GNAS (Gene)

Synonyms:AHO, C20orf45, ENTREZ:2778, GNAS complex locus, GNAS, GNAS1, GPSA, GSA, GSP, HGNC:4392, MIM:139320, NESP, NM_000516, NM_001077488, NM_001077489, NM_001077490, NM_001309840, NM_001309842, NM_001309861, NM_001309883, NM_016592, NM_080425, NM_080426, NP_000507, NP_001070956, NP_001070957, NP_001070958, NP_001296769, NP_001296771, NP_001296790, NP_001296812, NP_057676, NP_536350, NP_536351, NR_132272, NR_132273, PITA3, POH, SCG6, SgVI, XM_017027812, XM_017027813, XM_017027814, XM_017027815, XM_017027816, XM_017027817, XM_017027818, XM_017027819, XM_017027820, XM_017027821, XM_017027822, XM_024451872, XM_024451873, XM_024451874, XM_024451875, XP_016883301, XP_016883302, XP_016883303, XP_016883304, XP_016883305, XP_016883306, XP_016883307, XP_016883308, XP_016883309, XP_016883310, XP_016883311, XP_024307640, XP_024307641, XP_024307642, XP_024307643, XR_002958471
Omim:OMIM:139320
Id:ENSG00000087460
Hgnc:HGNC:4392
Entrez:2778
Description:GNAS complex locus
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]

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Data Distillery
CFDE DD-Knowledge Graph

The CFDE Data Distillery Knowledge Graph contains entities and relationships across the CFDE. View GNAS's neighborhood in the knowledge graph.

Playbook Workflow Builder
Playbook Workflow Builder: Gene-Centric Workflow

View Gene-Centric information about the gene from a pre-built PWB workflow. View the workflow with GNAS.

Gene Partnership Appyter
CFDE Gene-Centric Appyter

The CFDE Gene Centric Appyter Resolves and Displays Gene-Centric information from CFDE APIs. Execute the Appyter using GNAS.

Gene and Drug Landing Page Aggregator
GDLPA Landing Pages Links

The Gene and Drug Landing Page Aggregator (GDLPA) finds links to primary and secondary source information from CFDE and other resources. Discover landing pages for GNAS.

Playbook Workflow Builder
Playbook Workflow Builder

The Playbook Workflow Builder helps you interactively construct workflows leveraging CFDE APIs without code. Start a new workflow with GNAS.

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