Gene
Entrez ID Entrez Gene ID - the GENE ID in NCBI Gene database.
220963
Gene name Gene Name - the full gene name approved by the HGNC.
Solute carrier family 16 member 9
Gene symbol Gene Symbol - the official gene symbol approved by the HGNC.
SLC16A9
Synonyms (NCBI Gene) Gene synonyms aliases
C10orf36, MCT9
Chromosome Chromosome number
10
Chromosome location Chromosomal Location - indicates the cytogenetic location of the gene or region on the chromosome.
10q21.2
miRNA miRNA information provided by mirtarbase database.
miRTarBase ID miRNA Experiments Reference
MIRT002800 hsa-miR-1-3p Microarray 15685193
MIRT002800 hsa-miR-1-3p Microarray 15685193
MIRT002800 hsa-miR-1-3p Microarray 18668037
MIRT044874 hsa-miR-194-5p CLASH 23622248
MIRT043968 hsa-miR-378a-5p CLASH 23622248
Gene ontology (GO) Gene ontology information of associated ontologies with gene provided by GO database.
GO ID Ontology Definition Evidence Reference
GO:0005515 Function Protein binding IPI 25416956
GO:0005887 Component Integral component of plasma membrane IBA 21873635
GO:0008028 Function Monocarboxylic acid transmembrane transporter activity IBA 21873635
GO:0015293 Function Symporter activity IEA
GO:0015718 Process Monocarboxylic acid transport IBA 21873635
Other IDs Other ids provides unique ids of gene in databases such as OMIM, HGNC, ENSEMBLE.
MIM HGNC e!Ensembl
614242 23520 ENSG00000165449
Protein
UniProt ID Q7RTY1
Protein name Monocarboxylate transporter 9 (MCT 9) (Solute carrier family 16 member 9)
Protein function Extracellular pH-and Na(+)-sensitive low-affinity creatine transporter (PubMed:31784090). Also functions as a pH-independent carnitine efflux transporter (PubMed:21886157).
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 13 423 Major Facilitator Superfamily Family
PF07690 MFS_1 305 501 Major Facilitator Superfamily Family
Sequence
Sequence length 509
Interactions View interactions
Associated diseases Disease information provided by ClinVar, GenCC, and GWAS databases.
Causal
Disease term Disease name dbSNP ID References
Kidney disease Chronic Kidney Diseases rs74315342, rs749740335, rs757649673, rs112417755, rs35138315 29545352
Unknown
Disease term Disease name Evidence References Source
Alopecia Areata Alopecia Areata GWAS
Gout Gout GWAS
Glioblastoma Glioblastoma CRISPR screening of E3 ubiquitin ligases reveals Ring Finger Protein 185 as a novel tumor suppressor in glioblastoma repressed by promoter hypermethylation and miR-587 GWAS, CBGDA
Associations from Text Mining
Disease Name Relationship Type References
Adenoma Associate 32566650
Colitis Ulcerative Associate 32566650
Colorectal Neoplasms Associate 32566650, 36854781
Gout Associate 23990105, 32090094
Iron Overload Associate 23990105
Juvenile gout Associate 23990105
Leiomyoma Associate 36948524
Neoplasms Associate 32566650, 36948524
Triple Negative Breast Neoplasms Associate 38171333