Slc2a13 - solute carrier family 2 (facilitated glucose transporter), member 13 Gene

Mus musculus

Also known as Gm308; 6530403A04; A630029G22Rik

Gene ID: 239606 | Gene type: protein coding

About Slc2a13

Summary

Enables protease binding activity. Predicted to be involved in myo-inositol transport and positive regulation of amyloid-beta formation. Located in organelle membrane. Is expressed in several structures, including brain; jaw; and thoracic segment skeleton. Orthologous to human SLC2A13 (solute carrier family 2 member 13). [provided by Alliance of Genome Resources, Apr 2022]

Slc2a13 Products(1)

mRNA	Protein	Name
NM_001033633.3	NP_001028805.2	proton myo-inositol cotransporter

Gene Ontology

Molecular Function
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables protease binding	IPI IPI: Inferred from physical interaction	26094765	MGI

Cellular Component GO Annotation	Evidence	Reference	Source
NOT located in early endosome	IDA IDA: Inferred from direct assay	14749729	MGI
NOT located in lysosome	IDA IDA: Inferred from direct assay	14749729	MGI
located in organelle membrane	IDA IDA: Inferred from direct assay	14749729	MGI
NOT located in synaptic vesicle	IDA IDA: Inferred from direct assay	14749729	MGI

EXP: Inferred from Experiment IDA: Inferred from direct assay IPI: Inferred from physical interaction IMP: Inferred from mutant phenotype IGI: Inferred from genetic interaction IEP: Inferred from expression pattern

Protein Preferred Names

Protein Names

proton myo-inositol cotransporter

h(+)-myo-inositol cotransporter	h(+)-myo-inositol symporter
hmit	solute carrier family 2 member 13

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13162	SLC2A13 Human Pre-designed siRNA Set A	Pre-designed Set	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Homo sapiens	Slc2a13	NCBI	NCBI:114134

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