Gene

gnaq

ID
ZDB-GENE-081104-25
Name
guanine nucleotide binding protein (G protein), q polypeptide
Symbol
gnaq Nomenclature History
Previous Names
  • gnaqa (1)
  • Galpha q (1)
  • si:ch73-270f14.2
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Predicted to enable several functions, including G-protein beta/gamma-subunit complex binding activity; GTPase activator activity; and GTPase activity. Predicted to be involved in adenylate cyclase-modulating G protein-coupled receptor signaling pathway. Predicted to act upstream of or within G protein-coupled receptor signaling pathway. Predicted to be located in Golgi apparatus and nuclear membrane. Predicted to be part of heterotrimeric G-protein complex. Predicted to be active in cytoplasm. Is expressed in several structures, including gonad; heart; immune system; liver; and nervous system. Human ortholog(s) of this gene implicated in Sturge-Weber syndrome; congestive heart failure; and familial multiple nevi flammei. Orthologous to human GNAQ (G protein subunit alpha q).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
7 figures from 5 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
ihb689Allele with one insertionExon 3UnknownCRISPR
sa17830Allele with one point mutationUnknownPremature StopENU
sa40565Allele with one point mutationUnknownSplice SiteENU
sa40566Allele with one point mutationUnknownPremature StopENU
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Sequence Targeting Reagents
Targeting Reagent Created Alleles Citations
CRISPR1-gnaqZebrafish Nomenclature Committee
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Human Disease
Associated With gnaq Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
familial multiple nevi flammei Alliance Capillary malformations, congenital, 1, somatic, mosaic 163000
Sturge-Weber syndrome Alliance Sturge-Weber syndrome, somatic, mosaic 185300
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Associated With gnaq Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Family IPR000654 G-protein alpha subunit, group Q
Family IPR001019 Guanine nucleotide binding protein (G-protein), alpha subunit
Homologous_superfamily IPR011025 G protein alpha subunit, helical insertion
Homologous_superfamily IPR027417 P-loop containing nucleoside triphosphate hydrolase
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Domain Details Per Protein
Protein Additional Resources Length G-protein alpha subunit, group Q G protein alpha subunit, helical insertion Guanine nucleotide binding protein (G-protein), alpha subunit P-loop containing nucleoside triphosphate hydrolase
UniProtKB:B8JLJ7 InterPro 359
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 5
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA gnaq-201 (1) Ensembl 1,745 nt
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Interactions and Pathways
No data available
Antibodies
Name Type Antigen Genes Isotype Host Organism Assay Source Citations
Ab1-gnaq Rabbit
  • IHC
ABclonal
1
1 - 1 of 1
Plasmids
No data available
Constructs
Construct Regulatory Region Coding Sequence Species Tg Lines Citations
Tg(cryaa:Venus,mitfa:gnaq_Q209P)
  • Danio rerio
3Mouti et al., 2016
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Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations
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