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 |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:0110038 | Alzheimer's disease 6 | |
DOID:0110039 | Alzheimer's disease 7 | |
DOID:0110041 | Alzheimer's disease 8 | |
DOID:0110043 | Alzheimer's disease 10 | |
DOID:0110044 | Alzheimer's disease 11 | |
DOID:0110045 | Alzheimer's disease 12 | |
DOID:0110046 | Alzheimer's disease 13 | |
DOID:0110047 | Alzheimer's disease 14 | |
DOID:0110048 | Alzheimer's disease 15 | |
DOID:0110273 | autosomal dominant limb-girdle muscular dystrophy |
HPO ID | HPO Term |
---|---|
HP:0002917 | Hypomagnesemia |
HP:0002926 | Abnormality of thyroid physiology |
HP:0003016 | Metaphyseal widening |
HP:0003076 | Glycosuria |
HP:0003109 | Hyperphosphaturia |
HP:0003111 | Abnormal blood ion concentration |
HP:0003126 | Low-molecular-weight proteinuria |
HP:0003198 | Myopathy |
HP:0003202 | Skeletal muscle atrophy |
HP:0003234 | Decreased circulating carnitine concentration |
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