Gene

slc5a6b

ID

ZDB-GENE-050913-86

Name

solute carrier family 5 member 6

Symbol

slc5a6b Nomenclature History

Previous Names

slc5a6
wu:fa19f06
zgc:114067

Type

protein_coding_gene

Location

Chr: 17 Mapping Details/Browsers

Description

Predicted to have sodium-dependent multivitamin transmembrane transporter activity. Predicted to be involved in biotin transport and pantothenate transmembrane transport. Predicted to localize to integral component of membrane. Orthologous to human SLC5A6 (solute carrier family 5 member 6).

Genome Resources

Note

None

Comparative Information

Expression

All Expression Data

No data available

Cross-Species Comparison

High Throughput Data

GEO (1)

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

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 slc5a6b Human Ortholog

Disease Ontology Term	Multi-Species Data	OMIM Term	OMIM Phenotype ID
		Peripheral motor neuropathy, childhood-onset, biotin-responsive	619903
		Sodium-dependent multivitamin transporter deficiency	618973

Associated With slc5a6b Via Experimental Models

No data available

Gene Ontology

Protein Domains

Domain, Family, and Site Summary

Type	InterPro ID	Name
Conserved_site	IPR018212	Sodium/solute symporter, conserved site
Family	IPR001734	Sodium/solute symporter
Homologous_superfamily	IPR038377	Sodium/glucose symporter superfamily