insulin receptor

Summary
Gene Symbol
  • INSR
Aliases
  • CD220
Organism
Homo sapiens (human)
NCBI Gene
3643
HGNC
6091
PubChem
3643
Alliance of Genome Resources
JoGo
INSR
TogoVar
INSR
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
  • Isopeptide bond
  • Lysosome
  • Phosphoprotein
  • Proteomics identification
  • Receptor
  • Reference proteome
  • Repeat
  • S-nitrosylation
  • Signal
  • Transmembrane helix
  • Tyrosine-protein kinase
  • Ubl conjugation
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
OMIM:609968
  • hyperinsulinism due to INSR deficiency
OMIM:246200
  • Donohue syndrome
ORPHA:2297
  • insulin-resistance syndrome type A
ORPHA:769
  • Rabson-Mendenhall syndrome
OMIM:262190
  • Rabson-Mendenhall syndrome
ORPHA:508
  • Donohue syndrome
ORPHA:263458
  • hyperinsulinism due to INSR deficiency
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)
hyaluronidase 3
  • Hep_G2(1140)
  • Hep_G2(715)
  • Hep_G2(894)
  • Hep_G2(926)
  • SH-SY5Y(214)
  • SH-SY5Y(409)
phosphatidylinositol glycan anchor biosynthesis class U
  • Hep_G2(128)
  • Hep_G2(219)
  • Hep_G2(97)
  • SH-SY5Y(81)
fatty acid synthase
  • Hep_G2(120)
inositol polyphosphate-5-phosphatase B
  • Hep_G2(103)
ectonucleotide pyrophosphatase/phosphodiesterase 3
  • Hep_G2(154)
  • Hep_G2(168)
  • Hep_G2(193)
  • Hep_G2(227)
  • SH-SY5Y(93)
solute carrier family 35 member A3
  • Hep_G2(157)
fucosyltransferase 1 (H blood group)
  • Hep_G2(139)
  • Hep_G2(225)
  • Hep_G2(237)
  • Hep_G2(372)
  • SH-SY5Y(181)
chondroitin polymerizing factor 2
  • Hep_G2(105)
  • Hep_G2(201)
  • Hep_G2(225)
  • Hep_G2(240)
  • SH-SY5Y(336)
RAB1A, member RAS oncogene family
  • Hep_G2(131)
  • Hep_G2(203)
  • Hep_G2(239)
  • Hep_G2(285)
  • SH-SY5Y(130)
ALG10 alpha-1,2-glucosyltransferase
  • Hep_G2(101)
Colocalization
Predicted partner proteins colocalizing with given transcription factors. Colocalization
Colocalization analysis for INSR
Displaying all 6 entries
Gene Symbol Description Cellline (score)
histone deacetylase 2
  • Hep_G2(0)
  • U-87_MG(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)
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)

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


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Last updated: April 6, 2026