Homo sapiens Protein: C11orf9
Summary
InnateDB Protein IDBP-50297.7
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol C11orf9
Protein Name chromosome 11 open reading frame 9
Synonyms C11orf9; MRF; Ndt80; pqn-47;
Species Homo sapiens
Ensembl Protein ENSP00000265460
InnateDB Gene IDBG-50293 (C11orf9)
Protein Structure
UniProt Annotation
Function Myelin regulatory factor: Consitutes a precursor of the transcription factor. Mediates the autocatalytic cleavage that releases the Myelin regulatory factor, N-terminal component that specifically activates transcription of central nervous system (CNS) myelin genes (PubMed:23966832). {ECO:0000269PubMed:23966832}.Myelin regulatory factor, C-terminal: Membrane-bound part that has no transcription factor activity and remains attached to the endoplasmic reticulum membrane following cleavage. {ECO:0000269PubMed:23966832}.Myelin regulatory factor, N-terminal: Transcription factor that specifically activates expression of myelin genes such as MBP, MOG, MAG and PLP1 during oligodendrocyte (OL) maturation, thereby playing a central role in oligodendrocyte maturation and CNS myelination. Specifically recognizes and binds DNA sequence 5'-CTGGYAC-3' in the regulatory regions of myelin-specific genes and directly activates their expression. Not only required during oligodendrocyte differentiation but is also required on an ongoing basis for the maintenance of expression of myelin genes and for the maintenance of a mature, viable oligodendrocyte phenotype (PubMed:23966832). {ECO:0000269PubMed:23966832}.
Subcellular Localization Myelin regulatory factor: Endoplasmic reticulum membrane; Single-pass membrane protein.Myelin regulatory factor, N-terminal: Nucleus. Cytoplasm. Note=Translocates from the cytoplasm to the nucleus upon autocatalytic cleavage.Myelin regulatory factor, C-terminal: Endoplasmic reticulum membrane; Single-pass membrane protein.
Disease Associations
Tissue Specificity Expressed in lung, ARPE-19 cell line, brainstem, uterus and, to a lesser extent, in basal ganglion and liver. Weakly expressed in cerebellum and retina. {ECO:0000269PubMed:10828591}.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 1 experimentally validated interaction(s) in this database.
Experimentally validated
Total 1 [view]
Protein-Protein 1 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Gene Ontology

Molecular Function
Accession GO Term
GO:0003677 DNA binding
GO:0003700 sequence-specific DNA binding transcription factor activity
GO:0008233 peptidase activity
Biological Process
GO:0006351 transcription, DNA-templated
GO:0006355 regulation of transcription, DNA-templated
GO:0006508 proteolysis
GO:0014003 oligodendrocyte development
GO:0022010 central nervous system myelination
GO:0031643 positive regulation of myelination
GO:0032286 central nervous system myelin maintenance
GO:0045893 positive regulation of transcription, DNA-templated
GO:0048709 oligodendrocyte differentiation
Cellular Component
GO:0005634 nucleus
GO:0005789 endoplasmic reticulum membrane
GO:0016021 integral component of membrane
Protein Structure and Domains
PDB ID
InterPro IPR008967 p53-like transcription factor, DNA-binding
IPR024061 NDT80 DNA-binding domain
PFAM PF05224
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt Q9Y2G1
PhosphoSite PhosphoSite-Q9Y2G1
TrEMBL
UniProt Splice Variant
Entrez Gene 745
UniGene Hs.682698
RefSeq NP_037411
HUGO HGNC:1181
OMIM 608329
CCDS CCDS31579
HPRD 12213
IMGT
EMBL AB023171 AF038536 AF086762 CH471076
GenPept AAB92668 AAF28400 BAA76798 EAW73968