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
RS111796234 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS1135401777 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism
RS11554274 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS1272546759 Health Risk Conflicting classifications of pathogenicity Pseudopseudohypoparathyroidism, Pseudopseudohypoparathyroidism
RS137854535 Health Risk Conflicting classifications of pathogenicity Pseudopseudohypoparathyroidism, Inborn genetic diseases, Pseudohypoparathyroidism type I A
RS137854537 Health Risk Conflicting classifications of pathogenicity PSEUDOHYPOPARATHYROIDISM, TYPE IA, WITH TESTOTOXICOSIS
RS1446835451 Health Risk Conflicting classifications of pathogenicity
RS146581290 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS1555889031 Health Risk Conflicting classifications of pathogenicity
RS1569027992 Health Risk Conflicting classifications of pathogenicity 8 conditions, 8 conditions
RS1600976255 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism, Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type 1B
RS199499878 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS200409817 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS201290965 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism type 1B, Pseudohypoparathyroidism type 1C, Pseudopseudohypoparathyroidism
RS201332059 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS201597085 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, 8 conditions, GNAS-related disorder
RS2090976492 Health Risk Conflicting classifications of pathogenicity
RS2091273769 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, Albright hereditary osteodystrophy, pseudohypoparathyroidism
RS2146184314 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2146208770 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism type I A, GNAS-related disorder, Pseudohypoparathyroidism type I A
RS2146210724 Health Risk Conflicting classifications of pathogenicity
RS2146291027 Health Risk Conflicting classifications of pathogenicity
RS2517226164 Health Risk Conflicting classifications of pathogenicity
RS527488103 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, 8 conditions, GNAS-related disorder
RS563844600 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS576071932 Health Risk Conflicting classifications of pathogenicity Malignant tumor of esophagus, Familial cancer of breast, Malignant tumor of esophagus
RS587778383 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS745433225 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS747093000 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS747759524 Health Risk Conflicting classifications of pathogenicity GNAS-related disorder, GNAS-related disorder
RS763548893 Health Risk Conflicting classifications of pathogenicity
RS767104257 Health Risk Conflicting classifications of pathogenicity Pseudohypoparathyroidism type 1B, Pseudohypoparathyroidism type 1C, Pseudohypoparathyroidism type I A
RS771111377 Health Risk Conflicting classifications of pathogenicity
RS776846313 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, GNAS-related disorder, Inborn genetic diseases
RS1057520715 Health Risk Likely pathogenic
RS1064795798 Health Risk Likely pathogenic
RS111541229 Health Risk Likely pathogenic
RS1555891562 Health Risk Likely pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1555891584 Health Risk Likely pathogenic GNAS-related disorder, Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS1555891595 Health Risk Likely pathogenic Inborn genetic diseases, GNAS-related disorder, Inborn genetic diseases
RS1555891728 Health Risk Likely pathogenic
RS1569015549 Health Risk Likely pathogenic Pseudopseudohypoparathyroidism, Pseudopseudohypoparathyroidism
RS1569031388 Health Risk Likely pathogenic
RS1569032751 Health Risk Likely pathogenic McCune-Albright syndrome, Pseudohypoparathyroidism type 1B, McCune-Albright syndrome
RS2085661524 Health Risk Likely pathogenic Pseudopseudohypoparathyroidism, Pseudopseudohypoparathyroidism
RS2086303843 Health Risk Likely pathogenic Intellectual disability, Pseudohypoparathyroidism, Intellectual disability
RS2089376607 Health Risk Likely pathogenic
RS2089974938 Health Risk Likely pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism
RS2090974560 Health Risk Likely pathogenic
RS2091331588 Health Risk Likely pathogenic Pseudopseudohypoparathyroidism, Pseudopseudohypoparathyroidism
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