General Information of Drug Transporter (DTP) (ID: DTZOKFJ)

DTP Name Monocarboxylate transporter 12 (SLC16A12)
Gene Name SLC16A12
UniProt ID
Q6ZSM3 (MOT12_HUMAN)
VARIDT ID
DTD0103
3D Structure
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2D Sequence (FASTA)
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3D Structure (PDB)
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Synonyms CJMG; CRT2; CTRCT47; Creatine transporter 2; MCT 12; MCT12; SLC16A12; Solute carrier family 16 member 12
DTP Family Major Facilitator Superfamily (MFS)
Monocarboxylate Transporter (MCT) Family
Tissue Specificity Most highly expressed in kidney, followed byretina, lung, heart and testis. Very weakly expressed in brain andliver. Also detected in lens.
Sequence
MPSGSHWTANSSKIITWLLEQPGKEEKRKTMAKVNRARSTSPPDGGWGWMIVAGCFLVTI
CTRAVTRCISIFFVEFQTYFTQDYAQTAWIHSIVDCVTMLCAPLGSVVSNHLSCQVGIML
GGLLASTGLILSSFATSLKHLYLTLGVLTGLGFALCYSPAIAMVGKYFSRRKALAYGIAM
SGSGIGTFILAPVVQLLIEQFSWRGALLILGGFVLNLCVCGALMRPITLKEDHTTPEQNH
VCRTQKEDIKRVSPYSSLTKEWAQTCLCCCLQQEYSFLLMSDFVVLAVSVLFMAYGCSPL
FVYLVPYALSVGVSHQQAAFLMSILGVIDIIGNITFGWLTDRRCLKNYQYVCYLFAVGMD
GLCYLCLPMLQSLPLLVPFSCTFGYFDGAYVTLIPVVTTEIVGTTSLSSALGVVYFLHAV
PYLVSPPIAGRLVDTTGSYTAAFLLCGFSMIFSSVLLGFARLIKRMRKTQLQFIAKESDP
KLQLWTNGSVAYSVARELDQKHGEPVATAVPGYSLT
Function This transporter is proton-linked monocarboxylate transporter that mediates creatine transport across the plasma membrane.
Endogenous Substrate(s) Monocarboxylates
TCDB ID
2.A.1.13.14
Gene ID
387700

Molecular Interaction Atlas (MIA) of This DTP

Molecular Interaction Atlas (MIA) Jump to Detail Molecular Interaction Atlas of This DTP
1 Clinical Trial Drug(s) Transported by This DTP
Drug Name Drug ID Indication ICD 11 Highest Status REF
Creatine ALS-08 DMKD2BQ Motor neurone disease 8B60 Phase 3 [1]
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References

1 Mutation in the Monocarboxylate Transporter 12 Gene Affects Guanidinoacetate Excretion but Does Not Cause Glucosuria. J Am Soc Nephrol. 2016 May;27(5):1426-36.