UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
amino acid metabolic process |
|
|
protein transport | ||
monoatomic ion transport |
|
|
long-term memory | ||
positive regulation of thyroid hormone generation |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early 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:0001969 | Abnormal tubulointerstitial morphology |
HP:0001994 | Renal Fanconi syndrome |
HP:0002007 | Frontal bossing |
HP:0002013 | Vomiting |
HP:0002015 | Dysphagia |
HP:0002019 | Constipation |
HP:0002059 | Cerebral atrophy |
HP:0002148 | Hypophosphatemia |
HP:0002240 | Hepatomegaly |
HP:0002344 | Progressive neurologic deterioration |
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 |
---|---|---|---|
100077692 | ORNAN09090 | ||
100409361 | CALJA35932 | ||
105583831 | CERAT17187 | ||
102140046 | MACFA12686 | ||
706721 | MACMU15740 | ||
105471941 | MACNE31784 | ||
101007516 | PAPAN14005 | ||
101149722 | GORGO13059 | ||
100995234 | PANPA16046 | ||
748043 | PANTR13254 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024