GNAS Chromosome 20

GNAS complex locus
206 variants 206 Health Risk

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What This Gene Does
This locus has a highly complex imprinted expression pattern. It gives rise to maternally, paternally, and biallelically expressed transcripts that are derived from four alternative promoters and 5' exons. Some transcripts contain a differentially methylated region (DMR) at their 5' exons, and this DMR is commonly found in imprinted genes and correlates with transcript expression. An antisense transcript is produced from an overlapping locus on the opposite strand. One of the transcripts produced from this locus, and the antisense transcript, are paternally expressed noncoding RNAs, and may regulate imprinting in this region. In addition, one of the transcripts contains a second overlapping ORF, which encodes a structurally unrelated protein - Alex. Alternative splicing of downstream exons is also observed, which results in different forms of the stimulatory G-protein alpha subunit, a key element of the classical signal transduction pathway linking receptor-ligand interactions with the activation of adenylyl cyclase and a variety of cellular reponses. Multiple transcript variants encoding different isoforms have been found for this gene. Mutations in this gene result in pseudohypoparathyroidism type 1a, pseudohypoparathyroidism type 1b, Albright hereditary osteodystrophy, pseudopseudohypoparathyroidism, McCune-Albright syndrome, progressive osseus heteroplasia, polyostotic fibrous dysplasia of bone, and some pituitary tumors. [provided by RefSeq, Aug 2012]
Gene Info
Gene Group
"Granins|G protein subunits alpha, group s"
Locus Type
gene with protein product
Location
20q13.32
Ensembl
ENSG00000087460
Associated Conditions (32)
GNAS-related disorder
Pseudohypoparathyroidism
Pseudopseudohypoparathyroidism
Pseudohypoparathyroidism type I A
Inborn genetic diseases
PSEUDOHYPOPARATHYROIDISM
TYPE IA
WITH TESTOTOXICOSIS
8 conditions
Pseudohypoparathyroidism type 1B
Progressive osseous heteroplasia
Pseudohypoparathyroidism type 1C
Albright hereditary osteodystrophy
pseudohypoparathyroidism
pseudopseudohypoparathyroidism
acrodysostosis and osteoma cutis
Malignant tumor of esophagus
Familial cancer of breast
McCune-Albright syndrome
Intellectual disability
+12 more conditions
Key Variants
All Variants (206)
RSID Category Clinical Significance Conditions
RS2516794697 Health Risk Pathogenic/Likely pathogenic Albright hereditary osteodystrophy, pseudohypoparathyroidism, pseudopseudohypoparathyroidism
RS2517082005 Health Risk Pathogenic/Likely pathogenic GNAS-associated disease, GNAS-associated disease
RS397514456 Health Risk Pathogenic/Likely pathogenic Pseudohypoparathyroidism type 1C, Pseudohypoparathyroidism type 1C, Pseudohypoparathyroidism type I A
RS587776829 Health Risk Pathogenic/Likely pathogenic Pseudohypoparathyroidism, Progressive osseous heteroplasia, Pseudopseudohypoparathyroidism
RS774711025 Health Risk Pathogenic/Likely pathogenic GNAS-related disorder, Pseudohypoparathyroidism type I A, Pseudopseudohypoparathyroidism
RS863224876 Health Risk Pathogenic/Likely pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism type 1C, Pseudohypoparathyroidism
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