Gene Gene information from NCBI Gene database.
Entrez ID 23625
Gene name Family with sequence similarity 89 member B
Gene symbol FAM89B
Synonyms (NCBI Gene)
LRAP25MTVRMTVR1
Chromosome 11
Chromosome location 11q13.1
miRNA miRNA information provided by mirtarbase database.
87
miRTarBase ID miRNA Experiments Reference
MIRT025771 hsa-miR-7-5p Microarray 19073608
MIRT038867 hsa-miR-93-3p CLASH 23622248
MIRT988437 hsa-miR-1233 CLIP-seq
MIRT988438 hsa-miR-1280 CLIP-seq
MIRT988439 hsa-miR-1293 CLIP-seq
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
22
GO ID Ontology Definition Evidence Reference
GO:0001222 Function Transcription corepressor binding IBA
GO:0001222 Function Transcription corepressor binding IEA
GO:0001222 Function Transcription corepressor binding ISS
GO:0005737 Component Cytoplasm IBA
GO:0005737 Component Cytoplasm IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
616128 16708 ENSG00000176973
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q8N5H3
Protein name Leucine repeat adapter protein 25
Protein function Negatively regulates TGF-beta-induced signaling; in cooperation with SKI prevents the translocation of SMAD2 from the nucleus to the cytoplasm in response to TGF-beta. Acts as an adapter that mediates the specific recognition of LIMK1 by CDC42BP
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF14854 LURAP 75 152 Leucine rich adaptor protein Family
Sequence
MNGLPSAEAPGGAGCALAGLPPLPRGLSGLLNASGGSWRELERVYSQRSRIHDELSRAAR
APDGPRHAAGAANAGPAAGPRRPVNLDSALAALRKEMVGLRQLDMSLLCQLWGLYESIQD
YKHLCQDLSFCQDLSSSLHSDSSYPPDAGLSD
DEEPPDASLPPDPPPLTVPQTHNARDQW
LQDAFHISL
Sequence length 189
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
OSTEOARTHRITIS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OSTEOARTHRITIS, HIP GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations