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 131 - 140 of 344 in total
DO ID Disease Name Source
DOID:10348 blepharophimosis
DOID:1040 chronic lymphocytic leukemia
DOID:10588 adrenoleukodystrophy
DOID:10591 pre-eclampsia
DOID:1063 interstitial nephritis
DOID:10652 Alzheimer's disease
DOID:1074 kidney failure
DOID:10763 hypertension
DOID:10871 age related macular degeneration
DOID:10907 microcephaly
The Human Phenotype Ontology
Displaying entries 101 - 110 of 248 in total
HPO ID HPO Term
HP:0001374 Congenital hip dislocation
HP:0001376 Limitation of joint mobility
HP:0001385 Hip dysplasia
HP:0001387 Joint stiffness
HP:0001392 Abnormality of the liver
HP:0001397 Hepatic steatosis
HP:0001508 Failure to thrive
HP:0001513 Obesity
HP:0001522 Death in infancy
HP:0001537 Umbilical hernia
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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