IL6ST Chromosome 5

Interleukin 6 cytokine family signal transducer
21 variants 21 Health Risk

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What This Gene Does
The protein encoded by this gene is a signal transducer shared by many cytokines, including interleukin 6 (IL6), ciliary neurotrophic factor (CNTF), leukemia inhibitory factor (LIF), and oncostatin M (OSM). This protein functions as a part of the cytokine receptor complex. The activation of this protein is dependent upon the binding of cytokines to their receptors. vIL6, a protein related to IL6 and encoded by the Kaposi sarcoma-associated herpesvirus, can bypass the interleukin 6 receptor (IL6R) and directly activate this protein. Knockout studies in mice suggest that this gene plays a critical role in regulating myocyte apoptosis. Alternatively spliced transcript variants have been described. A related pseudogene has been identified on chromosome 17. [provided by RefSeq, May 2014]
Gene Info
Gene Group
"CD molecules|Fibronectin type III domain containing|Interleukin receptors"
Locus Type
gene with protein product
Location
5q11.2
Ensembl
ENSG00000134352
Associated Conditions (8)
IL6ST-related disorder
Stuve-Wiedemann syndrome
Hyper-IgE recurrent infection syndrome 4
autosomal recessive
Stuve-Wiedemann syndrome 2
Hyper-IgE recurrent infection syndrome 4A
autosomal dominant
Immunodeficiency 94 with autoinflammation and dysmorphic facies
Key Variants
All Variants (21)
RSID Category Clinical Significance Conditions
RS141500365 Health Risk Conflicting classifications of pathogenicity
RS142901689 Health Risk Conflicting classifications of pathogenicity IL6ST-related disorder, IL6ST-related disorder
RS145020363 Health Risk Conflicting classifications of pathogenicity
RS145618093 Health Risk Conflicting classifications of pathogenicity
RS148372700 Health Risk Conflicting classifications of pathogenicity
RS1752049275 Health Risk Likely pathogenic
RS2533481097 Health Risk Likely pathogenic
RS1228531384 Health Risk Pathogenic
RS1579734448 Health Risk Pathogenic Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
RS1580801731 Health Risk Pathogenic Hyper-IgE recurrent infection syndrome 4, autosomal recessive, Hyper-IgE recurrent infection syndrome 4
RS1580809257 Health Risk Pathogenic Hyper-IgE recurrent infection syndrome 4, autosomal recessive, Hyper-IgE recurrent infection syndrome 4
RS1580817729 Health Risk Pathogenic Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome 2, Stuve-Wiedemann syndrome
RS2111585708 Health Risk Pathogenic Hyper-IgE recurrent infection syndrome 4A, autosomal dominant, Hyper-IgE recurrent infection syndrome 4A
RS2111585826 Health Risk Pathogenic Hyper-IgE recurrent infection syndrome 4A, autosomal dominant, Hyper-IgE recurrent infection syndrome 4A
RS2111587824 Health Risk Pathogenic Hyper-IgE recurrent infection syndrome 4A, autosomal dominant, Hyper-IgE recurrent infection syndrome 4A
RS2111677373 Health Risk Pathogenic Stuve-Wiedemann syndrome 2, Stuve-Wiedemann syndrome 2
RS2111774223 Health Risk Pathogenic Immunodeficiency 94 with autoinflammation and dysmorphic facies, Immunodeficiency 94 with autoinflammation and dysmorphic facies
RS2533477589 Health Risk Pathogenic
RS2533477700 Health Risk Pathogenic
RS2533484139 Health Risk Pathogenic
RS776023104 Health Risk Pathogenic
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