GNA13

Protein-coding gene in the species Homo sapiens From Wikipedia, the free encyclopedia

Guanine nucleotide-binding protein subunit alpha-13 is a protein that in humans is encoded by the GNA13 gene.[5][6]

PDBOrtholog search: PDBe RCSB
AliasesGNA13, G13, G protein subunit alpha 13, HG1N
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GNA13
Available structures
PDBOrtholog search: PDBe RCSB
Identifiers
AliasesGNA13, G13, G protein subunit alpha 13, HG1N
External IDsOMIM: 604406; MGI: 95768; HomoloGene: 55976; GeneCards: GNA13; OMA:GNA13 - orthologs
Orthologs
SpeciesHumanMouse
Entrez
Ensembl
UniProt
RefSeq (mRNA)

NM_001282425
NM_006572

NM_010303
NM_001359034

RefSeq (protein)

NP_001269354
NP_006563

NP_034433
NP_001345963

Location (UCSC)Chr 17: 65.01 – 65.06 MbChr 11: 109.25 – 109.29 Mb
PubMed search[3][4]
Wikidata
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Interactions and functions

The GNA13 gene encodes the G13 G protein alpha subunit. Together with GNA12, these two proteins comprise one of the four classes of heterotrimeric G protein alpha subunits.[7] Heterotrimeric G proteins function in transducing hormone and neurotransmitter signals detected by cell surface G protein-coupled receptors to intracellular signaling pathways to modulate cell functions. G protein alpha subunits bind to guanine nucleotides and function in a regulatory cycle, and are active when bound to GTP but inactive and associated with the G beta-gamma complex when bound to GDP.[8][9]

Active GTP-bound G12 alpha subunit interacts with and activates ARHGEF1,[10][11][12] ARHGEF11,[13][14] and ARHGEF12.[15][16] These ARHGEF proteins function as guanine nucleotide exchange factors for the Rho small GTPases to regulate the actin cytoskeleton.[17]

GNA13 has been shown to interact with AKAP3,[18] RIC8A,[19][20] and Radixin.[21]

Clinical significance

Recurrent mutations in this gene have been associated to cases of diffuse large B-cell lymphoma.[22][23]

See also

References

Further reading

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