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
RS1555868362 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS1555883949 Health Risk Pathogenic See cases, See cases
RS1555889131 Health Risk Pathogenic Pseudopseudohypoparathyroidism, Inborn genetic diseases, Gastric cancer
RS1555891743 Health Risk Pathogenic
RS1569020396 Health Risk Pathogenic
RS1601115202 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism
RS1601115231 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism
RS1601163749 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Progressive osseous heteroplasia
RS1601164303 Health Risk Pathogenic
RS1601164378 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism
RS1601166850 Health Risk Pathogenic
RS2089384365 Health Risk Pathogenic 8 conditions, GNAS-related disorder, 8 conditions
RS2089386059 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2089393181 Health Risk Pathogenic Pseudohypoparathyroidism type 1B, Pseudohypoparathyroidism type 1B
RS2090829910 Health Risk Pathogenic Pseudohypoparathyroidism type 1B, Pseudohypoparathyroidism type 1B
RS2090848106 Health Risk Pathogenic Pseudohypoparathyroidism type I A, 8 conditions, GNAS-related disorder
RS2091270014 Health Risk Pathogenic
RS2091272733 Health Risk Pathogenic
RS2091303526 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2091380655 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism
RS2145914268 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2145914732 Health Risk Pathogenic
RS2145916486 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism
RS2145916749 Health Risk Pathogenic Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism
RS2145916888 Health Risk Pathogenic Pseudohypoparathyroidism type I A, GNAS-related disorder, Inborn genetic diseases
RS2145916985 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2145917348 Health Risk Pathogenic
RS2146005743 Health Risk Pathogenic
RS2146079806 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudohypoparathyroidism
RS2146178007 Health Risk Pathogenic
RS2146178462 Health Risk Pathogenic Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism
RS2146178942 Health Risk Pathogenic
RS2146182909 Health Risk Pathogenic
RS2146185615 Health Risk Pathogenic
RS2146185827 Health Risk Pathogenic
RS2146208325 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2146209197 Health Risk Pathogenic
RS2146210053 Health Risk Pathogenic Inborn genetic diseases, Inborn genetic diseases
RS2146210932 Health Risk Pathogenic
RS2146270332 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2146270735 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2146271310 Health Risk Pathogenic Pseudopseudohypoparathyroidism, Pseudohypoparathyroidism, Pseudopseudohypoparathyroidism
RS2146272015 Health Risk Pathogenic
RS2146278555 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type 1B, GNAS-related disorder
RS2146283488 Health Risk Pathogenic Pseudohypoparathyroidism type I A, Pseudohypoparathyroidism type I A
RS2146290056 Health Risk Pathogenic Pseudohypoparathyroidism, Progressive osseous heteroplasia, Pseudohypoparathyroidism
RS2146292463 Health Risk Pathogenic Pseudohypoparathyroidism type I A, GNAS-related disorder, Pseudohypoparathyroidism type I A
RS2146292888 Health Risk Pathogenic
RS2146300173 Health Risk Pathogenic
RS2146300427 Health Risk Pathogenic 8 conditions, 8 conditions
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