GO Term | Evidence Code | PMID |
---|---|---|
negative regulation of cellular glucuronidation |
|
|
liver development | ||
negative regulation of steroid metabolic process | ||
cellular response to ethanol | ||
response to nutrient |
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:74 | hematopoietic system disease | |
DOID:7997 | thyrotoxicosis | |
DOID:7998 | hyperthyroidism | |
DOID:8543 | Hodgkin's lymphoma, lymphocytic-histiocytic predominance | |
DOID:8552 | chronic myeloid leukemia | |
DOID:8567 | Hodgkin's lymphoma | |
DOID:8577 | ulcerative colitis | |
DOID:8628 | Hodgkin's lymphoma, lymphocytic depletion | |
DOID:8651 | Hodgkin's granuloma | |
DOID:8654 | Hodgkin's lymphoma, mixed cellularity |
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 |
---|---|---|---|
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