1. Gene
  2. SLC41A3 - solute carrier family 41 member 3 Gene

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

SLC41A3 Protein Structure

MgtE

MgtE: Divalent cation transporter (106 - 240)

MgtE

MgtE: Divalent cation transporter (318 - 456)

  • 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

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