Gene Gene information from NCBI Gene database.
Entrez ID 404550
Gene name Chromosome 16 open reading frame 74
Gene symbol C16orf74
Synonyms (NCBI Gene)
ASRACLMBMICT1
Chromosome 16
Chromosome location 16q24.1
miRNA miRNA information provided by mirtarbase database.
101
miRTarBase ID miRNA Experiments Reference
MIRT503240 hsa-miR-6165 PAR-CLIP 20371350
MIRT503239 hsa-miR-6858-3p PAR-CLIP 20371350
MIRT503238 hsa-miR-4722-5p PAR-CLIP 20371350
MIRT503237 hsa-miR-3194-5p PAR-CLIP 20371350
MIRT503236 hsa-miR-505-5p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
1
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 16189514, 25416956, 28881575, 32296183
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.
Q96GX8
Protein name Uncharacterized protein C16orf74
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15366 DUF4597 13 75 Domain of unknown function (DUF4597) Family
Tissue specificity TISSUE SPECIFICITY: [Isoform 1]: Not expressed in pancreatic duct cells (at protein level). Abundantly expressed in the pancreas and weakly expressed in the thyroid. {ECO:0000269|PubMed:28881575}.; TISSUE SPECIFICITY: [Isoform 2]: Not expressed in pancrea
Sequence
Sequence length 76
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
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
COLOR VISION 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
ANOPHTHALMIA AND PULMONARY HYPOPLASIA Syndromic microphthalmia BEFREE 29371937, 31597713
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus, Non-Insulin-Dependent Diabetes Mellitus GWASCAT_DG 26818947
★☆☆☆☆
Found in Text Mining only
Malignant neoplasm of pancreas Pancreatic cancer BEFREE 31597713
★☆☆☆☆
Found in Text Mining only
Neoplasms Neoplasms BEFREE 21203532, 29371937
★☆☆☆☆
Found in Text Mining only
Pancreatic carcinoma Pancreatic carcinoma BEFREE 31597713
★☆☆☆☆
Found in Text Mining only
Prostatic Neoplasms Prostatic neoplasm Pubtator 35234293 Associate
★☆☆☆☆
Found in Text Mining only
Urinary Bladder Neoplasms Urinary bladder neoplasms Pubtator 21203532 Associate
★☆☆☆☆
Found in Text Mining only