transporter 1Add BLAST497

Amino acid modifications

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the ‘PTM / Processing’ section specifies the position and type of each modified residue excluding <a href="http://www.uniprot.org/manual/lipid">lipids</a>, <a href="http://www.uniprot.org/manual/carbohyd">glycans</a> and <a href="http://www.uniprot.org/manual/crosslnk">protein cross-links</a>.<p><a href='/help/mod_res' target='_top'>More...</a></p>Modified residuei1N-acetylmethionineCombined sources1
<p>This subsection of the <a href="http://www.uniprot.org/help/ptm_processing_section">PTM / Processing</a> section specifies the position and type of each covalently attached glycan group (mono-, di-, or polysaccharide).<p><a href='/help/carbohyd' target='_top'>More...</a></p>Glycosylationi63N-linked (GlcNAc...) asparagineSequence analysis1
Modified residuei222PhosphoserineCombined sources1
Glycosylationi314N-linked (GlcNAc...) asparagineSequence analysis1

Keywords - PTMi

Acetylation, Glycoprotein, Phosphoprotein

Proteomic databases

Encyclopedia of Proteome Dynamics

More...
EPDi
O60779

jPOST - Japan Proteome Standard Repository/Database

More...
jPOSTi
O60779

MassIVE - Mass Spectrometry Interactive Virtual Environment

More...
MassIVEi
O60779

MaxQB - The MaxQuant DataBase

More...
MaxQBi
O60779

PaxDb, a database of protein abundance averages across all three domains of life

More...
PaxDbi
O60779

PeptideAtlas

More...
PeptideAtlasi
O60779

PRoteomics IDEntifications database

More...
PRIDEi
O60779

ProteomicsDB: a multi-organism proteome resource

More...
ProteomicsDBi
49594 [O60779-1]
49595 [O60779-2]

PTM databases

iPTMnet integrated resource for PTMs in systems biology context

More...
iPTMneti
O60779

Comprehensive resource for the study of protein post-translational modifications (PTMs) in human, mouse and rat.

More...
PhosphoSitePlusi
O60779

<p>This section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms.<p><a href='/help/expression_section' target='_top'>More...</a></p>Expressioni

<p>This subsection of the ‘Expression’ section provides information on the expression of a gene at the mRNA or protein level in cells or in tissues of multicellular organisms. By default, the information is derived from experiments at the mRNA level, unless specified ‘at protein level’. <br></br>Examples: <a href="http://www.uniprot.org/uniprot/P92958#expression">P92958</a>, <a href="http://www.uniprot.org/uniprot/Q8TDN4#expression">Q8TDN4</a>, <a href="http://www.uniprot.org/uniprot/O14734#expression">O14734</a><p><a href='/help/tissue_specificity' target='_top'>More...</a></p>Tissue specificityi

Ubiquitous; most abundant in skeletal and cardiac muscle. Medium expression in placenta, heart, liver and kidney, low in lung.2 Publications

Gene expression databases

Bgee dataBase for Gene Expression Evolution

More...
Bgeei
ENSG00000117479 Expressed in 219 organ(s), highest expression level in secondary oocyte

ExpressionAtlas, Differential and Baseline Expression

More...
ExpressionAtlasi
O60779 baseline and differential

Genevisible search portal to normalized and curated expression data from Genevestigator

More...
Genevisiblei
O60779 HS

Organism-specific databases

Human Protein Atlas

More...
HPAi
HPA006119
HPA016599

<p>This section provides information on the quaternary structure of a protein and on interaction(s) with other proteins or protein complexes.<p><a href='/help/interaction_section' target='_top'>More...</a></p>Interactioni

Protein-protein interaction databases

The Biological General Repository for Interaction Datasets (BioGrid)

More...
BioGridi
115811, 42 interactors

Protein interaction database and analysis system

More...
IntActi
O60779, 29 interactors

STRING: functional protein association networks

More...
STRINGi
9606.ENSP00000236137

Chemistry databases

BindingDB database of measured binding affinities

More...
BindingDBi
O60779

<p>This section provides information on sequence similarities with other proteins and the domain(s) present in a protein.<p><a href='/help/family_and_domains_section' target='_top'>More...</a></p>Family & Domainsi

<p>This subsection of the ‘Family and domains’ section provides information about the sequence similarity with other proteins.<p><a href='/help/sequence_similarities' target='_top'>More...</a></p>Sequence similaritiesi

Keywords - Domaini

Transmembrane, Transmembrane helix

Phylogenomic databases

evolutionary genealogy of genes: Non-supervised Orthologous Groups

More...
eggNOGi
KOG3810 Eukaryota
ENOG410XT34 LUCA

Ensembl GeneTree

More...
GeneTreei
ENSGT00950000183022

InParanoid: Eukaryotic Ortholog Groups

More...
InParanoidi
O60779

KEGG Orthology (KO)

More...
KOi
K14610

Identification of Orthologs from Complete Genome Data

More...
OMAi
VCYSSRP

Database of Orthologous Groups

More...
OrthoDBi
795242at2759

Database for complete collections of gene phylogenies

More...
PhylomeDBi
O60779

TreeFam database of animal gene trees

More...
TreeFami
TF313684

Family and domain databases

Integrated resource of protein families, domains and functional sites

More...
InterProi
View protein in InterPro
IPR002666 Folate_carrier
IPR036259 MFS_trans_sf
IPR028338 ThTr-1

The PANTHER Classification System

More...
PANTHERi
PTHR10686 PTHR10686, 1 hit

Pfam protein domain database

More...
Pfami
View protein in Pfam
PF01770 Folate_carrier, 1 hit

PIRSF; a whole-protein classification database

More...
PIRSFi
PIRSF028739 Folate_carrier, 1 hit
PIRSF500794 Thiamine_transporter_1, 1 hit

Superfamily database of structural and functional annotation

More...
SUPFAMi
SSF103473 SSF103473, 1 hit

<p>This section displays by default the canonical protein sequence and upon request all isoforms described in the entry. It also includes information pertinent to the sequence(s), including <a href="http://www.uniprot.org/help/sequence_length">length</a> and <a href="http://www.uniprot.org/help/sequences">molecular weight</a>. The information is filed in different subsections. The current subsections and their content are listed below:<p><a href='/help/sequences_section' target='_top'>More...</a></p>Sequences (2+)i

<p>This subsection of the <a href="http://www.uniprot.org/help/sequences_section">Sequence</a> section indicates if the <a href="http://www.uniprot.org/help/canonical_and_isoforms">canonical sequence</a> displayed by default in the entry is complete or not.<p><a href='/help/sequence_status' target='_top'>More...</a></p>Sequence statusi: Complete.

This entry describes 2 <p>This subsection of the ‘Sequence’ section lists the alternative protein sequences (isoforms) that can be generated from the same gene by a single or by the combination of up to four biological events (alternative promoter usage, alternative splicing, alternative initiation and ribosomal frameshifting). Additionally, this section gives relevant information on each alternative protein isoform.<p><a href='/help/alternative_products' target='_top'>More...</a></p> isoformsi produced by alternative splicing. AlignAdd to basket

This entry has 2 described isoforms and 1 potential isoform that is computationally mapped.Show allAlign All

Isoform 1 (identifier: O60779-1) [UniParc]FASTAAdd to basket

This isoform has been chosen as the <div> <p><b>What is the canonical sequence?</b><p><a href='/help/canonical_and_isoforms' target='_top'>More...</a></p>canonicali sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry.

« Hide
        10         20         30         40         50
MDVPGPVSRR AAAAAATVLL RTARVRRECW FLPTALLCAY GFFASLRPSE
60 70 80 90 100
PFLTPYLLGP DKNLTEREVF NEIYPVWTYS YLVLLFPVFL ATDYLRYKPV
110 120 130 140 150
VLLQGLSLIV TWFMLLYAQG LLAIQFLEFF YGIATATEIA YYSYIYSVVD
160 170 180 190 200
LGMYQKVTSY CRSATLVGFT VGSVLGQILV SVAGWSLFSL NVISLTCVSV
210 220 230 240 250
AFAVAWFLPM PQKSLFFHHI PSTCQRVNGI KVQNGGIVTD TPASNHLPGW
260 270 280 290 300
EDIESKIPLN MEEPPVEEPE PKPDRLLVLK VLWNDFLMCY SSRPLLCWSV
310 320 330 340 350
WWALSTCGYF QVVNYTQGLW EKVMPSRYAA IYNGGVEAVS TLLGAVAVFA
360 370 380 390 400
VGYIKISWST WGEMTLSLFS LLIAAAVYIM DTVGNIWVCY ASYVVFRIIY
410 420 430 440 450
MLLITIATFQ IAANLSMERY ALVFGVNTFI ALALQTLLTL IVVDASGLGL
460 470 480 490
EITTQFLIYA SYFALIAVVF LASGAVSVMK KCRKLEDPQS SSQVTTS
Length:497
Mass (Da):55,400
Last modified:January 24, 2001 - v2
<p>The checksum is a form of redundancy check that is calculated from the sequence. It is useful for tracking sequence updates.</p> <p>It should be noted that while, in theory, two different sequences could have the same checksum value, the likelihood that this would happen is extremely low.</p> <p>However UniProtKB may contain entries with identical sequences in case of multiple genes (paralogs).</p> <p>The checksum is computed as the sequence 64-bit Cyclic Redundancy Check value (CRC64) using the generator polynomial: x<sup>64</sup> + x<sup>4</sup> + x<sup>3</sup> + x + 1. The algorithm is described in the ISO 3309 standard. </p> <p class="publication">Press W.H., Flannery B.P., Teukolsky S.A. and Vetterling W.T.<br /> <strong>Cyclic redundancy and other checksums</strong><br /> <a href="http://www.nrbook.com/b/bookcpdf.php">Numerical recipes in C 2nd ed., pp896-902, Cambridge University Press (1993)</a>)</p> Checksum:i87A993E2B6FBFE96
GO
Isoform 2 (identifier: O60779-2) [UniParc]FASTAAdd to basket

The sequence of this isoform differs from the canonical sequence as follows:
     69-269: Missing.

Show »
Length:296
Mass (Da):32,858
Checksum:iA8C5CDFF6D54540C
GO

<p>In eukaryotic reference proteomes, unreviewed entries that are likely to belong to the same gene are computationally mapped, based on gene identifiers from Ensembl, EnsemblGenomes and model organism databases.<p><a href='/help/gene_centric_isoform_mapping' target='_top'>More...</a></p>Computationally mapped potential isoform sequencesi

There is 1 potential isoform mapped to this entry.BLASTAlignShow allAdd to basket
EntryEntry nameProtein names
Gene namesLengthAnnotation
A0A2R8Y5B5A0A2R8Y5B5_HUMAN
Solute carrier family 19 (Thiamine ...
SLC19A2 hCG_38014
464Annotation score:

Annotation score:1 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>

<p>This subsection of the ‘Sequence’ section reports difference(s) between the protein sequence shown in the UniProtKB entry and other available protein sequences derived from the same gene.<p><a href='/help/sequence_caution' target='_top'>More...</a></p>Sequence cautioni

The sequence BAG64936 differs from that shown. Reason: Erroneous initiation.Curated

Natural variant

Feature keyPosition(s)DescriptionActionsGraphical viewLength
Natural variantiVAR_01024993D → H in TRMA. 1 Publication1
Natural variantiVAR_010250143S → F in TRMA. 1 PublicationCorresponds to variant dbSNP:rs761957186EnsemblClinVar.1
Natural variantiVAR_010248172G → D in TRMA. 1 PublicationCorresponds to variant dbSNP:rs28937595EnsemblClinVar.1

Alternative sequence

Feature keyPosition(s)DescriptionActionsGraphical viewLength
<p>This subsection of the ‘Sequence’ section describes the sequence of naturally occurring alternative protein isoform(s). The changes in the amino acid sequence may be due to alternative splicing, alternative promoter usage, alternative initiation, or ribosomal frameshifting.<p><a href='/help/var_seq' target='_top'>More...</a></p>Alternative sequenceiVSP_03646769 – 269Missing in isoform 2. 1 PublicationAdd BLAST201

Sequence databases

Select the link destinations:

EMBL nucleotide sequence database

More...
EMBLi

GenBank nucleotide sequence database

More...
GenBanki

DNA Data Bank of Japan; a nucleotide sequence database

More...
DDBJi
Links Updated
AF160812 mRNA Translation: AAF15129.1
AJ238413 Genomic DNA Translation: CAB50771.1
AJ237724 mRNA Translation: CAB50770.1
AF135488 mRNA Translation: AAD45985.1
AF158233 Genomic DNA Translation: AAD51280.1 Sequence problems.
AF160186 Genomic DNA Translation: AAD51283.1 Sequence problems.
AF160756 Genomic DNA Translation: AAD54242.1
AF153330 mRNA Translation: AAD43534.1
AF272359 mRNA Translation: AAK54468.1
AK304021 mRNA Translation: BAG64936.1 Different initiation.
AK313779 mRNA Translation: BAG36517.1
AK316465 mRNA Translation: BAH14836.1
AL021068 Genomic DNA No translation available.
CH471067 Genomic DNA Translation: EAW90843.1
CH471067 Genomic DNA Translation: EAW90846.1
BC018514 mRNA Translation: AAH18514.1

The Consensus CDS (CCDS) project

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CCDSi
CCDS1280.1 [O60779-1]
CCDS81398.1 [O60779-2]

NCBI Reference Sequences

More...
RefSeqi
NP_001306596.1, NM_001319667.1 [O60779-2]
NP_008927.1, NM_006996.2 [O60779-1]

Genome annotation databases

Ensembl eukaryotic genome annotation project

More...
Ensembli
ENST00000236137; ENSP00000236137; ENSG00000117479 [O60779-1]
ENST00000367804; ENSP00000356778; ENSG00000117479 [O60779-2]

Database of genes from NCBI RefSeq genomes

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GeneIDi
10560

KEGG: Kyoto Encyclopedia of Genes and Genomes

More...
KEGGi
hsa:10560

UCSC genome browser

More...
UCSCi
uc001gge.5 human [O60779-1]

Keywords - Coding sequence diversityi

Alternative splicing

<p>This section provides links to proteins that are similar to the protein sequence(s) described in this entry at different levels of sequence identity thresholds (100%, 90% and 50%) based on their membership in UniProt Reference Clusters (<a href="http://www.uniprot.org/help/uniref">UniRef</a>).<p><a href='/help/similar_proteins_section' target='_top'>More...</a></p>Similar proteinsi

<p>This section is used to point to information related to entries and found in data collections other than UniProtKB.<p><a href='/help/cross_references_section' target='_top'>More...</a></p>Cross-referencesi

Sequence databases

Select the link destinations:
EMBLi
GenBanki
DDBJi
Links Updated
AF160812 mRNA Translation: AAF15129.1
AJ238413 Genomic DNA Translation: CAB50771.1
AJ237724 mRNA Translation: CAB50770.1
AF135488 mRNA Translation: AAD45985.1
AF158233 Genomic DNA Translation: AAD51280.1 Sequence problems.
AF160186 Genomic DNA Translation: AAD51283.1 Sequence problems.
AF160756 Genomic DNA Translation: AAD54242.1
AF153330 mRNA Translation: AAD43534.1
AF272359 mRNA Translation: AAK54468.1
AK304021 mRNA Translation: BAG64936.1 Different initiation.
AK313779 mRNA Translation: BAG36517.1
AK316465 mRNA Translation: BAH14836.1
AL021068 Genomic DNA No translation available.
CH471067 Genomic DNA Translation: EAW90843.1
CH471067 Genomic DNA Translation: EAW90846.1
BC018514 mRNA Translation: AAH18514.1
CCDSiCCDS1280.1 [O60779-1]
CCDS81398.1 [O60779-2]
RefSeqiNP_001306596.1, NM_001319667.1 [O60779-2]
NP_008927.1, NM_006996.2 [O60779-1]

3D structure databases

Database of comparative protein structure models

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ModBasei
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SWISS-MODEL Interactive Workspace

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SWISS-MODEL-Workspacei
Submit a new modelling project...

Protein-protein interaction databases

BioGridi115811, 42 interactors
IntActiO60779, 29 interactors
STRINGi9606.ENSP00000236137

Chemistry databases

BindingDBiO60779
ChEMBLiCHEMBL3079
DrugBankiDB00152 Thiamine
DrugCentraliO60779

Protein family/group databases

TCDBi2.A.48.1.2 the reduced folate carrier (rfc) family

PTM databases

iPTMnetiO60779
PhosphoSitePlusiO60779

Polymorphism and mutation databases

BioMutaiSLC19A2

Proteomic databases

EPDiO60779
jPOSTiO60779
MassIVEiO60779
MaxQBiO60779
PaxDbiO60779
PeptideAtlasiO60779
PRIDEiO60779
ProteomicsDBi49594 [O60779-1]
49595 [O60779-2]

Genome annotation databases

EnsembliENST00000236137; ENSP00000236137; ENSG00000117479 [O60779-1]
ENST00000367804; ENSP00000356778; ENSG00000117479 [O60779-2]
GeneIDi10560
KEGGihsa:10560
UCSCiuc001gge.5 human [O60779-1]

Organism-specific databases

Comparative Toxicogenomics Database

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CTDi
10560
DisGeNETi10560

GeneCards: human genes, protein and diseases

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GeneCardsi
SLC19A2
GeneReviewsiSLC19A2
HGNCiHGNC:10938 SLC19A2
HPAiHPA006119
HPA016599
MalaCardsiSLC19A2
MIMi249270 phenotype
603941 gene
neXtProtiNX_O60779
OpenTargetsiENSG00000117479
Orphaneti49827 Thiamine-responsive megaloblastic anemia syndrome
PharmGKBiPA35825

GenAtlas: human gene database

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GenAtlasi
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Phylogenomic databases

eggNOGiKOG3810 Eukaryota
ENOG410XT34 LUCA
GeneTreeiENSGT00950000183022
InParanoidiO60779
KOiK14610
OMAiVCYSSRP
OrthoDBi795242at2759
PhylomeDBiO60779
TreeFamiTF313684

Enzyme and pathway databases

ReactomeiR-HSA-196819 Vitamin B1 (thiamin) metabolism
SABIO-RKiO60779

Miscellaneous databases

ChiTaRS: a database of human, mouse and fruit fly chimeric transcripts and RNA-sequencing data

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ChiTaRSi
SLC19A2 human

The Gene Wiki collection of pages on human genes and proteins

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GeneWikii
SLC19A2

Database of phenotypes from RNA interference screens in Drosophila and Homo sapiens

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GenomeRNAii
10560
PharosiO60779

Protein Ontology

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PROi
PR:O60779

The Stanford Online Universal Resource for Clones and ESTs

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SOURCEi
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Gene expression databases

BgeeiENSG00000117479 Expressed in 219 organ(s), highest expression level in secondary oocyte
ExpressionAtlasiO60779 baseline and differential
GenevisibleiO60779 HS

Family and domain databases

InterProiView protein in InterPro
IPR002666 Folate_carrier
IPR036259 MFS_trans_sf
IPR028338 ThTr-1
PANTHERiPTHR10686 PTHR10686, 1 hit
PfamiView protein in Pfam
PF01770 Folate_carrier, 1 hit
PIRSFiPIRSF028739 Folate_carrier, 1 hit
PIRSF500794 Thiamine_transporter_1, 1 hit
SUPFAMiSSF103473 SSF103473, 1 hit

ProtoNet; Automatic hierarchical classification of proteins

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ProtoNeti
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MobiDB: a database of protein disorder and mobility annotations

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MobiDBi
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<p>This section provides general information on the entry.<p><a href='/help/entry_information_section' target='_top'>More...</a></p>Entry informationi

<p>This subsection of the ‘Entry information’ section provides a mnemonic identifier for a UniProtKB entry, but it is not a stable identifier. Each reviewed entry is assigned a unique entry name upon integration into UniProtKB/Swiss-Prot.<p><a href='/help/entry_name' target='_top'>More...</a></p>Entry nameiS19A2_HUMAN
<p>This subsection of the ‘Entry information’ section provides one or more accession number(s). These are stable identifiers and should be used to cite UniProtKB entries. Upon integration into UniProtKB, each entry is assigned a unique accession number, which is called ‘Primary (citable) accession number’.<p><a href='/help/accession_numbers' target='_top'>More...</a></p>AccessioniPrimary (citable) accession number: O60779
Secondary accession number(s): B2R9H0
, B4E1X4, Q8WV87, Q9UBL7, Q9UKJ2, Q9UN31, Q9UN43
<p>This subsection of the ‘Entry information’ section shows the date of integration of the entry into UniProtKB, the date of the last sequence update and the date of the last annotation modification (‘Last modified’). The version number for both the entry and the <a href="http://www.uniprot.org/help/canonical_and_isoforms">canonical sequence</a> are also displayed.<p><a href='/help/entry_history' target='_top'>More...</a></p>Entry historyiIntegrated into UniProtKB/Swiss-Prot: July 15, 1999
Last sequence update: January 24, 2001
Last modified: October 16, 2019
This is version 176 of the entry and version 2 of the sequence. See complete history.
<p>This subsection of the ‘Entry information’ section indicates whether the entry has been manually annotated and reviewed by UniProtKB curators or not, in other words, if the entry belongs to the Swiss-Prot section of UniProtKB (<strong>reviewed</strong>) or to the computer-annotated TrEMBL section (<strong>unreviewed</strong>).<p><a href='/help/entry_status' target='_top'>More...</a></p>Entry statusiReviewed (UniProtKB/Swiss-Prot)
Annotation programChordata Protein Annotation Program
DisclaimerAny medical or genetic information present in this entry is provided for research, educational and informational purposes only. It is not in any way intended to be used as a substitute for professional medical advice, diagnosis, treatment or care.

<p>This section contains any relevant information that doesn’t fit in any other defined sections<p><a href='/help/miscellaneous_section' target='_top'>More...</a></p>Miscellaneousi

Keywords - Technical termi

Complete proteome, Reference proteome

Documents

  1. SIMILARITY comments
    Index of protein domains and families
  2. Human polymorphisms and disease mutations
    Index of human polymorphisms and disease mutations
  3. MIM cross-references
    Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot
  4. Human chromosome 1
    Human chromosome 1: entries, gene names and cross-references to MIM
  5. Human entries with polymorphisms or disease mutations
    List of human entries with polymorphisms or disease mutations
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