Gene Gene information from NCBI Gene database.
Entrez ID 132720
Gene name Family with sequence similarity 241 member A
Gene symbol FAM241A
Synonyms (NCBI Gene)
C4orf32
Chromosome 4
Chromosome location 4q25
miRNA miRNA information provided by mirtarbase database.
163
miRTarBase ID miRNA Experiments Reference
MIRT530522 hsa-miR-3120-3p HITS-CLIP 23313552
MIRT530521 hsa-miR-181c-3p HITS-CLIP 23313552
MIRT530520 hsa-miR-5586-3p HITS-CLIP 23313552
MIRT530519 hsa-miR-548p HITS-CLIP 23313552
MIRT530518 hsa-miR-759 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:0005515 Function Protein binding IPI 33961781
GO:0005794 Component Golgi apparatus IDA
GO:0016020 Component Membrane IEA
GO:0043231 Component Intracellular membrane-bounded organelle IBA
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.
Q8N8J7
Protein name Uncharacterized protein FAM241A
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15378 DUF4605 73 131 Domain of unknown function (DUF4605) Family
Sequence
MCSAGELLRGGDGGERDEDGDALAEREAAGTGWDPGASPRRRGQRPKESEQDVEDSQNHT
GEPVGDDYKKMGTLFGELNKNLINMGFTRMYFGERIVEPVIVIFFWVMLWFLGLQALGLV
AVLCLVIIYVQ
Q
Sequence length 132
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
DISORDER OF PHARYNX GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
MULTIPLE SCLEROSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TESTICULAR HYDROCELE GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations