UniProt | Protein Name |
---|---|
Q14055 |
|
GO Term | Evidence Code | PMID |
---|---|---|
skeletal system development |
|
|
extracellular matrix organization |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum lumen |
|
|
extracellular region |
|
|
collagen-containing extracellular matrix | ||
extracellular space | ||
collagen type IX trimer |
GO Term | Evidence Code | PMID |
---|---|---|
protein homodimerization activity | ||
protein binding | ||
extracellular matrix structural constituent conferring tensile strength |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:1029 | familial periodic paralysis | |
DOID:10375 | strabismic amblyopia | |
DOID:10376 | amblyopia | |
DOID:10763 | hypertension | |
DOID:10825 | essential hypertension | |
DOID:1099 | alpha thalassemia | |
DOID:1115 | sarcoma | |
DOID:114 | heart disease | |
DOID:11504 | autonomic neuropathy | |
DOID:11782 | astigmatism |
HPO ID | HPO Term |
---|---|
HP:0002656 | Epiphyseal dysplasia |
HP:0002758 | Osteoarthritis |
HP:0002812 | Coxa vara |
HP:0002815 | Abnormality of the knee |
HP:0002857 | Genu valgum |
HP:0002970 | Genu varum |
HP:0003028 | Abnormality of the ankle |
HP:0003045 | Abnormal patella morphology |
HP:0003071 | Flattened epiphysis |
HP:0003198 | Myopathy |
Disease ID | Disease Name |
---|---|
OMIM:600204 |
|
ORPHA:250984 |
|
ORPHA:166002 |
|
OMIM:614284 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
100405504 | CALJA40137 | ||
105594700 | CERAT05852 | ||
102123592 | MACFA22715 | ||
694248 | MACMU21663 | ||
105494804 | MACNE01998 | ||
101007358 | PAPAN19548 | ||
105537944 | MANLE20398 | ||
101125128 | GORGO17552 | ||
100970548 | PANPA01077 | ||
456791 | PANTR20760 |
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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024