Gene

insrb

ID
ZDB-GENE-020503-4
Name
insulin receptor b
Symbol
insrb Nomenclature History
Previous Names
  • IRb (1)
  • sb:eu666
  • si:dkey-6n3.1
Type
protein_coding_gene
Location
Chr: 22 Mapping Details/Browsers
Description
Predicted to enable insulin receptor activity and insulin receptor substrate binding activity. Acts upstream of or within with a positive effect on glycolytic process. Acts upstream of or within chordate embryonic development; developmental growth; and sprouting angiogenesis. Predicted to be located in membrane. Predicted to be part of insulin receptor complex. Predicted to be active in axon and plasma membrane. Is expressed in several structures, including endoderm; fertilized egg; immature eye; liver; and pleuroperitoneal region. Human ortholog(s) of this gene implicated in Donohue syndrome; glucose metabolism disease (multiple); hepatocellular carcinoma; and reproductive organ cancer (multiple). Orthologous to human INSR (insulin receptor).
Genome Resources
Note
None
Comparative Information
Expression
All Expression Data
22 figures from 18 publications
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
Wild Type Expression Summary
Phenotype
All Phenotype Data
20 figures from 6 publications
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Allele Type Localization Consequence Mutagen Supplier
ihb358Allele with one deletionExon 1Frameshift, Premature StopTALEN
la014143TgTransgenic insertionUnknownUnknownDNA
la014144TgTransgenic insertionUnknownUnknownDNA
la028387TgTransgenic insertionUnknownUnknownDNA
la028388TgTransgenic insertionUnknownUnknownDNA
sa6697Allele with one point mutationUnknownPremature StopENU
sa16909Allele with one point mutationUnknownPremature StopENU
sa32383Allele with one point mutationUnknownPremature StopENU
xu0422GtTransgenic insertionUnknownUnknownDNA
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Sequence Targeting Reagents
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Human Disease
Associated With insrb Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
Donohue syndrome Alliance Donohue syndrome 246200
familial hyperinsulinemic hypoglycemia 5 Alliance Hyperinsulinemic hypoglycemia, familial, 5 609968
Diabetes mellitus, insulin-resistant, with acanthosis nigricans 610549
Rabson-Mendenhall syndrome 262190
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Associated With insrb Via Experimental Models
No data available
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 IPR002011 Tyrosine-protein kinase, receptor class II, conserved site
Domain IPR000494 Receptor L-domain
Domain IPR000719 Protein kinase domain
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Domain Details Per Protein
Protein Additional Resources Length Fibronectin type III Fibronectin type III superfamily Furin-like cysteine-rich domain Furin-like repeat Growth factor receptor cysteine-rich domain superfamily Immunoglobulin-like fold Insulin receptor, trans-membrane domain Protein kinase, ATP binding site Protein kinase domain Protein kinase-like domain superfamily Receptor L-domain Receptor L-domain superfamily Receptor Tyrosine Kinase Serine-threonine/tyrosine-protein kinase, catalytic domain Tyrosine-protein kinase, active site Tyrosine-protein kinase, catalytic domain Tyrosine-protein kinase, insulin-like receptor Tyrosine-protein kinase, receptor class II, conserved site
UniProtKB:Q1LVG4 InterPro 1348
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Transcripts
Genome Browsers
Genome Build: GRCz11Chromosome: 22
Type Name Annotation Method Has Havana Data Length (nt) Analysis
mRNA insrb-201 (1) Ensembl 5,644 nt
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Interactions and Pathways
Antibodies
No data available
Plasmids
No data available
Constructs
No data available
Marker Relationships
Relationship Marker Type Marker Accession Numbers Citations
Contained inBACDKEY-6N3ZFIN Curated Data
Contained inBACDKEY-38O13ZFIN Curated Data
EncodesESTeu666Thisse et al., 2005
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Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Species Symbol Chromosome Accession # Evidence
HumanINSR19
Amino acid sequence comparison (2)
Conserved genome location (synteny) (1)
MouseInsr8
Amino acid sequence comparison (1)
Conserved genome location (synteny) (1)
Citations
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