Gene

slc35a2

ID
ZDB-GENE-030616-62
Name
solute carrier family 35 member 2
Symbol
slc35a2 Nomenclature History
Previous Names
  • si:bz30i22.3
  • si:dkey-83k24.4
  • si:rp71-30i22.3
Type
protein_coding_gene
Location
Chr: 8 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 IIm. Orthologous to human SLC35A2 (solute carrier family 35 member A2).
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 slc35a2 Human Ortholog
Disease Ontology Term Multi-Species Data OMIM Term OMIM Phenotype ID
congenital disorder of glycosylation type IIm Alliance Congenital disorder of glycosylation, type IIm 300896
Associated With slc35a2 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:B0UYD3 374
UniProtKB:A0A8M2BEP2 379
Transcripts
Genome Browsers
Type Name Annotation Method Length (nt) Analysis
mRNA slc35a2-201 (1) Havana 1252 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