Gene

ephb4a

ID
ZDB-GENE-990415-62
Name
eph receptor B4a
Symbol
ephb4a Nomenclature History
Previous Names
  • ephB4 (1)
  • ephB4a
  • cb646 (1)
  • rtk5
Type
protein_coding_gene
Location
Chr: 5 Mapping Details/Browsers
Description
Predicted to enable transmembrane receptor protein tyrosine kinase activity. Acts upstream of or within convergent extension; ephrin receptor signaling pathway; and vasculature development. Predicted to be located in membrane. Predicted to be part of receptor complex. Predicted to be active in plasma membrane. Is expressed in several structures, including axis; cardiovascular system; digestive system; nervous system; and neural tube. Used to study lymphatic system disease. Human ortholog(s) of this gene implicated in central conducting lymphatic anomaly. Orthologous to human EPHB4 (EPH receptor B4).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
40 figures from 32 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
8 figures from 5 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
hu3378Allele with one point mutationUnknownUnknownENU
hu3445Allele with one point mutationUnknownPremature StopENU
ihb537Allele with one delinsUnknownUnknownCRISPR
ihb538Allele with one deletionUnknownUnknownCRISPR
la015774TgTransgenic insertionUnknownUnknownDNA
la025269TgTransgenic insertionUnknownUnknownDNA
sa11431Allele with one point mutationUnknownPremature StopENU
sa13275Allele with one point mutationUnknownPremature StopENU
sa30869Allele with one point mutationUnknownPremature StopENU
sa33770Allele with one point mutationUnknownPremature StopENU
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Sequence Targeting Reagents
Human Disease
Associated With ephb4a Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
central conducting lymphatic anomaly Alliance Lymphatic malformation 7 617300
Capillary malformation-arteriovenous malformation 2 618196
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Associated With ephb4a Via Experimental Models
Gene Ontology
Protein Domains
Domain, Family, and Site Summary
Type InterPro ID Name
Active_site IPR008266 Tyrosine-protein kinase, active site
Binding_site IPR017441 Protein kinase, ATP binding site
Conserved_site IPR001426 Tyrosine-protein kinase, receptor class V, conserved site
Domain IPR000719 Protein kinase domain
Domain IPR001090 Ephrin receptor ligand binding domain
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Domain Details Per Protein
Protein Length EPH-B4, SAM domain Ephrin receptor ligand binding domain Ephrin receptor, transmembrane domain Ephrin receptor type-A /type-B Ephrin receptor tyrosine kinases Ephrin type-B receptor 4, ligand binding domain Fibronectin type III Fibronectin type III superfamily Galactose-binding-like domain superfamily Growth factor receptor cysteine-rich domain superfamily Immunoglobulin-like fold Protein kinase, ATP binding site Protein kinase domain Protein kinase-like domain superfamily Serine-threonine/tyrosine-protein kinase, catalytic domain Sterile alpha motif domain Sterile alpha motif/pointed domain superfamily Tyrosine-protein kinase, active site Tyrosine-protein kinase, catalytic domain Tyrosine-protein kinase, receptor class V, conserved site
UniProtKB:A0A8M9Q872 986
UniProtKB:O73875 987
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 5
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA ephb4a-201 (1) Ensembl 2,940 nt
mRNA ephb4a-202 (1) Ensembl 1,308 nt
mRNA ephb4a-203 (1) Ensembl 3,056 nt
mRNA ephb4a-204 (1) Ensembl 2,186 nt
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Interactions and Pathways
No data available
Antibodies
No data available
Plasmids
No data available
Constructs
Construct Regulatory Region Coding Sequence Species Tg Lines Citations
Tg(UAS:ephb4a_K662R,cryaa:Cerulean)
  • Danio rerio
1 (2)
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Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inFosmidCH1073-264G23ZFIN Curated Data
Contained inFosmidZFOS-1566H6ZFIN Curated Data
ContainsSTSunp162
EncodesESTcb646Thisse et al., 2001
EncodescDNAMGC:136748ZFIN Curated Data
EncodescDNAMGC:171234ZFIN Curated Data
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanEPHB47
Functional complementation (1)
Amino acid sequence comparison (1)
MouseEphb45
Amino acid sequence comparison (1)
Citations
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