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 31 - 40 of 344 in total
DO ID Disease Name Source
DOID:0060583 Noonan syndrome 5
DOID:0060584 Noonan syndrome 6
DOID:0060585 Noonan syndrome 7
DOID:0060586 Noonan syndrome 8
DOID:0060587 Noonan syndrome 9
DOID:0060588 Noonan syndrome 10
DOID:0060608 microcephalic osteodysplastic primordial dwarfism type I
DOID:0060609 microcephalic osteodysplastic primordial dwarfism type II
DOID:0060644 chondrodysplasia-pseudohermaphroditism syndrome
DOID:0060673 Peters anomaly
The Human Phenotype Ontology
Displaying entries 71 - 80 of 248 in total
HPO ID HPO Term
HP:0000787 Nephrolithiasis
HP:0000821 Hypothyroidism
HP:0000878 11 pairs of ribs
HP:0000892 Bifid ribs
HP:0000902 Rib fusion
HP:0000912 Sprengel anomaly
HP:0000926 Platyspondyly
HP:0000939 Osteoporosis
HP:0000944 Abnormal metaphysis morphology
HP:0000946 Hypoplastic ilia
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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