LIFR Chromosome 5

LIF receptor subunit alpha
157 variants 157 Health Risk

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What This Gene Does
This gene encodes a protein that belongs to the type I cytokine receptor family. This protein combines with a high-affinity converter subunit, gp130, to form a receptor complex that mediates the action of the leukemia inhibitory factor, a polyfunctional cytokine that is involved in cellular differentiation, proliferation and survival in the adult and the embryo. Mutations in this gene cause Schwartz-Jampel syndrome type 2, a disease belonging to the group of the bent-bone dysplasias. A translocation that involves the promoter of this gene, t(5;8)(p13;q12) with the pleiomorphic adenoma gene 1, is associated with salivary gland pleiomorphic adenoma, a common type of benign epithelial tumor of the salivary gland. Multiple splice variants encoding two different isoforms have been found for this gene. [provided by RefSeq, Jun 2018]
Gene Info
Gene Group
"CD molecules|Fibronectin type III domain containing|MicroRNA protein coding host genes"
Locus Type
gene with protein product
Location
5p13.1
Ensembl
ENSG00000113594
Associated Conditions (8)
Stuve-Wiedemann syndrome
Connective tissue disorder
Stüve-Wiedemann syndrome 1
LIFR-related disorder
Inborn genetic diseases
Congenital anomaly of kidney and urinary tract
Ovarian serous cystadenocarcinoma
Cervical cancer
Key Variants
RS1195064309
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS139809889
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS139848756
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Connective tissue disorder, Stüve-Wiedemann syndrome 1
Health Risk
RS140538535
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, LIFR-related disorder, Stuve-Wiedemann syndrome
Health Risk
RS141407987
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS1424683209
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS144332222
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS145163157
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
Health Risk
RS147058538
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Inborn genetic diseases, Stüve-Wiedemann syndrome 1
Health Risk
RS148354076
Conflicting classifications of pathogenicity
Stuve-Wiedemann syndrome, Connective tissue disorder, Stüve-Wiedemann syndrome 1
Health Risk
RS151282774
Conflicting classifications of pathogenicity
LIFR-related disorder, LIFR-related disorder
Health Risk
RS1561179800
Conflicting classifications of pathogenicity
Stüve-Wiedemann syndrome 1, Stüve-Wiedemann syndrome 1
Health Risk
All Variants (157)
RSID Category Clinical Significance Conditions
RS758055364 Health Risk Pathogenic/Likely pathogenic Cervical cancer, Stüve-Wiedemann syndrome 1, Cervical cancer
RS765602627 Health Risk Pathogenic/Likely pathogenic Stüve-Wiedemann syndrome 1, Stüve-Wiedemann syndrome 1
RS765622323 Health Risk Pathogenic/Likely pathogenic Stuve-Wiedemann syndrome, Stüve-Wiedemann syndrome 1, Stuve-Wiedemann syndrome
RS773896661 Health Risk Pathogenic/Likely pathogenic Stüve-Wiedemann syndrome 1, Stüve-Wiedemann syndrome 1
RS779829941 Health Risk Pathogenic/Likely pathogenic Stuve-Wiedemann syndrome, Stüve-Wiedemann syndrome 1, Stuve-Wiedemann syndrome
RS863225047 Health Risk Pathogenic/Likely pathogenic Stuve-Wiedemann syndrome, Stuve-Wiedemann syndrome
RS886041545 Health Risk Pathogenic/Likely pathogenic Stüve-Wiedemann syndrome 1, Stüve-Wiedemann syndrome 1
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