UniProt | Protein Name |
---|---|
P22413 |
|
GO Term | Evidence Code | PMID |
---|---|---|
nucleoside triphosphate catabolic process | ||
negative regulation of glycogen biosynthetic process | ||
negative regulation of cell growth | ||
melanocyte differentiation | ||
vesicle-mediated transport |
GO Term | Evidence Code | PMID |
---|---|---|
lysosomal membrane | ||
plasma membrane | ||
extracellular space | ||
basolateral plasma membrane | ||
membrane |
GO Term | Evidence Code | PMID |
---|---|---|
scavenger receptor activity | ||
phosphodiesterase I activity | ||
3',5'-cyclic-AMP phosphodiesterase activity | ||
ATP binding | ||
UTP diphosphatase activity |
Gene Ontology |
---|
nucleoside triphosphate diphosphatase activity |
InterPro |
---|
Alkaline-phosphatase-like, core domain superfamily |
Type I phosphodiesterase/nucleotide pyrophosphatase/phosphate transferase |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0050644 | arterial calcification of infancy | |
DOID:0060887 | ossification of the posterior longitudinal ligament of spine | |
DOID:0080333 | aortic valve disease 1 | |
DOID:10754 | otitis media | |
DOID:1123 | spondyloarthropathy | |
DOID:1214 | tympanosclerosis | |
DOID:1287 | cardiovascular system disease | |
DOID:2738 | pseudoxanthoma elasticum | |
DOID:3068 | glioblastoma | |
DOID:783 | end stage renal disease |
HPO ID | HPO Term |
---|---|
HP:0000006 | Autosomal dominant inheritance |
HP:0000007 | Autosomal recessive inheritance |
HP:0000117 | Renal phosphate wasting |
HP:0000121 | Nephrocalcinosis |
HP:0000164 | Abnormality of the dentition |
HP:0000218 | High palate |
HP:0000365 | Hearing impairment |
HP:0000381 | Stapes ankylosis |
HP:0000405 | Conductive hearing impairment |
HP:0000407 | Sensorineural hearing impairment |
Disease ID | Disease Name |
---|---|
OMIM:125853 |
|
OMIM:601665 |
|
ORPHA:289176 |
|
OMIM:208000 |
|
ORPHA:758 |
|
OMIM:613312 |
|
OMIM:615522 |
|
ORPHA:51608 |
|
Species | Gene ID | OrthoDB | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|---|
18605 | MGI:97370 | MOUSE02168 | ||
85496 | RGD:628825 | RATNO19316 | ||
179663 | WB:WBGene00007753 | |||
179665 | WB:WBGene00007755 | |||
463002 | 9598_0:001f7b | PANTR39075 | ||
562399 | ZFIN:ZDB-GENE-040724-172 | DANRE19528 | ||
615535 | BOVIN35783 | |||
710140 | MACMU33642 | |||
850391 | SGD:S000000621 | |||
856699 | SGD:S000000742 |
GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.
Supported by JST NBDC Grant Number JPMJND2204
Partly supported by NIH Common Fund Grant #1U01GM125267-01
This work is licensed under Creative Commons Attribution 4.0 International
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Last updated: February 17, 2025