UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
thyroid gland development | ||
brain development | ||
glutathione metabolic process | ||
ion transport |
|
|
L-cystine transport |
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:0000488 | Retinopathy |
HP:0000495 | Recurrent corneal erosions |
HP:0000505 | Visual impairment |
HP:0000531 | Corneal crystals |
HP:0000580 | Pigmentary retinopathy |
HP:0000613 | Photophobia |
HP:0000618 | Blindness |
HP:0000787 | Nephrolithiasis |
HP:0000790 | Hematuria |
HP:0000819 | Diabetes mellitus |
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 |
---|---|---|---|
107553535 | SINGR64179 | ||
107597154 | SINGR49394 | ||
106825663 | EQUAS23655 | ||
116827837 | CHEAB18546 | ||
115042336 | ECHNA36178 | ||
113487275 | ATHCN17413 | ||
105817006 | PROCO25775 | ||
850438 | SGD:S000000671 | ||
109054775 | CYPCA125169 | ||
109065208 | CYPCA119345 |
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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