Gene

slc5a6a

ID

ZDB-GENE-041001-177

Name

solute carrier family 5 member 6a

Symbol

slc5a6a Nomenclature History

Previous Names

si:dkey-5g7.3 (1)
zgc:114092

Type

protein_coding_gene

Location

Chr: 20 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

Expression Atlas

UO scRNA-seq (UCSC browser)

Single Cell Expression Atlas

Daniocell

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 slc5a6a 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 slc5a6a 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
Family	IPR051163	Sodium:Solute Symporter (SSF)
Homologous_superfamily	IPR038377	Sodium/glucose symporter superfamily