Protein name: MCT12 Aliases: MOT12 Substrates: N/D Transport type: Orphan transporter Tissue and cellular expression: kidney, retina, lung testis Subcellular expression: N/D Disease: juvenile cataracts with microcornea and renal glucosuria Locus: 10q23.31 Sequence ID: NP_998771.3, NM_213606.3 Gene ID: 387700 Splice variants: several splice variants listed in ENSG00000152779

MOT12_HUMAN (UniProt)

Gene names: SLC16A12, MCT12
Protein names and data: MOT12_HUMAN, Full=Monocarboxylate transporter 12;Short=MCT 12, Full=Solute carrier family 16 member 12; Length: 486 a.a., Mass: 53075 Da,
fasta formatted sequence

Function: Proton-linked monocarboxylate transporter. Catalyzes the rapid transport across the plasma membrane of many monocarboxylates (By similarity)
Cellular location: Cell membrane; Multi-pass membrane protein (By similarity)
Tissue specificity: Most highly expressed in kidney, followed by retina, lung, and testis. Very weakly expressed in brain and liver. Also detected in lens

Database cross-references

UniProt: Q6ZSM3
NextBio: 101521
OMIM: 611910 612018
Ensembl: ENST00000341233
GeneCard: GC10M089430
PharmGenUCSF: SLC16A12
Guide to Pharmacology: SLC16A12 (999)
SLC16 family of monocarboxylate transporters (999)

HGNC: HGNC:23094

Genetic variants

See also Ensembl:ENST00000341233