Protein name: MCT9 Aliases: MOT9 Substrates: N/D Transport type: Orphan transporter Tissue and cellular expression: endometrium, testis, ovary, breast, brain, kidney, spleen adrenal, retina Subcellular expression: N/D Disease: N/D Locus: 10q21.1 Sequence ID: NP_919274.1, NM_194298.2 Gene ID: 220963 Splice variants: several splice variants listed in ENSG00000165449

MOT9_HUMAN (UniProt)

Gene names: SLC16A9, C10orf36, MCT9
Protein names and data: MOT9_HUMAN, Full=Monocarboxylate transporter 9;Short=MCT 9, Full=Solute carrier family 16 member 9; Length: 509 a.a., Mass: 55794 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)

Database cross-references

UniProt: Q7RTY1
NextBio: 91108
Ensembl: ENST00000395348
GeneCard: GC10M059650
PharmGenUCSF: SLC16A9
Guide to Pharmacology: SLC16A9 (997)
SLC16 family of monocarboxylate transporters (997)

HGNC: HGNC:23520

Genetic variants

See also Ensembl:ENST00000395348