UniProt | Protein Name |
---|---|
B4DH54 |
|
P32189 |
|
A0A8I5KXY7 |
|
GO Term | Evidence Code | PMID |
---|---|---|
triglyceride metabolic process | ||
triglyceride biosynthetic process | ||
phosphorylation | ||
glycerol catabolic process | ||
glycerol-3-phosphate biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
nucleus | ||
cytosol | ||
mitochondrial outer membrane | ||
mitochondrion | ||
extracellular exosome |
GO Term | Evidence Code | PMID |
---|---|---|
glycerol kinase activity | ||
metal ion binding | ||
ATP binding | ||
protein binding |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060874 | isolated growth hormone deficiency type IB | |
DOID:0050557 | congenital muscular dystrophy | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0050630 | Aland Island eye disease | |
DOID:0060255 | rippling muscle disease 2 | |
DOID:0060363 | glycerol kinase deficiency | |
DOID:0060427 | chromosome Xp21 deletion syndrome | |
DOID:0060870 | isolated growth hormone deficiency | |
DOID:0060872 | isolated growth hormone deficiency type II | |
DOID:0060873 | isolated growth hormone deficiency type IA |
HPO ID | HPO Term |
---|---|
HP:0000028 | Cryptorchidism |
HP:0000316 | Hypertelorism |
HP:0000369 | Low-set ears |
HP:0000486 | Strabismus |
HP:0000846 | Adrenal insufficiency |
HP:0000939 | Osteoporosis |
HP:0001249 | Intellectual disability |
HP:0001250 | Seizure |
HP:0001254 | Lethargy |
HP:0001259 | Coma |
Disease ID | Disease Name |
---|---|
OMIM:307030 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
173747 | WB:WBGene00020007 | ||
36282 | FB:FBgn0033673 | ||
38221 | FB:FBgn0035266 | ||
43913 | FB:FBgn0025592 | ||
102351316 | LATCH14312 | ||
100136866 | ZFIN:ZDB-GENE-080204-72 | ||
103032412 | ASTMX11896 | ||
108259045 | ICTPU21131 | ||
108266598 | ICTPU31421 | ||
113575342 | ELEEL16789 |
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GlyCosmos Portal v4.0.0
Last updated: August 19, 2024