1. Gene
  2. SLC16A5 - solute carrier family 16 member 5 Gene

SLC16A5 - solute carrier family 16 member 5 Gene

Homo sapiens

Also known as MCT5; MCT6

Gene ID: 9121 | Gene type: protein coding

About SLC16A5

Cytogenetic location: 17q25.1 Genomic coordinates (GRCh38): 17:75,087,385-75,110,149 (from NCBI)

This gene has 10 transcripts (splice variants), 269 orthologues and 13 paralogues. Broad expression in lung (RPKM 9.8), duodenum (RPKM 9.3) and 21 other tissues.

Summary

This gene encodes a member of the Monocarboxylate Transporter family and the major facilitator superfamily. The encoded protein is localized to the cell membrane and acts as a proton-linked transporter of bumetanide. Transport by the encoded protein is inhibited by four loop diuretics, nateglinide, thiazides, probenecid, and glibenclamide. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Nov 2012]

SLC16A5 Products(3)

mRNA Protein Name
NM_001271765.2 NP_001258694.1 monocarboxylate transporter 6
NM_001369668.1 NP_001356597.1 monocarboxylate transporter 6
NM_004695.4 NP_004686.1 monocarboxylate transporter 6

SLC16A5 Protein Structure

MFS_1

MFS_1: Major Facilitator Superfamily (32 - 297)

  • 0
  • 100
  • 200
  • 300
  • 400
  • 505 a.a.
Protein Preferred Names Protein Names

monocarboxylate transporter 6

monocarboxylate transporter 5

Related Diseases

Diseases Alias
Allan-Herndon-Dudley Syndrome

AHDS

Allan-Herndon Syndrome

Monocarboxylate Transporter 8 Deficiency

MCT8 DEFICIENCY

Mental Retardation, X-Linked, With Hypotonia

Triiodothyronine Resistance

T3 Resistance

Mental Retardation And Muscular Atrophy

Mct8-Specific Thyroid Hormone Cell-Membrane Transporter Deficiency

Intellectual Disability And Muscular Atrophy

Monocarboxylate Transporter-8 Deficiency

T3 Resisitence

Triiodothyronine Resistence

X-Linked Intellectual Disability With Hypotonia

Mct8 -Specific Thyroid Hormone Cell Transporter Deficiency

Monocarboxylate Transporter 8 Deficiency

X-Linked Intellectual Disability-Hypotonia Syndrome

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
Mus musculus SLC16A5 MGD MGI:2443515
Macaca mulatta SLC16A5 VGNC VGNC:99257
Rattus norvegicus SLC16A5 RGD RGD:1582896
Bos taurus SLC16A5 VGNC VGNC:34691
Felis catus SLC16A5 VGNC VGNC:65212