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 |
---|---|---|
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: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 |
---|---|---|---|
100669881 | LOXAF07846 | ||
100060554 | HORSE03110 | ||
100515235 | PIGXX03131 | ||
613527 | BOVIN12569 | ||
102187709 | CAPHI10245 | ||
101122533 | SHEEP02647 | ||
105983465 | DIPOR08657 | ||
83429 | MGI:1932872 | MOUSE07194 | |
287478 | RGD:1308466 | RATNO00724 | |
101721174 | HETGA14366 |
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Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024