UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
brush border assembly | ||
adult walking behavior | ||
renal albumin absorption | ||
regulation of melanin biosynthetic process | ||
regulation of TORC1 signaling |
GO Term | Evidence Code | PMID |
---|---|---|
intracellular membrane-bounded organelle | ||
melanosome | ||
plasma membrane | ||
lysosomal membrane | ||
early endosome |
DO ID | Disease Name | Source |
---|---|---|
DOID:10141 | obsolete asthenopia | |
DOID:10573 | osteomalacia | |
DOID:10584 | retinitis pigmentosa | |
DOID:10609 | rickets | |
DOID:1062 | Fanconi syndrome | |
DOID:1064 | cystinosis | |
DOID:10652 | Alzheimer's disease | |
DOID:1074 | kidney failure | |
DOID:10787 | premature menopause | |
DOID:10952 | nephritis |
HPO ID | HPO Term |
---|---|
HP:0011462 | Young adult onset |
HP:0011968 | Feeding difficulties |
HP:0012408 | Medullary nephrocalcinosis |
HP:0012598 | Abnormal urine potassium concentration |
HP:0012622 | Chronic kidney disease |
HP:0100511 | Abnormality of vitamin D metabolism |
HP:0100512 | Decreased circulating vitamin D concentration |
HP:0100543 | Cognitive impairment |
HP:0200026 | Ocular pain |
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