Basement membrane-specific heparan sulfate proteoglycan core protein
| Position | Description | PubMed ID | GlyTouCan ID | Source |
|---|---|---|---|---|
| 28 |
|
|||
| 40 |
|
|||
| 42 | O-linked (GalNAc...) threonine | |||
| 49 |
|
|||
| 52 |
|
|
||
| 65 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
| 71 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
| 76 | O-linked (Xyl...) (heparan sulfate) serine |
|
||
| 89 | N-linked (GlcNAc...) asparagine |
|
||
| 210 |
|
|
| Pathway Name | Organism |
|---|---|
| A tetrasaccharide linker sequence is required for GAG synthesis | Homo sapiens |
| Amyloid fiber formation | Homo sapiens |
| Attachment and Entry | Homo sapiens |
| Defective B3GALT6 causes EDSP2 and SEMDJL1 | Homo sapiens |
| Defective B3GAT3 causes JDSSDHD | Homo sapiens |
| Defective B4GALT7 causes EDS, progeroid type | Homo sapiens |
| Defective EXT1 causes exostoses 1, TRPS2 and CHDS | Homo sapiens |
| Defective EXT2 causes exostoses 2 | Homo sapiens |
| Degradation of the extracellular matrix | Homo sapiens |
| ECM proteoglycans | Homo sapiens |
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0090005 | Schwartz-Jampel syndrome 1 | |
| DOID:0090032 | Silverman-Handmaker type dyssegmental dysplasia | |
| DOID:2256 | osteochondrodysplasia |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
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Last updated: December 8, 2025