Gene Gene information from NCBI Gene database.
Entrez ID 283742
Gene name Family with sequence similarity 98 member B
Gene symbol FAM98B
Synonyms (NCBI Gene)
-
Chromosome 15
Chromosome location 15q14
miRNA miRNA information provided by mirtarbase database.
56
miRTarBase ID miRNA Experiments Reference
MIRT020544 hsa-miR-155-5p Proteomics 18668040
MIRT045397 hsa-miR-149-5p CLASH 23622248
MIRT721433 hsa-miR-4728-3p HITS-CLIP 19536157
MIRT721432 hsa-miR-4762-5p HITS-CLIP 19536157
MIRT721431 hsa-miR-29a-5p HITS-CLIP 19536157
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
19
GO ID Ontology Definition Evidence Reference
GO:0003723 Function RNA binding HDA 22658674, 22681889
GO:0005515 Function Protein binding IPI 24608264, 28040436, 30021884
GO:0005634 Component Nucleus IDA 24608264
GO:0005634 Component Nucleus IEA
GO:0005634 Component Nucleus NAS 21311021
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616142 26773 ENSG00000171262
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q52LJ0
Protein name Protein FAM98B
Protein function Positively stimulates PRMT1-induced protein arginine dimethylated arginine methylation (PubMed:28040436).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF10239 DUF2465 17 331 Protein of unknown function (DUF2465) Family
Tissue specificity TISSUE SPECIFICITY: Expressed strongly in colorectal cancer tissues compared to wild-type colon samples (at protein level) (PubMed:28040436). Expressed strongly in colorectal cancer tissues compared to wild-type colon samples (PubMed:28040436). {ECO:00002
Sequence
Sequence length 433
Interactions View interactions
Pathways Pathway information has different metabolic/signaling pathways associated with genes.
  Reactome
    tRNA processing in the nucleus
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
PSYCHOSIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
SYSTEMIC LUPUS ERYTHEMATOSUS GWAS catalog
★★☆☆☆
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
Lupus Erythematosus, Systemic Lupus Erythematosus GWASDB_DG 24871463
★☆☆☆☆
Found in Text Mining only
Lupus Erythematosus, Systemic Lupus Erythematosus GWASCAT_DG 24871463
★☆☆☆☆
Found in Text Mining only