Gene Gene information from NCBI Gene database.
Entrez ID 84923
Gene name VCP nuclear cofactor family member 1
Gene symbol VCF1
Synonyms (NCBI Gene)
FAM104A
Chromosome 17
Chromosome location 17q25.1
miRNA miRNA information provided by mirtarbase database.
513
miRTarBase ID miRNA Experiments Reference
MIRT025019 hsa-miR-183-5p Sequencing 20371350
MIRT025497 hsa-miR-34a-5p Sequencing 20371350
MIRT026086 hsa-miR-196a-5p Sequencing 20371350
MIRT032171 hsa-let-7d-5p Sequencing 20371350
MIRT050694 hsa-miR-18a-5p CLASH 23622248
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 25416956, 32296183, 32814053, 33961781
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
621109 25918 ENSG00000133193
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q969W3
Protein name Protein VCF1 (VCP nuclear cofactor family member 1)
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15434 FAM104 74 186 Family 104 Family
Sequence
Sequence length 186
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 Evidence Score
CONGENITAL DISORDER OF GLYCOSYLATION, TYPE 2G Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations