GO Term | Evidence Code | PMID |
---|---|---|
biphenyl catabolic process | ||
animal organ regeneration | ||
response to lipopolysaccharide | ||
flavonoid glucuronidation | ||
bilirubin conjugation |
GO Term | Evidence Code | PMID |
---|---|---|
endoplasmic reticulum | ||
endoplasmic reticulum membrane | ||
plasma membrane | ||
endoplasmic reticulum chaperone complex | ||
perinuclear region of cytoplasm |
GO Term | Evidence Code | PMID |
---|---|---|
steroid binding | ||
protein homodimerization activity | ||
enzyme binding | ||
enzyme inhibitor activity | ||
retinoic acid binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:8692 | myeloid leukemia | |
DOID:8778 | Crohn's disease | |
DOID:9119 | acute myeloid leukemia | |
DOID:9256 | colorectal cancer | |
DOID:9266 | cystinuria | |
DOID:9351 | diabetes mellitus | |
DOID:9352 | type 2 diabetes mellitus | |
DOID:936 | brain disease | |
DOID:9360 | intrinsic asthma | |
DOID:9408 | acute myocardial infarction |
HPO ID | HPO Term |
---|---|
HP:0001392 | Abnormality of the liver |
HP:0001399 | Hepatic failure |
HP:0002354 | Memory impairment |
HP:0002910 | Elevated circulating hepatic transaminase concentration |
HP:0003265 | Neonatal hyperbilirubinemia |
HP:0003577 | Congenital onset |
HP:0003623 | Neonatal onset |
HP:0006579 | Prolonged neonatal jaundice |
HP:0008176 | Neonatal unconjugated hyperbilirubinemia |
HP:0008282 | Unconjugated hyperbilirubinemia |
Disease ID | Disease Name |
---|---|
ORPHA:79234 |
|
ORPHA:79235 |
|
OMIM:237900 |
|
OMIM:218800 |
|
OMIM:143500 |
|
OMIM:606785 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
109096697 | CYPCA51496 | ||
116446652 | CORMO24175 | ||
103258345 | CARSF21068 | ||
115608460 | STRHB03216 | ||
115608461 | STRHB03216 | ||
115608795 | STRHB03216 |
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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