SLC47A1 - solute carrier family 47 member 1 Gene

Homo sapiens

Also known as MATE1

Gene ID: 55244 | Gene type: protein coding

About SLC47A1

Cytogenetic location: 17p11.2 Genomic coordinates (GRCh38): 17:19,533,854-19,579,034 (from NCBI)

This gene has 14 transcripts (splice variants), 280 orthologues and 1 paralogue. Biased expression in adrenal (RPKM 59.0), kidney (RPKM 50.0) and 6 other tissues.

Summary

This gene is located within the Smith-Magenis syndrome region on chromosome 17. It encodes a protein of unknown function. [provided by RefSeq, Jul 2008]

SLC47A1 Products(1)

mRNA	Protein	Name
NM_018242.3	NP_060712.2	multidrug and toxin extrusion protein 1

SLC47A1 Protein Structure

MatE

0
100
200
300
400
500
570 a.a.

Protein Preferred Names

Protein Names

multidrug and toxin extrusion protein 1

MATE-1

Related Diseases

Diseases

Alias

Smith-Magenis Syndrome

SMS	Chromosome 17p11.2 Deletion Syndrome
17p11.2 Microdeletion Syndrome	17p11.2 Monosomy
Chromosome 17p Deletion Syndrome	Del(17)
P11.2	17p- Syndrome
Deletion 17p Syndrome	Partial Monosomy 17p

Diseases	Alias
Waldenstroem'S Macroglobulinemia	Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma Waldenstroem'S Macroglobulinemia Waldenstroem'S Macroglobulinemia Macroglobulinemia Of Waldenstrom Lymphoplasmacytic Lymphoma With Igm Gammopathy Lymphoplasmacytic Lymphoma

Related Agents

Pre-clinical Phase

Bioactive Molecules (1)

Cat. No.	Product Name	Effect	Purity	Rare Diseases
HY-RS13263	SLC47A1 Human Pre-designed siRNA Set A		/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Rattus norvegicus	SLC47A1	RGD	RGD:1311123
Canis familiaris	SLC47A1	VGNC	VGNC:49819
Bos taurus	SLC47A1	VGNC	VGNC:34887
Felis catus	SLC47A1	VGNC	VGNC:99453
Macaca mulatta	SLC47A1	VGNC	VGNC:77774

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