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: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:0000488 | Retinopathy |
HP:0000495 | Recurrent corneal erosions |
HP:0000505 | Visual impairment |
HP:0000531 | Corneal crystals |
HP:0000580 | Pigmentary retinopathy |
HP:0000613 | Photophobia |
HP:0000618 | Blindness |
HP:0000787 | Nephrolithiasis |
HP:0000790 | Hematuria |
HP:0000819 | Diabetes mellitus |
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 |
---|---|---|---|
101877876 | MELUD16955 | ||
102446187 | PELSI17857 | ||
103667133 | URSMA14009 | ||
114033319 | VOMUR22067 | ||
113878458 | BOBOX13941 | ||
100965339 | OTOGA04189 | ||
102021112 | CHILA16350 | ||
105714400 | AOTNA32080 | ||
110193155 | PHACI12809 | ||
101035490 | SAIBB21605 |
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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