UniProt | Protein Name |
---|---|
O75787 |
|
GO Term | Evidence Code | PMID |
---|---|---|
intracellular pH reduction |
|
|
regulation of MAPK cascade | ||
eye pigmentation | ||
lysosomal lumen acidification | ||
positive regulation of transforming growth factor beta1 production |
GO Term | Evidence Code | PMID |
---|---|---|
extracellular exosome | ||
Golgi membrane |
|
|
endosome membrane | ||
lysosome | ||
tertiary granule membrane |
|
GO Term | Evidence Code | PMID |
---|---|---|
signaling receptor activity | ||
protein binding |
DO ID | Disease Name | Source |
---|---|---|
DOID:5844 | myocardial infarction | |
DOID:5854 | silent myocardial infarction | |
DOID:6000 | congestive heart failure | |
DOID:657 | adenoma | |
DOID:6688 | autoimmune lymphoproliferative syndrome | |
DOID:6713 | cerebrovascular disease | |
DOID:684 | hepatocellular carcinoma | |
DOID:784 | chronic kidney disease | |
DOID:7997 | thyrotoxicosis | |
DOID:7998 | hyperthyroidism |
HPO ID | HPO Term |
---|---|
HP:0000047 | Hypospadias |
HP:0000298 | Mask-like facies |
HP:0000338 | Hypomimic face |
HP:0000341 | Narrow forehead |
HP:0000347 | Micrognathia |
HP:0000369 | Low-set ears |
HP:0000750 | Delayed speech and language development |
HP:0000952 | Jaundice |
HP:0000973 | Cutis laxa |
HP:0001249 | Intellectual disability |
Disease ID | Disease Name |
---|---|
ORPHA:363654 |
|
OMIM:300911 |
|
OMIM:301045 |
|
OMIM:300423 |
|
ORPHA:93952 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
174109 | WB:WBGene00020500 | ||
181526 | WB:WBGene00010993 | ||
41104 | FB:FBgn0037671 | ||
103183828 | CALMI03163 | ||
102360219 | LATCH14143 | ||
406296 | ZFIN:ZDB-GENE-040426-1960 | DANRE22794 | |
103046401 | ASTMX10533 | ||
108259516 | ICTPU22329 | ||
100195062 | SALSA77940 | ||
115156323 | SALTR09087 |
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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