SLC41A3 - solute carrier family 41 member 3 Gene

Homo sapiens

Also known as SLC41A1-L2

Gene ID: 54946 | Gene type: protein coding

About SLC41A3

Cytogenetic location: 3q21.2-q21.3 Genomic coordinates (GRCh38): 3:126,006,357-126,101,520 (from NCBI)

This gene has 22 transcripts (splice variants), 268 orthologues and 2 paralogues. Ubiquitous expression in testis (RPKM 23.3), ovary (RPKM 19.3) and 25 other tissues.

Summary

Predicted to enable cation transmembrane transporter activity. Predicted to be involved in cation transmembrane transport. Located in plasma membrane. [provided by Alliance of Genome Resources, Apr 2022]

SLC41A3 Products(5)

mRNA	Protein	Name
NM_001008485.2	NP_001008485.2	solute carrier family 41 member 3 isoform 1
NM_001008486.2	NP_001008486.2	solute carrier family 41 member 3 isoform 3
NM_001008487.2	NP_001008487.1	solute carrier family 41 member 3 isoform 4
NM_001164475.2	NP_001157947.1	solute carrier family 41 member 3 isoform 5
NM_017836.4	NP_060306.4	solute carrier family 41 member 3 isoform 2

Gene Ontology

Molecular Function
Biological Process
Cellular Component

Molecular Function GO Annotation	Evidence	Reference	Source
enables magnesium:sodium antiporter activity	IDA IDA: Inferred from direct assay	27302215	GOA
enables protein binding	IPI IPI: Inferred from physical interaction	25416956	GOA

Biological Process GO Annotation	Evidence	Reference	Source
involved in mitochondrial magnesium ion transmembrane transport	IDA IDA: Inferred from direct assay	27302215	GOA

Cellular Component GO Annotation	Evidence	Reference	Source
located in mitochondrial inner membrane	IDA IDA: Inferred from direct assay	27302215	GOA

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

SLC41A3 Protein Structure

MgtE

0
100
200
300
400
507 a.a.

Protein Preferred Names

Protein Names

solute carrier family 41 member 3

SLC41A1-like 2

Related Diseases

Diseases

Alias

Hypomagnesemia 1, Intestinal

Intestinal Hypomagnesemia 1	HOMG1
Hypomagnesemia With Secondary Hypocalcemia	Hsh
Hypomagnesemic Tetany	Intestinal Hypomagnesemia With Secondary Hypocalcemia
Homg	Hypomagnesemia Caused By Selective Magnesium Malabsorption
Hypomagnesemia Intestinal Type 1	Primary Hypomagnesemia With Secondary Hypocalcemia
Phsh	Hypomagnesemia, Intestinal, With Secondary Hypocalcemia
Familial Primary Hypomagnesemia With Hypocalcuria	Hypomagnesemia 1
Hypomagnesmic Tetany

Primary Hypomagnesemia

Familial Primary Hypomagnesemia	Homg
Primary Familial Hypomagnesemia	Genetic Primary Hypomagnesemia
Hypomagnesemia 1, Intestinal

Nephronophthisis

Medullary Cystic Disease	Medullary Cystic Kidney
Nph	Nphp
Kidney Disease, Cystic, Medullary

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-RS13247	SLC41A3 Human Pre-designed siRNA Set A	Pre-designed Sets	/	Unkown

Orthologs Information

Species	Symbol	Source	ID
Canis familiaris	SLC41A3	VGNC	VGNC:46414
Bos taurus	SLC41A3	VGNC	VGNC:58412
Rattus norvegicus	SLC41A3	RGD	RGD:1589573
Mus musculus	SLC41A3	MGD	MGI:1918949
Macaca mulatta	SLC41A3	VGNC	VGNC:77586

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