Gene

slc1a3b

ID

ZDB-GENE-090708-3

Name

solute carrier family 1 member 3b

Symbol

slc1a3b Nomenclature History

Previous Names

EAAT1B (1)
glastb (1)
si:dkey-21n12.2

Type

protein_coding_gene

Location

Chr: 10 Mapping Details/Browsers

Description

Predicted to have symporter activity. Predicted to localize to integral component of membrane. Is expressed in nervous system. Human ortholog(s) of this gene implicated in episodic ataxia type 6. Orthologous to human SLC1A3 (solute carrier family 1 member 3).

Genome Resources

Note

None

Expression

All Expression Data

4 figures from 4 publications

Cross-Species Comparison

High Throughput Data

No data available

Thisse Expression Data

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 slc1a3b Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
episodic ataxia type 6	Alliance	Episodic ataxia, type 6	612656

Associated With slc1a3b Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Conserved_site	IPR018107	Sodium:dicarboxylate symporter, conserved site
Family	IPR001991	Sodium:dicarboxylate symporter
Homologous_superfamily	IPR036458	Sodium:dicarboxylate symporter superfamily