UniProt | Protein Name |
---|---|
O95528 |
|
GO Term | Evidence Code | PMID |
---|---|---|
dehydroascorbic acid transport | ||
glucose transmembrane transport | ||
galactose transmembrane transport |
|
|
embryonic skeletal joint development | ||
cell redox homeostasis |
GO Term | Evidence Code | PMID |
---|---|---|
carbohydrate:proton symporter activity |
|
|
symporter activity | ||
D-glucose transmembrane transporter activity | ||
dehydroascorbic acid transmembrane transporter activity |
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
DO ID | Disease Name | Source |
---|---|---|
DOID:0060321 | umbilical hernia | |
DOID:0060327 | omphalocele | |
DOID:0060731 | congenital central hypoventilation syndrome | |
DOID:0060762 | restrictive dermopathy | |
DOID:0060862 | mal de Meleda | |
DOID:0070129 | autosomal recessive cutis laxa type IID | |
DOID:0070130 | autosomal dominant cutis laxa 1 | |
DOID:0070131 | autosomal dominant cutis laxa 3 | |
DOID:0070132 | autosomal recessive cutis laxa type IIIA | |
DOID:0070133 | autosomal recessive cutis laxa type IB |
HPO ID | HPO Term |
---|---|
HP:0001249 | Intellectual disability |
HP:0001252 | Hypotonia |
HP:0001263 | Global developmental delay |
HP:0001290 | Generalized hypotonia |
HP:0001328 | Specific learning disability |
HP:0001363 | Craniosynostosis |
HP:0001371 | Flexion contracture |
HP:0001382 | Joint hypermobility |
HP:0001385 | Hip dysplasia |
HP:0001537 | Umbilical hernia |
Disease ID | Disease Name |
---|---|
OMIM:208050 |
|
ORPHA:3342 |
|
Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
---|---|---|---|
103186264 | CALMI34221 | ||
102364983 | LATCH10365 | ||
560546 | ZFIN:ZDB-GENE-080204-6 | DANRE03179 | |
103042379 | ASTMX05310 | ||
108255251 | ICTPU16406 | ||
106565264 | SALSA24493 | ||
115208344 | SALTR34707 | ||
115542397 | GADMO27705 | ||
100710582 | ORENI59894 | ||
115583513 | SPAAU42212 |
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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