Homo sapiens Protein: CNTF
Summary
InnateDB Protein IDBP-47875.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol CNTF
Protein Name ciliary neurotrophic factor
Synonyms HCNTF;
Species Homo sapiens
Ensembl Protein ENSP00000355370
InnateDB Gene IDBG-409278 (CNTF)
Protein Structure
UniProt Annotation
Function CNTF is a survival factor for various neuronal cell types. Seems to prevent the degeneration of motor axons after axotomy.
Subcellular Localization Cytoplasm.
Disease Associations
Tissue Specificity Nervous system.
Comments
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 16 experimentally validated interaction(s) in this database.
They are also associated with 3 interaction(s) predicted by orthology.
Experimentally validated
Total 16 [view]
Protein-Protein 16 [view]
Protein-DNA 0
Protein-RNA 0
DNA-DNA 0
RNA-RNA 0
DNA-RNA 0
Predicted by orthology
Total 3 [view]
Gene Ontology

Molecular Function
Accession GO Term
GO:0005127 ciliary neurotrophic factor receptor binding
GO:0005138 interleukin-6 receptor binding
GO:0008083 growth factor activity
Biological Process
GO:0007165 signal transduction
GO:0008284 positive regulation of cell proliferation
GO:0040007 growth
GO:0042517 positive regulation of tyrosine phosphorylation of Stat3 protein
GO:0043524 negative regulation of neuron apoptotic process
GO:0046533 negative regulation of photoreceptor cell differentiation
GO:0046668 regulation of retinal cell programmed cell death
GO:0048644 muscle organ morphogenesis
GO:0048666 neuron development
GO:0070120 ciliary neurotrophic factor-mediated signaling pathway
Cellular Component
GO:0005615 extracellular space
GO:0005737 cytoplasm
GO:0097058 CRLF-CLCF1 complex
Protein Structure and Domains
PDB ID
InterPro IPR000151 Ciliary neurotrophic factor, CNTF
IPR009079 Four-helical cytokine-like, core
PFAM PF01110
PRINTS
PIRSF
SMART
TIGRFAMs
Post-translational Modifications
Modification
Cross-References
SwissProt P26441
PhosphoSite PhosphoSite-
TrEMBL
UniProt Splice Variant
Entrez Gene 1270
UniGene
RefSeq NP_000605
HUGO HGNC:2169
OMIM 118945
CCDS CCDS31554
HPRD 00347
IMGT
EMBL AK314118 BC068030 BC074963 BC074964 CH471076 X55889 X55890 X60477 X60478 X60542
GenPept AAH68030 AAH74963 AAH74964 BAG36809 CAA39374 CAA43009 CAA43032 EAW73819