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Gene Gene information from NCBI Gene database.
Entrez ID 338094
Gene name Family with sequence similarity 151 member A
Gene symbol FAM151A
Synonyms (NCBI Gene)
C1orf179
Chromosome 1
Chromosome location -
miRNA miRNA information provided by mirtarbase database.
4
miRTarBase ID miRNA Experiments Reference
MIRT017107 hsa-miR-335-5p Microarray 18185580
MIRT980848 hsa-miR-3136-3p CLIP-seq
MIRT980849 hsa-miR-331-3p CLIP-seq
MIRT980850 hsa-miR-4292 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
6 Show/Hide all (6)
GO ID Ontology Definition Evidence Reference
GO:0003674 Function Molecular_function ND
GO:0005615 Component Extracellular space IBA
GO:0008150 Process Biological_process ND
GO:0016020 Component Membrane IEA
GO:0016020 Component Membrane NAS 12975309
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.
Q8WW52
Protein name Protein FAM151A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10223 DUF2181 66 → 306 Uncharacterized conserved protein (DUF2181) Family
PF10223 DUF2181 338 → 575 Uncharacterized conserved protein (DUF2181) Family
Sequence
Sequence length 585
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
7
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.
Show/Hide Unknown Diseases (7)
Phenotype Name Clinical Significance Source Reference Evidence Score
Clear cell carcinoma of kidney Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Colon adenocarcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Familial cancer of breast Likely benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Hepatocellular carcinoma Benign ClinVar —
★★★★★
★★☆☆☆
Found in Text Mining + Unknown/Other Associations