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 enable sodium-dependent multivitamin transmembrane transporter activity. Predicted to be involved in biotin transport; pantothenate transmembrane transport; and sodium ion transport. Predicted to act upstream of or within transmembrane transport. Predicted to be located in 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