Homo sapiens Protein: C9orf89
Summary
InnateDB Protein IDBP-596504.2
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C9orf89
Protein Name chromosome 9 open reading frame 89
Synonyms
Species Homo sapiens
Ensembl Protein ENSP00000437237
InnateDB Gene IDBG-76473 (C9orf89)
Protein Structure
UniProt Annotation
Function Plays a role in inhibiting the effects of BCL10-induced activation of NF-kappa-B. May inhibit the phosphorylation of BCL10 in a CARD-dependent manner. {ECO:0000269PubMed:15637807}.
Subcellular Localization Isoform 1: Nucleus {ECO:0000269PubMed:23633586}. Note=Coexpression with BCL10 induced translocation from nucleus to cytosol.Isoform 2: Endoplasmic reticulum membrane {ECO:0000269PubMed:23633586}; Single-pass membrane protein {ECO:0000269PubMed:23633586}. Mitochondrion membrane {ECO:0000269PubMed:23633586}; Single-pass membrane protein {ECO:0000269PubMed:23633586}.
Disease Associations
Tissue Specificity Expressed in ovary, testis, placenta, skeletal muscle, kidney, lung, heart and liver (at protein level). Expressed in thymus and brain. {ECO:0000269PubMed:15637807}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 4 experimentally validated interaction(s) in this database.
Experimentally validated
Total 4 [view]
Protein-Protein 3 [view]
Protein-DNA 1 [view]
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0050700 CARD domain binding
Biological Process
GO:0043124 negative regulation of I-kappaB kinase/NF-kappaB signaling
Cellular Component
GO:0005634 nucleus
GO:0005789 endoplasmic reticulum membrane
GO:0005794 Golgi apparatus
GO:0005829 cytosol
GO:0016021 integral component of membrane
GO:0031966 mitochondrial membrane
Protein Structure and Domains
PDB ID
InterPro IPR011029 Death-like domain
PFAM
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q96LW7
PhosphoSite PhosphoSite-Q96LW7
TrEMBL
UniProt Splice Variant
Entrez Gene 84270
UniGene Hs.434213
RefSeq
HUGO HGNC:28148
OMIM
CCDS
HPRD 12985
IMGT
EMBL AK057716 AL451065 BC004500 BC038856
GenPept AAH04500 AAH38856 BAB71550 CAI95110