Gene Gene information from NCBI Gene database.
Entrez ID 285382
Gene name Chromosome 3 open reading frame 70
Gene symbol C3orf70
Synonyms (NCBI Gene)
-
Chromosome 3
Chromosome location 3q27.2
miRNA miRNA information provided by mirtarbase database.
334
miRTarBase ID miRNA Experiments Reference
MIRT688890 hsa-miR-508-5p HITS-CLIP 23313552
MIRT688889 hsa-miR-6849-3p HITS-CLIP 23313552
MIRT688888 hsa-miR-6742-3p HITS-CLIP 23313552
MIRT688887 hsa-miR-766-3p HITS-CLIP 23313552
MIRT688886 hsa-miR-4793-3p 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:0007399 Process Nervous system development IBA
GO:0007399 Process Nervous system development IEA
GO:0007399 Process Nervous system development ISS
GO:0048512 Process Circadian behavior ISS
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.
A6NLC5
Protein name UPF0524 protein C3orf70
Protein function May play a role in neuronal and neurobehavioral development.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15823 UPF0524 14 250 UPF0524 of C3orf70 Family
Sequence
Sequence length 250
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
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Obesity Obesity Pubtator 29084944 Associate
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Urinary bladder neoplasms Pubtator 31077629, 33204364 Associate
★☆☆☆☆
Found in Text Mining only