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
Expression
All Expression Data
No data available
Cross-Species Comparison
High Throughput Data
Thisse Expression Data
No data available
Wild Type Expression Summary
Phenotype
All Phenotype Data
No data available
Cross-Species Comparison
Alliance
Phenotype Summary
Mutations
Mutants
Sequence Targeting Reagents
Human Disease
Associated With slc35a1 Human Ortholog
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
Associated With slc35a1 Via Experimental Models
No data available
Gene Ontology
Protein Domains
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
Transcripts
Genome Browsers
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
Antibodies
No data available
Plasmids
No data available
Constructs
Marker Relationships
Sequences
Orthology
Comparative Orthology
Alliance
Gene Tree
Ensembl
Citations