Entity Details

Primary name CRLF1_HUMAN
Entity type UniProt
Source Source Link

Details

AccessionO75462
EntryNameCRLF1_HUMAN
FullNameCytokine receptor-like factor 1
TaxID9606
Evidenceevidence at protein level
Length422
SequenceStatuscomplete
DateCreated2004-03-01
DateModified2021-06-02

Ontological Relatives

GenesCRLF1

GO terms

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GOName
GO:0001657 ureteric bud development
GO:0004896 cytokine receptor activity
GO:0005576 extracellular region
GO:0005615 extracellular space
GO:0005829 cytosol
GO:0008284 positive regulation of cell population proliferation
GO:0009897 external side of plasma membrane
GO:0019221 cytokine-mediated signaling pathway
GO:0019955 cytokine binding
GO:0042531 positive regulation of tyrosine phosphorylation of STAT protein
GO:0043235 receptor complex
GO:0043524 negative regulation of neuron apoptotic process
GO:0070106 interleukin-27-mediated signaling pathway
GO:0097058 CRLF-CLCF1 complex
GO:2000672 negative regulation of motor neuron apoptotic process

Subcellular Location

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Subcellular Location
Secreted

Domains

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DomainNameCategoryType
IPR003961 Fibronectin type IIIDomainDomain
IPR013783 Immunoglobulin-like foldFamilyHomologous superfamily
IPR015152 Growth hormone/erythropoietin receptor, ligand bindingDomainDomain
IPR036116 Fibronectin type III superfamilyFamilyHomologous superfamily
IPR036179 Immunoglobulin-like domain superfamilyFamilyHomologous superfamily

Diseases

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Disease IDSourceNameDescription
272430 OMIMCrisponi/Cold-induced sweating syndrome 1 (CISS1)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.

Interactions

4 interactions