heparan sulfate proteoglycan 2

Summary
Gene Symbol
  • HSPG2
Aliases
  • PRCAN
  • endorepellin
  • perlecan
  • perlecan proteoglycan
Organism
Homo sapiens (human)
External Links
NCBI Gene
3339
HGNC
5273
KEGG Gene ID
hsa:3339
PubChem
3339
Alliance of Genome Resources
Annotation
Keyword
  • 3D-structure
  • Angiogenesis
  • Basement membrane
  • Calcium
  • Direct protein sequencing
  • Disease variant
  • Disulfide bond
  • EGF-like domain
  • Heparan sulfate
  • Immunoglobulin domain
  • Laminin EGF-like domain
  • Metal-binding
  • Reference proteome
  • Repeat
  • Signal
Proteins
Displaying 1 entry
UniProt Protein Name
P98160
  • Perlecan
Gene Ontology (GO)
GO Hierarchy
KEGG BRITE Database
Orthology
K06255
Name
basement membrane-specific heparan sulfate proteoglycan core protein
References
Disease
Disease Ontology
Displaying entries 181 - 190 of 344 in total
DO ID Disease Name Source
DOID:13810 familial hypercholesterolemia
DOID:1386 abetalipoproteinemia
DOID:1387 hypolipoproteinemia
DOID:1388 Tangier disease
DOID:13884 sick sinus syndrome
DOID:1391 Norum disease
DOID:13994 cleidocranial dysplasia
DOID:14018 alcoholic liver cirrhosis
DOID:14115 toxic shock syndrome
DOID:14221 abdominal obesity-metabolic syndrome 1
The Human Phenotype Ontology
Displaying entries 51 - 60 of 248 in total
HPO ID HPO Term
HP:0000520 Proptosis
HP:0000534 Abnormal eyebrow morphology
HP:0000545 Myopia
HP:0000581 Blepharophimosis
HP:0000600 Abnormality of the pharynx
HP:0000639 Nystagmus
HP:0000643 Blepharospasm
HP:0000648 Optic atrophy
HP:0000689 Dental malocclusion
HP:0000708 Atypical behavior
Displaying all 5 entries
Disease ID Disease Name
ORPHA:1606
  • chromosome 1p36 deletion syndrome
ORPHA:800
  • Schwartz-Jampel syndrome
ORPHA:1865
  • Silverman-Handmaker type dyssegmental dysplasia
OMIM:255800
  • Schwartz-Jampel syndrome type 1
OMIM:224410
  • Silverman-Handmaker type dyssegmental dysplasia

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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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