UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
transmembrane transport |
|
|
visual learning | ||
positive regulation of TORC1 signaling | ||
melanin biosynthetic process | ||
negative regulation of apoptotic process |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular exosome | ||
melanosome membrane | ||
lysosome | ||
late endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:0014667 | disease of metabolism | |
DOID:0050336 | hypophosphatemia | |
DOID:0050572 | cone-rod dystrophy | |
DOID:0060891 | Parkinson's disease 19A | |
DOID:0060895 | Parkinson's disease 4 | |
DOID:0060896 | Parkinson's disease 23 | |
DOID:0080001 | bone disease | |
DOID:0080348 | Alzheimer's disease 1 | |
DOID:0110035 | Alzheimer's disease 2 | |
DOID:0110037 | Alzheimer's disease 5 |
HPO ID | HPO Term |
---|---|
HP:0002500 | Abnormal cerebral white matter morphology |
HP:0002514 | Cerebral calcification |
HP:0002748 | Rickets |
HP:0002750 | Delayed skeletal maturation |
HP:0002857 | Genu valgum |
HP:0002900 | Hypokalemia |
HP:0002901 | Hypocalcemia |
HP:0002902 | Hyponatremia |
HP:0002907 | Microscopic hematuria |
HP:0002909 | Generalized aminoaciduria |
Disease ID | Disease Name |
---|---|
OMIM:219800 |
|
ORPHA:411629 |
|
OMIM:219900 |
|
ORPHA:411641 |
|
ORPHA:411634 |
|
OMIM:219750 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103751983 | NANGA18770 | ||
116453853 | CORMO10208 | ||
103263073 | CARSF10074 | ||
115602072 | STRHB05306 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024