Gene Gene information from NCBI Gene database.
Entrez ID 9715
Gene name Family with sequence similarity 131 member B
Gene symbol FAM131B
Synonyms (NCBI Gene)
-
Chromosome 7
Chromosome location 7q34
miRNA miRNA information provided by mirtarbase database.
123
miRTarBase ID miRNA Experiments Reference
MIRT716308 hsa-miR-3614-3p HITS-CLIP 19536157
MIRT716307 hsa-miR-4530 HITS-CLIP 19536157
MIRT716306 hsa-miR-338-3p HITS-CLIP 19536157
MIRT716305 hsa-miR-766-3p HITS-CLIP 19536157
MIRT716304 hsa-miR-3925-3p HITS-CLIP 19536157
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 21044950
GO:0005654 Component Nucleoplasm IDA
GO:0005829 Component Cytosol IDA
GO:0005829 Component Cytosol TAS
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
619282 22202 ENSG00000159784
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q86XD5
Protein name Protein FAM131B
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF15010 FAM131 33 325 Putative cell signalling Family
Sequence
Sequence length 332
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    Signaling by BRAF and RAF fusions
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
BECKER GENERALIZED MYOTONIA Disgenet
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
EBV-positive nodal T- and NK-cell lymphoma Likely benign ClinVar
★★☆☆☆
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
Astrocytoma Astrocytoma Pubtator 25040262 Associate
★☆☆☆☆
Found in Text Mining only
Brain Neoplasms Brain Neoplasms BEFREE 28597942
★☆☆☆☆
Found in Text Mining only
Dysembryoplastic neuroepithelial tumor Dysembryoplastic Neuroepithelial Tumor BEFREE 24767714, 25040262
★☆☆☆☆
Found in Text Mining only
Glioma Glioma Pubtator 25040262 Associate
★☆☆☆☆
Found in Text Mining only
Pilocytic Astrocytoma Astrocytoma BEFREE 21424530, 25040262
★☆☆☆☆
Found in Text Mining only