Gene

ednraa

ID
ZDB-GENE-010906-2
Name
endothelin receptor type Aa
Symbol
ednraa Nomenclature History
Previous Names
  • Ednra2 (1)
  • ednra
  • etID40953.1 (1)
  • parade (1)
  • pde
  • wu:fb75g12
Type
protein_coding_gene
Location
Chr: 1 Mapping Details/Browsers
Description
Predicted to enable endothelin receptor activity. Acts upstream of with a positive effect on developmental pigmentation. Acts upstream of or within cartilage development; regulation of proton transport; and social behavior. Predicted to be located in membrane. Predicted to be active in plasma membrane. Is expressed in several structures, including epithelium; forebrain; neural crest; pharyngeal arch; and vasculature. Human ortholog(s) of this gene implicated in hypertension (multiple); lung disease; mandibulofacial dysostosis with alopecia; migraine; and obstructive sleep apnea. Orthologous to human EDNRA (endothelin receptor type A).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
11 figures from 9 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
20 figures from 5 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
hu4140Allele with one point mutationExon 5Premature StopENU
sa1973Allele with one point mutationUnknownPremature StopENU
sa11317Allele with one point mutationUnknownPremature StopENU
sa13839Allele with one point mutationUnknownPremature StopENU
sa19531Allele with one point mutationUnknownSplice SiteENU
sa19532Allele with one point mutationUnknownPremature StopENU
sa32714Allele with one point mutationUnknownPremature StopENU
tj262unknownUnknownExon Loss of Exon 7, FrameshiftENU
tv212unknownUnknownExon Loss of Exon 6, FrameshiftENU
yzu4EtTransgenic insertionUnknownUnknownDNA
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Sequence Targeting Reagents
Targeting Reagent Created Alleles Citations
MO2-ednraaN/A (3)
MO3-ednraaN/AGuh et al., 2014
MO4-ednraaN/ACamargo-Sosa et al., 2019
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Human Disease
Associated With ednraa Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
mandibulofacial dysostosis with alopecia Alliance Mandibulofacial dysostosis with alopecia 616367
migraine Alliance {Migraine, resistance to} 157300
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Associated With ednraa Via Experimental Models
No data available
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Domain IPR017452 GPCR, rhodopsin-like, 7TM
Family IPR000276 G protein-coupled receptor, rhodopsin-like
Family IPR000499 Endothelin receptor family
Family IPR002175 Endothelin receptor A
Family IPR051193 G-protein coupled endothelin receptor
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Domain Details Per Protein
Protein Length Endothelin receptor A Endothelin receptor family GPCR, rhodopsin-like, 7TM G-protein coupled endothelin receptor G protein-coupled receptor, rhodopsin-like
UniProtKB:B3DLG5 422
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 1
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA ednraa-201 (1) Ensembl 2,665 nt
mRNA ednraa-203 (1) Ensembl 200 nt
mRNA ednraa-204 (1) Ensembl 1,656 nt
mRNA ednraa-205 (1) Ensembl 1,690 nt
mRNA ednraa-206 (1) Ensembl 1,436 nt
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Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACCH211-172J10ZFIN Curated Data
EncodesESTfb75g12
EncodescDNAMGC:172066ZFIN Curated Data
EncodescDNAMGC:193800ZFIN Curated Data
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanEDNRA4
Amino acid sequence comparison (2)
Conserved genome location (synteny) (1)
Functional complementation (1)
MouseEdnra8
Amino acid sequence comparison (2)
Conserved genome location (synteny) (1)
Citations
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