Gene Gene information from NCBI Gene database.
Entrez ID 375341
Gene name Chromosome 3 open reading frame 62
Gene symbol C3orf62
Synonyms (NCBI Gene)
MAPS
Chromosome 3
Chromosome location 3p21.31
miRNA miRNA information provided by mirtarbase database.
370
miRTarBase ID miRNA Experiments Reference
MIRT693893 hsa-miR-6499-3p HITS-CLIP 23313552
MIRT693892 hsa-miR-3135b HITS-CLIP 23313552
MIRT693891 hsa-miR-504-3p HITS-CLIP 23313552
MIRT693890 hsa-miR-122-5p HITS-CLIP 23313552
MIRT693889 hsa-miR-3652 HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
4
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956, 31515488, 32296183, 32814053
GO:0007283 Process Spermatogenesis IEA
GO:0007283 Process Spermatogenesis ISS
GO:0030154 Process Cell differentiation IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q6ZUJ4
Protein name Uncharacterized protein C3orf62
Protein function Essential for normal spermatogenesis and male fertility.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15830 DUF4712 13 266 Domain of unknown function (DUF4712) Family
Tissue specificity TISSUE SPECIFICITY: Testis. Down-regulated in men with spermatocyte arrest. {ECO:0000269|PubMed:31930642}.
Sequence
Sequence length 267
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
3
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
INSOMNIA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MAJOR DEPRESSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
NEUROTIC DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Neoplasms Associate 37965307
★☆☆☆☆
Found in Text Mining only
Soft Tissue Neoplasms Associate 28248815
★☆☆☆☆
Found in Text Mining only