The GNAS gene homepage

General information
Gene symbol GNAS
Gene name GNAS complex locus
Chromosome 20
Chromosomal band q13.2-q13.3
Imprinted Unknown
Genomic reference NG_016194.1
Transcript reference NM_000516.4, NM_001077488.2, NM_001077489.2, NM_001077490.1, NM_016592.2, NM_080425.2, NM_080426.2, NR_003259.1, XM_005260396.1, XM_005260397.1, XM_005260398.1, XM_005260399.1, XM_005260400.1, XM_005260401.1, XM_005260402.1
Associated with diseases AIMAH-1, ID, MAS, PAGH-1, PHP-1A, PHP-1B, PHP-1C, POH, PPHP, bleeding time, prolonged, brachydactyly and mental retardation
Citation reference(s) -
Curators (1) Johan T. den Dunnen
Total number of public variants reported 91
Unique public DNA variants reported 20
Individuals with public variants 35
Hidden variants 121
Date created December 09, 2013
Date last updated September 28, 2016
Version GNAS:160928

Graphical displays and utilities
Graphs Graphs displaying summary information of all variants in the database »
UCSC Genome Browser Show variants in the UCSC Genome Browser (full view, compact view)
Ensembl Genome Browser Show variants in the Ensembl Genome Browser (full view, compact view)
NCBI Sequence Viewer Show distribution histogram of variants in the NCBI Sequence Viewer

Links to other resources
External URL List of LSDBs for this gene
The reference LOVD for this gene, if available
HGNC HGNC:4392
Entrez Gene 2778
PubMed articles GNAS
OMIM - Gene 139320
OMIM - Diseases AIMAH-1 (hyperplasia, adrenal, ACTH-independent, macronodular, type 1 (AIMAH-1))
MAS (POFD)
PAGH-1 (adenoma, pituitary, growth hormone-secreting, type 1 (PAGH-1, acromegaly))
PHP-1A (pseudohypoparathyroidism, type Ia (PHP-1A, Albright hereditary osteodystrophy (AHO)))
PHP-1B (pseudohypoparathyroidism, type Ib (PHP-1B))
PHP-1C (pseudohypoparathyroidism, type Ic (PHP-1C))
POH (heteroplasia, osseous, progressive (POH))
PPHP (pseudopseudohypoparathyroidism (PPHP))
HGMD GNAS
GeneCards GNAS
GeneTests GNAS


Active transcripts


ID     

Chr     

Name     

NCBI ID     

NCBI Protein ID     

DescendingVariants     
00017281 20 Manually created transcript. NM_016592.2 - 72
00017280 20 Manually created transcript. (removed from reference sequence) NM_001077490.1 - 56
00017282 20 Manually created transcript. NM_080425.2 - 56
00017277 20 Manually created transcript. (removed from reference sequence) NM_000516.4 - 43
00017278 20 Manually created transcript. (removed from reference sequence) NM_001077488.2 - 43
00017279 20 Manually created transcript. NM_001077489.2 - 43
00017283 20 Manually created transcript. (removed from reference sequence) NM_080426.2 - 43
00042050 20 transcript variant X4 XM_005260399.1 - -
00042051 20 transcript variant X2 XM_005260397.1 XP_005260454.1 -
00042052 20 transcript variant X3 XM_005260398.1 - -
00042053 20 transcript variant X5 XM_005260400.1 - -
00042054 20 transcript variant X1 XM_005260396.1 - -
00042055 20 transcript variant X7 XM_005260402.1 XP_005260459.1 -
00042056 20 transcript variant X6 XM_005260401.1 XP_005260458.1 -
00042057 20 transcript variant 8 NR_003259.1 - -


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