insulin receptor

Summary
Gene Symbol
  • INSR
Aliases
  • CD220
Organism
Homo sapiens (human)
NCBI Gene
3643
HGNC
6091
PubChem
3643
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • ATP-binding
  • Alternative splicing
  • Carbohydrate metabolism
  • Cell membrane
  • Cleavage on pair of basic residues
  • Diabetes mellitus
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • Endosome
  • Glycoprotein
  • Lysosome
  • Phosphoprotein
  • Receptor
  • Reference proteome
  • Repeat
  • S-nitrosylation
  • Signal
  • Transmembrane helix
  • Tyrosine-protein kinase
Proteins
Displaying 1 entry
UniProt Protein Name
P06213
Gene Ontology (GO)
GO Hierarchy
Displaying entries 1 - 5 of 23 in total
GO Term Evidence Code PMID
nuclear envelope
lysosome
late endosome
plasma membrane
plasma membrane
GO Hierarchy
GO Hierarchy
Disease
Disease Ontology
Displaying all 7 entries
DO ID Disease Name Source
DOID:0050470 Donohue syndrome
DOID:0070220 familial hyperinsulinemic hypoglycemia 5
DOID:11714 gestational diabetes
DOID:2526 prostate adenocarcinoma
DOID:3594 choriocarcinoma
DOID:9351 diabetes mellitus
DOID:9352 type 2 diabetes mellitus
The Human Phenotype Ontology
Displaying entries 1 - 10 of 119 in total
HPO ID HPO Term
HP:0000006 Autosomal dominant inheritance
HP:0000007 Autosomal recessive inheritance
HP:0000040 Long penis
HP:0000065 Labial hypertrophy
HP:0000105 Enlarged kidney
HP:0000121 Nephrocalcinosis
HP:0000138 Ovarian cyst
HP:0000154 Wide mouth
HP:0000158 Macroglossia
HP:0000164 Abnormality of the dentition
Displaying all 7 entries
Disease ID Disease Name
ORPHA:2297
  • insulin-resistance syndrome type A
ORPHA:508
  • Donohue syndrome
OMIM:246200
  • Donohue syndrome
OMIM:262190
  • Rabson-Mendenhall syndrome
OMIM:609968
  • hyperinsulinism due to INSR deficiency
ORPHA:263458
  • hyperinsulinism due to INSR deficiency
ORPHA:769
  • Rabson-Mendenhall syndrome
ChIP-Atlas
Target Genes
Predicted target genes bound by given transcription factors. Target Genes
Potential target genes for INSR
Distance from TSS: ± 10 kb
Displaying entries 1 - 10 of 52 in total
Gene Symbol Description Cellline (score)
solute carrier family 35 member B4
  • Hep_G2(123)
  • Hep_G2(145)
  • Hep_G2(194)
  • SH-SY5Y(195)
mannose phosphate isomerase
  • Hep_G2(134)
  • Hep_G2(178)
  • Hep_G2(257)
sphingomyelin phosphodiesterase 3
  • Hep_G2(112)
  • Hep_G2(140)
  • Hep_G2(197)
  • Hep_G2(324)
  • SH-SY5Y(463)
phosphomannomutase 2
  • Hep_G2(157)
  • Hep_G2(74)
ADP-ribosylserine hydrolase
  • Hep_G2(88)
decapping mRNA 1A
  • Hep_G2(81)
  • Hep_G2(97)
  • SH-SY5Y(114)
fatty acid synthase
  • Hep_G2(120)
Rac family small GTPase 3
  • Hep_G2(121)
ectonucleotide pyrophosphatase/phosphodiesterase 3
  • Hep_G2(154)
  • Hep_G2(168)
  • Hep_G2(193)
  • Hep_G2(227)
  • SH-SY5Y(93)
ALG5 dolichyl-phosphate beta-glucosyltransferase
  • Hep_G2(112)
  • Hep_G2(130)
  • Hep_G2(76)
Colocalization
Predicted partner proteins colocalizing with given transcription factors. Colocalization
Colocalization analysis for INSR
Displaying all 6 entries
Gene Symbol Description Cellline (score)
decapping mRNA 1A
  • SH-EP(0)
structural maintenance of chromosomes flexible hinge domain containing 1
  • SH-SY5Y(0)
  • SH-SY5Y(4)
  • SH-SY5Y(9)
  • hTERT_RPE-1(0)
methyl-CpG binding domain 4, DNA glycosylase
  • Hep_G2(0)
insulin receptor
  • Hep_G2(10)
  • Hep_G2(9)
  • SH-SY5Y(10)
  • SH-SY5Y(9)
INO80 complex ATPase subunit
  • Hep_G2(0)
  • HuH-7(0)
histone deacetylase 2
  • Hep_G2(0)
  • U-87_MG(0)

About Release Notes Help Feedback

Click here to visit the beta site.


International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.2.1

Last updated: April 7, 2025