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:4674 | androgen insensitivity syndrome | |
DOID:5003 | eunuchism | |
DOID:557 | kidney disease | |
DOID:5679 | retinal disease | |
DOID:5684 | spondyloepimetaphyseal dysplasia, Sponastrime type | |
DOID:576 | proteinuria | |
DOID:580 | uric acid nephrolithiasis | |
DOID:585 | nephrolithiasis | |
DOID:65 | connective tissue disease | |
DOID:9351 | diabetes mellitus |
HPO ID | HPO Term |
---|---|
HP:0001508 | Failure to thrive |
HP:0001510 | Growth delay |
HP:0001531 | Failure to thrive in infancy |
HP:0001738 | Exocrine pancreatic insufficiency |
HP:0001744 | Splenomegaly |
HP:0001824 | Weight loss |
HP:0001941 | Acidosis |
HP:0001942 | Metabolic acidosis |
HP:0001944 | Dehydration |
HP:0001959 | Polydipsia |
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 |
---|---|---|---|
174308 | WB:WBGene00008052 | ||
42723 | FB:FBgn0039045 | ||
100187335 | CIOIN10021 | ||
103183486 | CALMI27654 | ||
102362641 | LATCH17786 | ||
553594 | ZFIN:ZDB-GENE-050522-352 | DANRE02414 | |
103043999 | ASTMX02927 | ||
108271312 | ICTPU01685 | ||
113574465 | ELEEL14498 | ||
106613706 | SALSA10341 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024