UniProtKB - Q9Y6Y1 (CMTA1_HUMAN)
Protein
Calmodulin-binding transcription activator 1
Gene
CAMTA1
Organism
Homo sapiens (Human)
Status
Functioni
Transcriptional activator. May act as a tumor suppressor.2 Publications
Miscellaneous
A very small segment of 1p36 located within CAMTA1 is deleted in all oligodendroglial tumors with 1p LOH. This minimal deleted region (MDR) also overlaps the neuroblastoma 1p36 MDR. CAMTA1 shows no evidence of inactivation by somatic mutations.
Regions
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
DNA bindingi | 63 – 188 | CG-1PROSITE-ProRule annotationAdd BLAST | 126 |
GO - Molecular functioni
- DNA-binding transcription factor activity, RNA polymerase II-specific Source: NTNU_SB
- sequence-specific DNA binding Source: GO_Central
GO - Biological processi
- neuromuscular process controlling balance Source: Ensembl
- positive regulation of calcineurin-NFAT signaling cascade Source: BHF-UCL
- positive regulation of protein dephosphorylation Source: BHF-UCL
- positive regulation of transcription by RNA polymerase II Source: GO_Central
Keywordsi
Molecular function | Activator |
Biological process | Transcription, Transcription regulation |
Enzyme and pathway databases
SIGNORi | Q9Y6Y1 |
Names & Taxonomyi
Protein namesi | Recommended name: Calmodulin-binding transcription activator 1 |
Gene namesi | Name:CAMTA1 Synonyms:KIAA0833 ORF Names:MSTP023 |
Organismi | Homo sapiens (Human) |
Taxonomic identifieri | 9606 [NCBI] |
Taxonomic lineagei | Eukaryota › Metazoa › Chordata › Craniata › Vertebrata › Euteleostomi › Mammalia › Eutheria › Euarchontoglires › Primates › Haplorrhini › Catarrhini › Hominidae › Homo |
Proteomesi |
|
Organism-specific databases
HGNCi | HGNC:18806 CAMTA1 |
MIMi | 611501 gene |
neXtProti | NX_Q9Y6Y1 |
Pathology & Biotechi
Involvement in diseasei
Cerebellar ataxia, non-progressive, with mental retardation (CANPMR)1 Publication
The disease is caused by mutations affecting the gene represented in this entry.
Disease descriptionA neurodevelopmental disorder characterized by mildly delayed psychomotor development, early onset of cerebellar ataxia, and intellectual disability later in childhood and adult life. Other features may include neonatal hypotonia, dysarthria, and dysmetria. Brain imaging in some patients shows cerebellar atrophy. Dysmorphic facial features are variable.
Related information in OMIMKeywords - Diseasei
Mental retardationOrganism-specific databases
DisGeNETi | 23261 |
MalaCardsi | CAMTA1 |
MIMi | 614756 phenotype |
OpenTargetsi | ENSG00000171735 |
Orphaneti | 157791 Epithelioid hemangioendothelioma 314647 Non-progressive cerebellar ataxia with intellectual disability |
PharmGKBi | PA38688 |
Miscellaneous databases
Pharosi | Q9Y6Y1 |
Polymorphism and mutation databases
BioMutai | CAMTA1 |
DMDMi | 97046872 |
PTM / Processingi
Molecule processing
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
ChainiPRO_0000235820 | 1 – 1673 | Calmodulin-binding transcription activator 1Add BLAST | 1673 |
Proteomic databases
jPOSTi | Q9Y6Y1 |
MassIVEi | Q9Y6Y1 |
PaxDbi | Q9Y6Y1 |
PeptideAtlasi | Q9Y6Y1 |
PRIDEi | Q9Y6Y1 |
ProteomicsDBi | 33093 86825 [Q9Y6Y1-1] 86826 [Q9Y6Y1-2] 86827 [Q9Y6Y1-3] |
PTM databases
iPTMneti | Q9Y6Y1 |
PhosphoSitePlusi | Q9Y6Y1 |
Expressioni
Tissue specificityi
Normally expressed in non-neoplastic adult central nervous system tissues: detected in whole brain, cerebellum, brain cortex, occipital lobe, frontal lobe, temporal lobe, putamen. Expression levels are low in oligodendroglial tumors, and are reduced by half in oligodendroglioma and astrocytoma cases with 1p loss of heterozygosity. Detected in neuroblastic-type cultured neuroblastoma cells. Expressed in heart and kidney.3 Publications
Inductioni
Detected at low levels at interphase and in resting cells. Up-regulated during S phase and mitosis. Levels decrease at the end of mitosis.1 Publication
Gene expression databases
Bgeei | ENSG00000171735 Expressed in 218 organ(s), highest expression level in caudate nucleus |
ExpressionAtlasi | Q9Y6Y1 baseline and differential |
Genevisiblei | Q9Y6Y1 HS |
Organism-specific databases
HPAi | HPA036342 HPA036343 |
Interactioni
Subunit structurei
May interact with calmodulin.
CuratedProtein-protein interaction databases
BioGridi | 116863, 4 interactors |
IntActi | Q9Y6Y1, 1 interactor |
STRINGi | 9606.ENSP00000306522 |
Structurei
Secondary structure
Legend: HelixTurnBeta strandPDB Structure known for this area
Show more details3D structure databases
SMRi | Q9Y6Y1 |
ModBasei | Search... |
PDBe-KBi | Search... |
Miscellaneous databases
EvolutionaryTracei | Q9Y6Y1 |
Family & Domainsi
Domains and Repeats
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Domaini | 873 – 953 | IPT/TIGAdd BLAST | 81 | |
Repeati | 1064 – 1093 | ANK 1Add BLAST | 30 | |
Repeati | 1109 – 1129 | ANK 2Add BLAST | 21 | |
Repeati | 1143 – 1172 | ANK 3Add BLAST | 30 | |
Domaini | 1547 – 1576 | IQ 1PROSITE-ProRule annotationAdd BLAST | 30 | |
Domaini | 1577 – 1599 | IQ 2PROSITE-ProRule annotationAdd BLAST | 23 | |
Domaini | 1600 – 1622 | IQ 3PROSITE-ProRule annotationAdd BLAST | 23 |
Motif
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Motifi | 112 – 119 | Nuclear localization signalPROSITE-ProRule annotation | 8 |
Compositional bias
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Compositional biasi | 499 – 502 | Poly-Gly | 4 | |
Compositional biasi | 1038 – 1041 | Poly-Val | 4 |
Sequence similaritiesi
Belongs to the CAMTA family.Curated
Keywords - Domaini
ANK repeat, RepeatPhylogenomic databases
eggNOGi | KOG0520 Eukaryota ENOG410XS5M LUCA |
GeneTreei | ENSGT00940000155203 |
HOGENOMi | HOG000111813 |
InParanoidi | Q9Y6Y1 |
KOi | K21596 |
OMAi | GKNEHSH |
OrthoDBi | 315169at2759 |
PhylomeDBi | Q9Y6Y1 |
TreeFami | TF323452 |
Family and domain databases
Gene3Di | 1.25.40.20, 1 hit 2.60.40.10, 1 hit |
InterProi | View protein in InterPro IPR002110 Ankyrin_rpt IPR020683 Ankyrin_rpt-contain_dom IPR036770 Ankyrin_rpt-contain_sf IPR039033 Camta1 IPR005559 CG-1_dom IPR013783 Ig-like_fold IPR014756 Ig_E-set IPR002909 IPT_dom IPR000048 IQ_motif_EF-hand-BS IPR027417 P-loop_NTPase |
PANTHERi | PTHR23335:SF11 PTHR23335:SF11, 1 hit |
Pfami | View protein in Pfam PF03859 CG-1, 1 hit PF00612 IQ, 1 hit PF01833 TIG, 1 hit |
SMARTi | View protein in SMART SM01076 CG-1, 1 hit |
SUPFAMi | SSF48403 SSF48403, 1 hit SSF52540 SSF52540, 1 hit SSF81296 SSF81296, 1 hit |
PROSITEi | View protein in PROSITE PS50297 ANK_REP_REGION, 1 hit PS50088 ANK_REPEAT, 1 hit PS51437 CG_1, 1 hit PS50096 IQ, 1 hit |
s (4+)i Sequence
Sequence statusi: Complete.
This entry describes 4 produced by isoformsialternative splicing. AlignAdd to basketThis entry has 4 described isoforms and 7 potential isoforms that are computationally mapped.Show allAlign All
Isoform 1 (identifier: Q9Y6Y1-1) [UniParc]FASTAAdd to basket
This isoform has been chosen as the sequence. All positional information in this entry refers to it. This is also the sequence that appears in the downloadable versions of the entry. canonicali
10 20 30 40 50
MWRAEGKWLP KTSRKSVSQS VFCGTSTYCV LNTVPPIEDD HGNSNSSHVK
60 70 80 90 100
IFLPKKLLEC LPKCSSLPKE RHRWNTNEEI AAYLITFEKH EEWLTTSPKT
110 120 130 140 150
RPQNGSMILY NRKKVKYRKD GYCWKKRKDG KTTREDHMKL KVQGVECLYG
160 170 180 190 200
CYVHSSIIPT FHRRCYWLLQ NPDIVLVHYL NVPAIEDCGK PCGPILCSIN
210 220 230 240 250
TDKKEWAKWT KEELIGQLKP MFHGIKWTCS NGNSSSGFSV EQLVQQILDS
260 270 280 290 300
HQTKPQPRTH NCLCTGSLGA GGSVHHKCNS AKHRIISPKV EPRTGGYGSH
310 320 330 340 350
SEVQHNDVSE GKHEHSHSKG SSREKRNGKV AKPVLLHQSS TEVSSTNQVE
360 370 380 390 400
VPDTTQSSPV SISSGLNSDP DMVDSPVVTG VSGMAVASVM GSLSQSATVF
410 420 430 440 450
MSEVTNEAVY TMSPTAGPNH HLLSPDASQG LVLAVSSDGH KFAFPTTGSS
460 470 480 490 500
ESLSMLPTNV SEELVLSTTL DGGRKIPETT MNFDPDCFLN NPKQGQTYGG
510 520 530 540 550
GGLKAEMVSS NIRHSPPGER SFSFTTVLTK EIKTEDTSFE QQMAKEAYSS
560 570 580 590 600
SAAAVAASSL TLTAGSSLLP SGGGLSPSTT LEQMDFSAID SNKDYTSSFS
610 620 630 640 650
QTGHSPHIHQ TPSPSFFLQD ASKPLPVEQN THSSLSDSGG TFVMPTVKTE
660 670 680 690 700
ASSQTSSCSG HVETRIESTS SLHLMQFQAN FQAMTAEGEV TMETSQAAEG
710 720 730 740 750
SEVLLKSGEL QACSSEHYLQ PETNGVIRSA GGVPILPGNV VQGLYPVAQP
760 770 780 790 800
SLGNASNMEL SLDHFDISFS NQFSDLINDF ISVEGGSSTI YGHQLVSGDS
810 820 830 840 850
TALSQSEDGA RAPFTQAEMC LPCCSPQQGS LQLSSSEGGA STMAYMHVAE
860 870 880 890 900
VVSAASAQGT LGMLQQSGRV FMVTDYSPEW SYPEGGVKVL ITGPWQEASN
910 920 930 940 950
NYSCLFDQIS VPASLIQPGV LRCYCPAHDT GLVTLQVAFN NQIISNSVVF
960 970 980 990 1000
EYKARALPTL PSSQHDWLSL DDNQFRMSIL ERLEQMERRM AEMTGSQQHK
1010 1020 1030 1040 1050
QASGGGSSGG GSGSGNGGSQ AQCASGTGAL GSCFESRVVV VCEKMMSRAC
1060 1070 1080 1090 1100
WAKSKHLIHS KTFRGMTLLH LAAAQGYATL IQTLIKWRTK HADSIDLELE
1110 1120 1130 1140 1150
VDPLNVDHFS CTPLMWACAL GHLEAAVVLY KWDRRAISIP DSLGRLPLGI
1160 1170 1180 1190 1200
ARSRGHVKLA ECLEHLQRDE QAQLGQNPRI HCPASEEPST ESWMAQWHSE
1210 1220 1230 1240 1250
AISSPEIPKG VTVIASTNPE LRRPRSEPSN YYSSESHKDY PAPKKHKLNP
1260 1270 1280 1290 1300
EYFQTRQEKL LPTALSLEEP NIRKQSPSSK QSVPETLSPS EGVRDFSREL
1310 1320 1330 1340 1350
SPPTPETAAF QASGSQPVGK WNSKDLYIGV STVQVTGNPK GTSVGKEAAP
1360 1370 1380 1390 1400
SQVRPREPMS VLMMANREVV NTELGSYRDS AENEECGQPM DDIQVNMMTL
1410 1420 1430 1440 1450
AEHIIEATPD RIKQENFVPM ESSGLERTDP ATISSTMSWL ASYLADADCL
1460 1470 1480 1490 1500
PSAAQIRSAY NEPLTPSSNT SLSPVGSPVS EIAFEKPNLP SAADWSEFLS
1510 1520 1530 1540 1550
ASTSEKVENE FAQLTLSDHE QRELYEAARL VQTAFRKYKG RPLREQQEVA
1560 1570 1580 1590 1600
AAVIQRCYRK YKQYALYKKM TQAAILIQSK FRSYYEQKKF QQSRRAAVLI
1610 1620 1630 1640 1650
QKYYRSYKKC GKRRQARRTA VIVQQKLRSS LLTKKQDQAA RKIMRFLRRC
1660 1670
RHSPLVDHRL YKRSERIEKG QGT
Computationally mapped potential isoform sequencesi
There are 7 potential isoforms mapped to this entry.BLASTAlignShow allAdd to basketH0YJK7 | H0YJK7_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 637 | Annotation score: | ||
H0YJR7 | H0YJR7_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 239 | Annotation score: | ||
A0A0C4DGL0 | A0A0C4DGL0_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 237 | Annotation score: | ||
H0YJG5 | H0YJG5_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 39 | Annotation score: | ||
H0YJV1 | H0YJV1_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 73 | Annotation score: | ||
G3V297 | G3V297_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 92 | Annotation score: | ||
H0YJY7 | H0YJY7_HUMAN | Calmodulin-binding transcription ac... | CAMTA1 | 44 | Annotation score: |
Sequence cautioni
The sequence AAL39006 differs from that shown. Reason: Erroneous initiation. Truncated N-terminus.Curated
The sequence BAA74856 differs from that shown. Reason: Erroneous initiation. Extended N-terminus.Curated
The sequence EAW71580 differs from that shown. Reason: Erroneous gene model prediction.Curated
Natural variant
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Natural variantiVAR_047824 | 1177 | N → K1 PublicationCorresponds to variant dbSNP:rs41278952EnsemblClinVar. | 1 | |
Natural variantiVAR_047825 | 1218 | N → T1 PublicationCorresponds to variant dbSNP:rs41278954Ensembl. | 1 | |
Natural variantiVAR_047826 | 1336 | T → I1 PublicationCorresponds to variant dbSNP:rs137974312Ensembl. | 1 |
Alternative sequence
Feature key | Position(s) | DescriptionActions | Graphical view | Length |
---|---|---|---|---|
Alternative sequenceiVSP_046358 | 79 – 101 | EIAAY…SPKTR → ALTTHLFMGAAKKRDPQSWS HEG in isoform 4. 1 PublicationAdd BLAST | 23 | |
Alternative sequenceiVSP_043842 | 79 – 80 | EI → RS in isoform 3. 2 Publications | 2 | |
Alternative sequenceiVSP_043843 | 81 – 1673 | Missing in isoform 3. 2 PublicationsAdd BLAST | 1593 | |
Alternative sequenceiVSP_046359 | 102 – 1673 | Missing in isoform 4. 1 PublicationAdd BLAST | 1572 | |
Alternative sequenceiVSP_035936 | 1458 – 1471 | Missing in isoform 2. 2 PublicationsAdd BLAST | 14 | |
Alternative sequenceiVSP_035937 | 1653 – 1673 | SPLVD…KGQGT → RVKELKKAKELEDIQQHPLA M in isoform 2. 2 PublicationsAdd BLAST | 21 |
Sequence databases
Select the link destinations: EMBLi GenBanki DDBJi Links Updated | AB020640 mRNA Translation: BAA74856.3 Different initiation. AY037153 mRNA Translation: AAK67633.1 AL359881 Genomic DNA No translation available. AL365194 Genomic DNA No translation available. AL590128 Genomic DNA No translation available. AL596210 Genomic DNA No translation available. Z97635 Genomic DNA No translation available. Z98052 Genomic DNA No translation available. Z98884 Genomic DNA No translation available. CH471130 Genomic DNA Translation: EAW71580.1 Sequence problems. BC116457 mRNA Translation: AAI16458.1 BC151835 mRNA Translation: AAI51836.1 CD103791 mRNA No translation available. AF111804 mRNA Translation: AAL39006.1 Different initiation. AY349360 mRNA Translation: AAQ56724.1 |
CCDSi | CCDS30576.1 [Q9Y6Y1-1] CCDS55574.1 [Q9Y6Y1-3] CCDS55575.1 [Q9Y6Y1-4] |
RefSeqi | NP_001182492.1, NM_001195563.1 [Q9Y6Y1-3] NP_001229630.1, NM_001242701.1 [Q9Y6Y1-4] NP_056030.1, NM_015215.3 [Q9Y6Y1-1] |
Genome annotation databases
Ensembli | ENST00000303635; ENSP00000306522; ENSG00000171735 [Q9Y6Y1-1] ENST00000473578; ENSP00000451388; ENSG00000171735 [Q9Y6Y1-3] ENST00000557126; ENSP00000451510; ENSG00000171735 [Q9Y6Y1-4] |
GeneIDi | 23261 |
KEGGi | hsa:23261 |
UCSCi | uc001aoh.4 human [Q9Y6Y1-1] |
Keywords - Coding sequence diversityi
Alternative splicing, PolymorphismSimilar proteinsi
Cross-referencesi
Web resourcesi
Atlas of Genetics and Cytogenetics in Oncology and Haematology |
Sequence databases
Select the link destinations: EMBLi GenBanki DDBJi Links Updated | AB020640 mRNA Translation: BAA74856.3 Different initiation. AY037153 mRNA Translation: AAK67633.1 AL359881 Genomic DNA No translation available. AL365194 Genomic DNA No translation available. AL590128 Genomic DNA No translation available. AL596210 Genomic DNA No translation available. Z97635 Genomic DNA No translation available. Z98052 Genomic DNA No translation available. Z98884 Genomic DNA No translation available. CH471130 Genomic DNA Translation: EAW71580.1 Sequence problems. BC116457 mRNA Translation: AAI16458.1 BC151835 mRNA Translation: AAI51836.1 CD103791 mRNA No translation available. AF111804 mRNA Translation: AAL39006.1 Different initiation. AY349360 mRNA Translation: AAQ56724.1 |
CCDSi | CCDS30576.1 [Q9Y6Y1-1] CCDS55574.1 [Q9Y6Y1-3] CCDS55575.1 [Q9Y6Y1-4] |
RefSeqi | NP_001182492.1, NM_001195563.1 [Q9Y6Y1-3] NP_001229630.1, NM_001242701.1 [Q9Y6Y1-4] NP_056030.1, NM_015215.3 [Q9Y6Y1-1] |
3D structure databases
Select the link destinations: PDBei RCSB PDBi PDBji Links Updated | PDB entry | Method | Resolution (Å) | Chain | Positions | PDBsum |
2CXK | X-ray | 1.85 | A/B/C/D/E | 872-953 | [»] | |
SMRi | Q9Y6Y1 | |||||
ModBasei | Search... | |||||
PDBe-KBi | Search... |
Protein-protein interaction databases
BioGridi | 116863, 4 interactors |
IntActi | Q9Y6Y1, 1 interactor |
STRINGi | 9606.ENSP00000306522 |
PTM databases
iPTMneti | Q9Y6Y1 |
PhosphoSitePlusi | Q9Y6Y1 |
Polymorphism and mutation databases
BioMutai | CAMTA1 |
DMDMi | 97046872 |
Proteomic databases
jPOSTi | Q9Y6Y1 |
MassIVEi | Q9Y6Y1 |
PaxDbi | Q9Y6Y1 |
PeptideAtlasi | Q9Y6Y1 |
PRIDEi | Q9Y6Y1 |
ProteomicsDBi | 33093 86825 [Q9Y6Y1-1] 86826 [Q9Y6Y1-2] 86827 [Q9Y6Y1-3] |
Genome annotation databases
Ensembli | ENST00000303635; ENSP00000306522; ENSG00000171735 [Q9Y6Y1-1] ENST00000473578; ENSP00000451388; ENSG00000171735 [Q9Y6Y1-3] ENST00000557126; ENSP00000451510; ENSG00000171735 [Q9Y6Y1-4] |
GeneIDi | 23261 |
KEGGi | hsa:23261 |
UCSCi | uc001aoh.4 human [Q9Y6Y1-1] |
Organism-specific databases
CTDi | 23261 |
DisGeNETi | 23261 |
GeneCardsi | CAMTA1 |
HGNCi | HGNC:18806 CAMTA1 |
HPAi | HPA036342 HPA036343 |
MalaCardsi | CAMTA1 |
MIMi | 611501 gene 614756 phenotype |
neXtProti | NX_Q9Y6Y1 |
OpenTargetsi | ENSG00000171735 |
Orphaneti | 157791 Epithelioid hemangioendothelioma 314647 Non-progressive cerebellar ataxia with intellectual disability |
PharmGKBi | PA38688 |
HUGEi | Search... |
GenAtlasi | Search... |
Phylogenomic databases
eggNOGi | KOG0520 Eukaryota ENOG410XS5M LUCA |
GeneTreei | ENSGT00940000155203 |
HOGENOMi | HOG000111813 |
InParanoidi | Q9Y6Y1 |
KOi | K21596 |
OMAi | GKNEHSH |
OrthoDBi | 315169at2759 |
PhylomeDBi | Q9Y6Y1 |
TreeFami | TF323452 |
Enzyme and pathway databases
SIGNORi | Q9Y6Y1 |
Miscellaneous databases
ChiTaRSi | CAMTA1 human |
EvolutionaryTracei | Q9Y6Y1 |
GeneWikii | CAMTA1 |
GenomeRNAii | 23261 |
Pharosi | Q9Y6Y1 |
PROi | PR:Q9Y6Y1 |
SOURCEi | Search... |
Gene expression databases
Bgeei | ENSG00000171735 Expressed in 218 organ(s), highest expression level in caudate nucleus |
ExpressionAtlasi | Q9Y6Y1 baseline and differential |
Genevisiblei | Q9Y6Y1 HS |
Family and domain databases
Gene3Di | 1.25.40.20, 1 hit 2.60.40.10, 1 hit |
InterProi | View protein in InterPro IPR002110 Ankyrin_rpt IPR020683 Ankyrin_rpt-contain_dom IPR036770 Ankyrin_rpt-contain_sf IPR039033 Camta1 IPR005559 CG-1_dom IPR013783 Ig-like_fold IPR014756 Ig_E-set IPR002909 IPT_dom IPR000048 IQ_motif_EF-hand-BS IPR027417 P-loop_NTPase |
PANTHERi | PTHR23335:SF11 PTHR23335:SF11, 1 hit |
Pfami | View protein in Pfam PF03859 CG-1, 1 hit PF00612 IQ, 1 hit PF01833 TIG, 1 hit |
SMARTi | View protein in SMART SM01076 CG-1, 1 hit |
SUPFAMi | SSF48403 SSF48403, 1 hit SSF52540 SSF52540, 1 hit SSF81296 SSF81296, 1 hit |
PROSITEi | View protein in PROSITE PS50297 ANK_REP_REGION, 1 hit PS50088 ANK_REPEAT, 1 hit PS51437 CG_1, 1 hit PS50096 IQ, 1 hit |
ProtoNeti | Search... |
MobiDBi | Search... |
Entry informationi
Entry namei | CMTA1_HUMAN | |
Accessioni | Q9Y6Y1Primary (citable) accession number: Q9Y6Y1 Secondary accession number(s): A7MBM4 Q96S92 | |
Entry historyi | Integrated into UniProtKB/Swiss-Prot: | May 16, 2006 |
Last sequence update: | May 16, 2006 | |
Last modified: | October 16, 2019 | |
This is version 158 of the entry and version 4 of the sequence. See complete history. | ||
Entry statusi | Reviewed (UniProtKB/Swiss-Prot) | |
Annotation program | Chordata Protein Annotation Program | |
Disclaimer | Any 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. |
Miscellaneousi
Keywords - Technical termi
3D-structure, Complete proteome, Reference proteomeDocuments
- Human chromosome 1
Human chromosome 1: entries, gene names and cross-references to MIM - Human entries with polymorphisms or disease mutations
List of human entries with polymorphisms or disease mutations - SIMILARITY comments
Index of protein domains and families - Human polymorphisms and disease mutations
Index of human polymorphisms and disease mutations - MIM cross-references
Online Mendelian Inheritance in Man (MIM) cross-references in UniProtKB/Swiss-Prot - PDB cross-references
Index of Protein Data Bank (PDB) cross-references