GO Term | Evidence Code | PMID |
---|---|---|
response to xenobiotic stimulus | ||
cardiolipin acyl-chain remodeling | ||
fatty acid beta-oxidation | ||
response to insulin |
GO Term | Evidence Code | PMID |
---|---|---|
mitochondrial inner membrane | ||
mitochondrion | ||
mitochondrial nucleoid | ||
mitochondrial fatty acid beta-oxidation multienzyme complex |
GO Term | Evidence Code | PMID |
---|---|---|
fatty-acyl-CoA binding | ||
3-hydroxyacyl-CoA dehydratase activity | ||
long-chain-3-hydroxyacyl-CoA dehydrogenase activity | ||
enoyl-CoA hydratase activity | ||
acetyl-CoA C-acetyltransferase activity |
|
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050120 | hemophagocytic lymphohistiocytosis | |
DOID:0050476 | Barth syndrome | |
DOID:0050534 | congenital stationary night blindness | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050589 | inflammatory bowel disease | |
DOID:0050700 | cardiomyopathy | |
DOID:0050766 | choreaacanthocytosis | |
DOID:0050811 | congenital adrenal hyperplasia | |
DOID:0060235 | carnitine palmitoyltransferase II deficiency |
HPO ID | HPO Term |
---|---|
HP:0000662 | Nyctalopia |
HP:0000829 | Hypoparathyroidism |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001252 | Hypotonia |
HP:0001254 | Lethargy |
HP:0001259 | Coma |
HP:0001263 | Global developmental delay |
HP:0001270 | Motor delay |
HP:0001284 | Areflexia |
Disease ID | Disease Name |
---|---|
OMIM:609016 |
|
ORPHA:5 |
|
OMIM:609015 |
|
ORPHA:746 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
172310 | WB:WBGene00020347 | ||
180037 | WB:WBGene00001150 | ||
34276 | FB:FBgn0028479 | ||
100181980 | CIOIN00171 | ||
103183149 | CALMI26665 | ||
793834 | ZFIN:ZDB-GENE-041111-204 | DANRE12642 | |
553401 | ZFIN:ZDB-GENE-031222-5 | ||
103035446 | ASTMX07578 | ||
100304971 | ICTPU35343 | ||
118242359 | ELEEL37906 |
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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