Details

Home Details


Basic information of CNTF :

Official Symbol of Gene CNTF
Species Homo sapiens
Entrez Gene ID 1270
Official Full Name ciliary neurotrophic factor
Also known as HCNTF
Gene Type protein coding
dbXrefs Ensembl:ENSG00000242689 MIM:118945; AllianceGenome:HGNC:2169
Map Location 11q12.1
Variation Type mutation
refSNP ID N/A

Sample information of multiple sclerosis:

Detected Sample blood
Sample Detail N/A
Detected Method PCR
Disease MS
Disease subtype RRMS,PPMS,SPMS
Population N/A
Sample Size 349 MS / 434 healthy controls

Literature information of multiple sclerosis :

Pubmed ID 11857064
Year 2002
Title A null mutation within the ciliary neurotrophic factor (CNTF)-gene: implications for susceptibility and disease severity in patients with multiple sclerosis

Results of multiple sclerosis :

Risk Type Phenotypic risk
Main Result Negative
Result The frequency of patients with early or late onset of the disease and clinical course of RRMS, SPMS or PPMS was not different in patients homozygous for the CNTF 01 allele or those heterozygous for the CNTF alleles 01 and 02.The CNTF-genotype was not correlated with disease progression, ie, similar frequencies were obtained for patients classified as having less severe, moderately severe or severe MS.
Mechanism/Pathway While CNTF was initially characterized as a trophic factor for neurons5–7 more recent evidence supports the role for survival, proliferation, and maturation of oligodendrocyte lineage cells.In addition CNTF protects oligodendrocytes from TNF-α induced cell death and was found to be increased in cerebrospinal fluid (CSF) of MS patients recovering from acute exacerbations.