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:12336 | male infertility | |
DOID:13316 | exocrine pancreatic insufficiency | |
DOID:13636 | Fanconi anemia | |
DOID:1425 | pyoureter | |
DOID:14330 | Parkinson's disease | |
DOID:1443 | cerebral degeneration | |
DOID:14525 | Reye syndrome | |
DOID:1837 | diabetic ketoacidosis | |
DOID:1924 | hypogonadism | |
DOID:2089 | obsolete constipation |
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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Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
GlyCosmos Portal v4.0.0
Last updated: August 19, 2024