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Gene Gene information from NCBI Gene database.
Entrez ID 339448
Gene name Chromosome 1 open reading frame 174
Gene symbol C1orf174
Synonyms (NCBI Gene)
-
Chromosome 1
Chromosome location 1p36.32
miRNA miRNA information provided by mirtarbase database.
321 Show/Hide all (321)
miRTarBase ID miRNA Experiments Reference
MIRT048934 hsa-miR-92a-3p CLASH 23622248
MIRT047184 hsa-miR-182-5p CLASH 23622248
MIRT040494 hsa-miR-598-3p CLASH 23622248
MIRT684531 hsa-miR-34b-3p HITS-CLIP 23313552
MIRT684530 hsa-miR-4695-5p HITS-CLIP 23313552
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
3
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 21044950, 25416956, 28514442, 31515488, 32296183, 32707033, 33961781
GO:0005634 Component Nucleus IEA
GO:0005654 Component Nucleoplasm IDA
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.
Q8IYL3
Protein name UPF0688 protein C1orf174
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15772 UPF0688 6 → 237 UPF0688 family Family
Sequence
Sequence length 243
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
1
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 Reference Evidence Score
Familial cancer of breast Uncertain significance ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations