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solute carrier family 35 member A2
Summary
- Gene Symbol
-
- SLC35A2
- Aliases
-
- UDP-Gal-Tr
- UDP-galactose translocator
- UGAT
- UGT
- UGT1
- UGT2
- UGTL
- Organism
- Homo sapiens (human)
Annotation
- Keyword
-
- Alternative splicing
- Antiport
- Congenital disorder of glycosylation
- Disease variant
- Endoplasmic reticulum
- Epilepsy
- Golgi apparatus
- Proteomics identification
- Reference proteome
- Sugar transport
- Transmembrane helix
- Proteins
Gene Ontology (GO)
| GO Term | Evidence Code | PMID |
|---|---|---|
| galactose metabolic process | ||
| UDP-galactose transmembrane transport |
| GO Term | Evidence Code | PMID |
|---|---|---|
| endoplasmic reticulum | ||
| endoplasmic reticulum membrane | ||
| Golgi apparatus | ||
| Golgi membrane | ||
| nucleoplasm |
GO Hierarchy
| GO Term | Evidence Code | PMID |
|---|---|---|
| antiporter activity | ||
| UDP-galactose transmembrane transporter activity | ||
| protein binding | ||
| sialic acid transmembrane transporter activity |
|
GO Hierarchy
Human Protein Atlas
Tissue with high expression from Human Protein Atlas. Tissues that are highly expressed are highlighted.
GlycoGene Database (GGDB)
- GGDB ID
- gg176
- Gene Symbol
-
- SLC35A2
- Orthologous Gene
| Species | Protein | mRNA |
|---|---|---|
| Drosophila melanogaster | NP_570019 | NM_130663 |
| Mus musculus | NP_511039 | NM_078484 |
KEGG BRITE Database
Disease
- Disease Ontology
| DO ID | Disease Name | Source |
|---|---|---|
| DOID:0060058 | lymphoma | |
| DOID:0060249 | scoliosis | |
| DOID:0060262 | gallbladder disease | |
| DOID:0060823 | syndromic X-linked intellectual disability 94 | |
| DOID:0050562 | West syndrome | |
| DOID:0050570 | congenital disorder of glycosylation type I | |
| DOID:0050571 | congenital disorder of glycosylation type II | |
| DOID:0050590 | severe congenital neutropenia | |
| DOID:0050639 | primary cutaneous amyloidosis | |
| DOID:0050848 | obstructive sleep apnea |
- The Human Phenotype Ontology
| HPO ID | HPO Term |
|---|---|
| HP:0000074 | Ureteropelvic junction obstruction |
| HP:0000194 | Open mouth |
| HP:0000218 | High palate |
| HP:0000252 | Microcephaly |
| HP:0000280 | Coarse facial features |
| HP:0000286 | Epicanthus |
| HP:0000293 | Full cheeks |
| HP:0000303 | Mandibular prognathia |
| HP:0000322 | Short philtrum |
| HP:0000407 | Sensorineural hearing impairment |
| Disease ID | Disease Name |
|---|---|
| ORPHA:356961 |
|
| OMIM:300896 |
|
PubChem Disease
- GHR Health Conditions
- MedGen Diseases
- OMIM Phenotypes
- KEGG Diseases
Ortholog
| Species | Gene ID | Alliance of Genome Resources | Orthologous MAtrix |
|---|---|---|---|
| 187393 | WB:WBGene00005153 | ||
| 191452 | WB:WBGene00014139 | ||
| 31255 | FB:FBgn0024994 | ||
| 102355053 | LATCH09079 | ||
| 555288 | ZFIN:ZDB-GENE-030616-62 | DANRE43027 | |
| 103035724 | ASTMX04044 | ||
| 108265841 | ICTPU30260 | ||
| 106566496 | SALSA64114 | ||
| 115168571 | SALTR76422 | ||
| 101172226 | ORYLA20208 |
