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Standards Ontologies Notations
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
Annotation information from UniProt.
Gene Ontology (GO)
Displaying entry 16 - 16 of 16 in total
GO Term Evidence Code PMID
cell differentiation
GO Hierarchy
Gene Ontology information from NCBI Gene and UniProt.
KEGG BRITE Database
Orthology
K06255
Name
basement membrane-specific heparan sulfate proteoglycan core protein
References
Disease
Disease Ontology
Displaying entries 271 - 280 of 344 in total
DO ID Disease Name Source
DOID:4001 ovarian carcinoma
DOID:4015 sarcomatoid carcinoma
DOID:417 autoimmune disease
DOID:418 systemic scleroderma
DOID:419 scleroderma
DOID:4195 hyperglycemia
DOID:4254 osteosclerosis
DOID:4411 hepatitis E
DOID:4448 macular degeneration
DOID:4480 achondroplasia
The Human Phenotype Ontology
Displaying entries 1 - 10 of 248 in total
HPO ID HPO Term
HP:0000007 Autosomal recessive inheritance
HP:0000023 Inguinal hernia
HP:0000028 Cryptorchidism
HP:0000047 Hypospadias
HP:0000055 Abnormal female external genitalia morphology
HP:0000069 Abnormality of the ureter
HP:0000077 Abnormality of the kidney
HP:0000079 Abnormality of the urinary system
HP:0000107 Renal cyst
HP:0000119 Abnormality of the genitourinary system
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
PubChem Disease
GHR Health Conditions
MedGen Diseases
OMIM Phenotypes
KEGG Diseases
Gene-Disease-Co-Occurrences-in-Literature (PubChem)
Ortholog
Displaying entries 21 - 30 of 58 in total
Species Gene ID Alliance of Genome Resources Orthologous MAtrix
403440 CANLF07063
100467831 AILME12467
101681560 MUSPF18500
101094520 FELCA19382
122226287 PANLE10175
118890557 BALMU22335
100071701 HORSE27583
100517288 PIGXX29237
444872 BOVIN25243
102188640 CAPHI19907
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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: August 19, 2024