Homo sapiens Protein: FAM89B
Summary
InnateDB Protein IDBP-57297.5
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol FAM89B
Protein Name family with sequence similarity 89, member B
Synonyms LRAP25; MTVR1;
Species Homo sapiens
Ensembl Protein ENSP00000314829
InnateDB Gene IDBG-57295 (FAM89B)
Protein Structure
UniProt Annotation
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. {ECO:0000250}.
Subcellular Localization Isoform 3: Cytoplasm {ECO:0000250}.Isoform 1: Cell surface {ECO:0000250}.
Disease Associations
Tissue Specificity
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0001222 transcription corepressor binding
Biological Process
GO:0030512 negative regulation of transforming growth factor beta receptor signaling pathway
GO:0060392 negative regulation of SMAD protein import into nucleus
Cellular Component
GO:0005737 cytoplasm
GO:0009986 cell surface
Protein Structure and Domains
PDB ID
InterPro
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q8N5H3
PhosphoSite PhosphoSite-Q8N5H3
TrEMBL
UniProt Splice Variant
Entrez Gene 23625
UniGene
RefSeq NP_690045
HUGO HGNC:16708
OMIM
CCDS CCDS8105
HPRD 10100
IMGT
EMBL AF052151 AP001362 BC023991 BC032373 BM557093
GenPept AAH23991 AAH32373