Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
84660
Gene name Gene Name - the full gene name approved by the HGNC.
Coiled-coil domain containing 62
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
CCDC62
Synonyms (NCBI Gene) Gene synonyms aliases
CT109, ERAP75, SPGF67, TSP-NY
Chromosome Chromosome number
12
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
12q24.31
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT724653 hsa-miR-4714-5p HITS-CLIP 19536157
MIRT724652 hsa-miR-345-5p HITS-CLIP 19536157
MIRT724651 hsa-miR-4522 HITS-CLIP 19536157
MIRT724650 hsa-miR-3161 HITS-CLIP 19536157
MIRT724653 hsa-miR-4714-5p HITS-CLIP 19536157
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0001669 Component Acrosomal vesicle IDA 28339613
GO:0001669 Component Acrosomal vesicle IEA
GO:0001835 Process Blastocyst hatching IEA
GO:0003713 Function Transcription coactivator activity IPI 18563714, 19126643
GO:0005515 Function Protein binding IPI 19126643
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
613481 30723 ENSG00000130783
Protein
UniProt ID Q6P9F0
Protein name Coiled-coil domain-containing protein 62 (Protein TSP-NY) (Protein aaa)
Protein function Nuclear receptor coactivator that can enhance preferentially estrogen receptors ESR1 and ESR2 transactivation. Also modulates progesterone/PGR, glucocorticoid/NR3C1 and androgen/AR receptors transactivation, although at lower level; little effec
Family and domains
Tissue specificity TISSUE SPECIFICITY: Highly expressed in adult testis. Expressed in both prostate epithelial and stromal cells, with predominant expression in epithelial cells (at protein level) (PubMed:19126643). Not detected in prostate by RT-PCR (PubMed:19165854). Over
Sequence
MNPPAAFLAGRQNIGSEVEISTIEKQRKELQLLIGELKDRDKELNDMVAVHQQQLLSWEE
DRQKVLTLEERCSKLEGELHKRTEIIRSLTKKVKALESNQMECQTALQKTQLQLQEMAQK
ATHSSLLSEDLEARNETLSNTLVELSAQVGQLQAREQALTTMIKLKDKDIIEAVNHIADC
SGKFKMLEHALRDAKMAETCIVKEKQDYKQKLKALKIEVNKLKEDLNEKTTENNEQREEI
IRLKQEKSCLHDELLFTVEREKRKDELLNIAKSKQERTNSELHNLRQIYVKQQSDLQFLN
FNVENSQELIQMYDSKMEESKALDSSRDMCLSDLENNHPKVDIKREKNQKSLFKDQKFEA
MLVQQNRSDKSSCDECKEKKQQIDTVFGEKSVITLSSIFTKDLVEKHNLPWSLGGKTQIE
PENKITLCKIHTKSPKCHGTGVQNEGKQPSETPTLSDEKQWHDVSVYLGLTNCPSSKHPE
KLDVECQDQMERSEISCCQKNEACLGESGMCDSKCCHPSNFIIEAPGHMSDVEWMSIFKP
SKMQRIVRLKSGCTCSESICGTQHDSPASELIAIQDSHSLGSSKSALREDETESSSNKKN
SPTSLLIYKDAPAFNEKASIVLPSQDDFSPTSKLQRLLAESRQMVTDLELSTLLPISHEN
LTGSATNKSEVPEESAQKNTFVSY
Sequence length 684
Interactions View interactions
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Associated diseases Disease associations categorized as Causal (pathogenic variants), Unknown (uncertain genetic evidence), or Text Mining (literature-based associations)
Unknown Includes: (1) ClinVar NON-pathogenic variants (Uncertain, Benign, Conflicting, VUS), (2) GenCC associations, (3) GWAS associations, (4) CBGDA evidence-based associations. NOTE: Diseases with pathogenic evidence are excluded to avoid conflicts.
Disease merge term Disease name Evidence References Source
Atrial Fibrillation Atrial fibrillation N/A N/A GWAS
Insomnia Insomnia N/A N/A GWAS
Parkinson Disease Parkinson's disease N/A N/A GWAS
Schizophrenia Schizophrenia N/A N/A GWAS
Associations from Text Mining Disease associations identified through Pubtator
Disease Name Relationship Type References
Autonomic Nervous System Diseases Associate 34994165
Hypokinesia Associate 24514572
Inflammation Associate 36926335
Parkinson Disease Associate 21812969, 24514572, 34994165, 36926335
Parkinson Disease Stimulate 24312176
Parkinson Disease Secondary Associate 24514572
Teratozoospermia Associate 31985809