Homo sapiens Protein: PRG4 | |||||||||||||||||||
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Summary | |||||||||||||||||||
InnateDB Protein | IDBP-389812.4 | ||||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||||
Gene Symbol | PRG4 | ||||||||||||||||||
Protein Name | proteoglycan 4 | ||||||||||||||||||
Synonyms | bG174L6.2; CACP; HAPO; JCAP; MSF; SZP; | ||||||||||||||||||
Species | Homo sapiens | ||||||||||||||||||
Ensembl Protein | ENSP00000399679 | ||||||||||||||||||
InnateDB Gene | IDBG-105398 (PRG4) | ||||||||||||||||||
Protein Structure |
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UniProt Annotation | |||||||||||||||||||
Function | Plays a role in boundary lubrication within articulating joints. Prevents protein deposition onto cartilage from synovial fluid by controlling adhesion-dependent synovial growth and inhibiting the adhesion of synovial cells to the cartilage surface.Isoform F plays a role as a growth factor acting on the primitive cells of both hematopoietic and endothelial cell lineages. | ||||||||||||||||||
Subcellular Localization | Secreted {ECO:0000269PubMed:14976050}. | ||||||||||||||||||
Disease Associations | Camptodactyly-arthropathy-coxa vara-pericarditis syndrome (CACP) [MIM:208250]: Autosomal recessive disorder. Individuals with CACP have normal appearing joints at birth but with advancing age develop joint failure associated with noninflammatory synoviocyte hyperplasia and subintimal fibrosis of the synovial capsule. {ECO:0000269PubMed:10545950}. Note=The disease is caused by mutations affecting the gene represented in this entry. | ||||||||||||||||||
Tissue Specificity | Highly expressed in synovial tissue, cartilage and liver and weakly in heart and lung. Isoform B is expressed in kidney, lung, liver, heart and brain. Isoform C and isoform D are widely expressed. {ECO:0000269PubMed:10545950, ECO:0000269PubMed:11124536}. | ||||||||||||||||||
Comments | |||||||||||||||||||
Interactions | |||||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 2 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Protein Structure and Domains | |||||||||||||||||||
PDB ID | |||||||||||||||||||
InterPro |
IPR000585
Hemopexin-like domain IPR001212 Somatomedin B domain IPR018487 Hemopexin-like repeats IPR020436 Somatomedin B, chordata |
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PFAM |
PF01033
PF00045 |
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PRINTS |
PR00022
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PIRSF | |||||||||||||||||||
SMART |
SM00201
SM00120 |
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TIGRFAMs | |||||||||||||||||||
Post-translational Modifications | |||||||||||||||||||
Modification | |||||||||||||||||||
Cross-References | |||||||||||||||||||
SwissProt | Q92954 | ||||||||||||||||||
PhosphoSite | PhosphoSite-Q92954 | ||||||||||||||||||
TrEMBL | B3KQ20 | ||||||||||||||||||
UniProt Splice Variant | |||||||||||||||||||
Entrez Gene | 10216 | ||||||||||||||||||
UniGene | Hs.647723 | ||||||||||||||||||
RefSeq | NP_005798 | ||||||||||||||||||
HUGO | HGNC:9364 | ||||||||||||||||||
OMIM | 604283 | ||||||||||||||||||
CCDS | CCDS1369 | ||||||||||||||||||
HPRD | |||||||||||||||||||
IMGT | |||||||||||||||||||
EMBL | AK057197 AK131434 AL133553 AY653037 AY653038 U70136 | ||||||||||||||||||
GenPept | AAB09089 AAT74745 AAT74746 BAD18580 BAG51882 CAC36090 | ||||||||||||||||||