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 |
DO ID | Disease Name | Source |
---|---|---|
DOID:2600 | laryngeal carcinoma | |
DOID:2739 | Gilbert syndrome | |
DOID:409 | liver disease | |
DOID:2741 | bilirubin metabolic disorder | |
DOID:2747 | glycogen storage disease | |
DOID:2749 | glycogen storage disease Ia | |
DOID:2752 | glycogen storage disease II | |
DOID:2773 | contact dermatitis | |
DOID:2841 | asthma | |
DOID:2859 | hemoglobin C disease |
HPO ID | HPO Term |
---|---|
HP:0000007 | Autosomal recessive inheritance |
HP:0000365 | Hearing impairment |
HP:0000750 | Delayed speech and language development |
HP:0000952 | Jaundice |
HP:0001080 | Biliary tract abnormality |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001298 | Encephalopathy |
HP:0001337 | Tremor |
HP:0001343 | Kernicterus |
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 |
---|---|---|---|
42774 | FB:FBgn0039085 | ||
42775 | FB:FBgn0039086 | ||
53501 | FB:FBgn0040250 | ||
53502 | FB:FBgn0040251 | ||
53503 | FB:FBgn0040252 | ||
53506 | FB:FBgn0040255 | ||
53507 | FB:FBgn0040256 | ||
53508 | FB:FBgn0040257 | ||
53511 | FB:FBgn0040260 | ||
53512 | FB:FBgn0040261 |
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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