UniProt | Protein Name |
---|---|
O60931 |
|
I3L4A9 |
|
A0A0S2Z3K3 |
|
A0A0S2Z3I9 |
|
GO Term | Evidence Code | PMID |
---|---|---|
renal glucose absorption | ||
proton transmembrane transport | ||
ATP metabolic process | ||
renal water absorption | ||
negative regulation of hydrogen peroxide biosynthetic process |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular exosome | ||
melanosome membrane | ||
lysosome | ||
late 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:0000007 | Autosomal recessive inheritance |
HP:0000026 | Male hypogonadism |
HP:0000083 | Renal insufficiency |
HP:0000093 | Proteinuria |
HP:0000103 | Polyuria |
HP:0000114 | Proximal tubulopathy |
HP:0000117 | Renal phosphate wasting |
HP:0000124 | Renal tubular dysfunction |
HP:0000479 | Abnormal retinal morphology |
HP:0000481 | Abnormal cornea morphology |
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 |
---|---|---|---|
100443212 | PONAB12322 | ||
100856090 | CANLF19189 | ||
112911435 | VULVU37655 | ||
123776992 | URSAM10038 | ||
100464695 | AILME03412 | ||
101670843 | MUSPF00573 | ||
101092308 | FELCA32631 | ||
122207295 | PANLE04243 | ||
101316505 | TURTR16210 | ||
118886526 | BALMU11293 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024