GNAS Chromosome 20
GNAS complex locus
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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
RS111796234
Conflicting classifications of pathogenicity
GNAS-related disorder, GNAS-related disorder
Health Risk
RS1135401777
Conflicting classifications of pathogenicity
Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism
Health Risk
RS11554274
Conflicting classifications of pathogenicity
Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
Health Risk
RS1272546759
Conflicting classifications of pathogenicity
Pseudopseudohypoparathyroidism, Pseudopseudohypoparathyroidism
Health Risk
RS137854535
Conflicting classifications of pathogenicity
Pseudopseudohypoparathyroidism, Inborn genetic diseases, Pseudohypoparathyroidism type I A
Health Risk
RS137854537
Conflicting classifications of pathogenicity
PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
Health Risk
RS1446835451
Conflicting classifications of pathogenicity
Health Risk
RS146581290
Conflicting classifications of pathogenicity
GNAS-related disorder, GNAS-related disorder
Health Risk
RS1555889031
Conflicting classifications of pathogenicity
Health Risk
RS1569027992
Conflicting classifications of pathogenicity
8 conditions, 8 conditions
Health Risk
RS1600976255
Conflicting classifications of pathogenicity
Pseudohypoparathyroidism, Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type 1B
Health Risk
RS199499878
Conflicting classifications of pathogenicity
GNAS-related disorder, GNAS-related disorder
Health Risk
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 |