Entity Details

Primary name CLCF1
Entity type gene
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Details

PrimaryID23529
RefseqGeneNG_013377
SymbolCLCF1
Namecardiotrophin like cytokine factor 1
Chromosome11
Location11q13.2
TaxID9606
Statuslive
SourceGenomegenomic
SourceOriginnatural
CreationDate2000-03-05
ModificationDate2021-06-11

Ontological Relatives

UniProt IDsCLCF1_HUMAN

GO terms

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GOName
GO:0002639 positive regulation of immunoglobulin production
GO:0005102 signaling receptor binding
GO:0005125 cytokine activity
GO:0005127 ciliary neurotrophic factor receptor binding
GO:0005576 extracellular region
GO:0007166 cell surface receptor signaling pathway
GO:0007259 receptor signaling pathway via JAK-STAT
GO:0008083 growth factor activity
GO:0008284 positive regulation of cell population proliferation
GO:0019221 cytokine-mediated signaling pathway
GO:0030183 B cell differentiation
GO:0030890 positive regulation of B cell proliferation
GO:0042531 positive regulation of tyrosine phosphorylation of STAT protein
GO:0043524 negative regulation of neuron apoptotic process
GO:0048295 positive regulation of isotype switching to IgE isotypes
GO:0048711 positive regulation of astrocyte differentiation
GO:0097058 CRLF-CLCF1 complex
GO:0097059 CNTFR-CLCF1 complex

Diseases

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Disease IDSourceNameDescription
610313 OMIMCrisponi/Cold-induced sweating syndrome 2 (CISS2)An autosomal recessive disorder characterized by profuse sweating induced by cool surroundings (temperatures of 7 to 18 degrees Celsius). Patients manifest, in the neonatal period, orofacial weakness with impaired sucking and swallowing, resulting in poor feeding. Affected infants show a tendency to startle, with contractions of the facial muscles in response to tactile stimuli or during crying, trismus, abundant salivation, and opisthotonus. These features are referred to as Crisponi syndrome and can result in early death in infancy. Patients who survive into childhood have hyperhidrosis, mainly of the upper body, in response to cold temperatures, and sweat very little with heat. Additional abnormalities include a high-arched palate, nasal voice, depressed nasal bridge, inability to fully extend the elbows and kyphoscoliosis. The disease is caused by variants affecting the gene represented in this entry.