Gene
slc35a1
- ID
- ZDB-GENE-080716-17
- Name
- solute carrier family 35 member A1
- Symbol
- slc35a1 Nomenclature History
- Previous Names
-
- wu:fl06g06
- zgc:194176
- zgc:194179
- Type
- protein_coding_gene
- Location
- Chr: 20 Mapping Details/Browsers
- Description
- Predicted to have UDP-galactose transmembrane transporter activity. Predicted to be involved in pyrimidine nucleotide-sugar transmembrane transport. Predicted to localize to integral component of Golgi membrane. Human ortholog(s) of this gene implicated in congenital disorder of glycosylation type IIf. Orthologous to human SLC35A1 (solute carrier family 35 member A1).
- Genome Resources
- Note
- None
- Comparative Information
- All Expression Data
- No data available
- Cross-Species Comparison
- High Throughput Data
- Thisse Expression Data
- No data available
Wild Type Expression Summary
- All Phenotype Data
- No data available
- Cross-Species Comparison
- Alliance
Phenotype Summary
Mutations
Human Disease
Disease Ontology Term | Multi-Species Data | OMIM Term | OMIM Phenotype ID |
---|---|---|---|
congenital disorder of glycosylation type IIf | Alliance | Congenital disorder of glycosylation, type IIf | 603585 |
Domain, Family, and Site Summary
Type | InterPro ID | Name |
---|---|---|
Family | IPR007271 | Nucleotide-sugar transporter |
Domain Details Per Protein
Protein | Length | Nucleotide-sugar transporter |
---|---|---|
UniProtKB:B3DIQ6
|
337 |
Type | Name | Annotation Method | Has Havana Data | Length (nt) | Analysis |
---|---|---|---|---|---|
mRNA |
slc35a1-201
(1)
|
Ensembl | 1,113 nt | ||
mRNA |
slc35a1-202
(1)
|
Ensembl | 670 nt |
Interactions and Pathways
No data available
Plasmids
No data available