Gene Gene information from NCBI Gene database.
Entrez ID 151473
Gene name Solute carrier family 16 member 14
Gene symbol SLC16A14
Synonyms (NCBI Gene)
MCT14
Chromosome 2
Chromosome location 2q36.3
miRNA miRNA information provided by mirtarbase database.
389
miRTarBase ID miRNA Experiments Reference
MIRT019594 hsa-miR-340-5p Sequencing 20371350
MIRT024456 hsa-miR-215-5p Microarray 19074876
MIRT026583 hsa-miR-192-5p Microarray 19074876
MIRT546485 hsa-miR-6835-3p PAR-CLIP 20371350
MIRT546484 hsa-miR-548ad-3p PAR-CLIP 20371350
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
9
GO ID Ontology Definition Evidence Reference
GO:0005886 Component Plasma membrane IBA
GO:0005886 Component Plasma membrane IEA
GO:0008028 Function Monocarboxylic acid transmembrane transporter activity IBA
GO:0015293 Function Symporter activity IEA
GO:0015718 Process Monocarboxylic acid transport IEA
Other IDs Other IDs provides unique identifiers for this gene in OMIM, HGNC, and Ensembl databases.
MIM HGNC e!Ensembl
HGNC N/A HGNC
Protein Protein information from UniProt database.
UniProt ID Unique identifier for the protein in the UniProt database. Click to view detailed protein information.
Q7RTX9
Protein name Monocarboxylate transporter 14 (MCT 14) (Solute carrier family 16 member 14)
Protein function Proton-linked monocarboxylate transporter. May catalyze the transport of monocarboxylates across the plasma membrane.
Family and domains

Pfam

Accession ID Position in sequence Description Type
PF07690 MFS_1 40 428 Major Facilitator Superfamily Family
PF07690 MFS_1 417 504 Major Facilitator Superfamily Family
Sequence
Sequence length 510
Interactions View interactions
Associated diseases Disease associations from ClinVar (causal & non-causal) and other databases (OMIM, Orphanet, GWAS, etc.).
2
Evidence Score: ★☆☆☆☆  Gene-disease association found in Text Mining only ★★☆☆☆  Found in Text Mining and Unknown/Other Associations ★★★☆☆  Reported in Unknown/Other Associations across ≥2 Sources ★★★★☆  ClinVar: Pathogenic/Likely Pathogenic (<5 Variants) ★★★★★  ClinVar: Pathogenic/Likely Pathogenic (≥5 Variants)
Unknown / Other Associations ClinVar entries with uncertain/conflicting evidence, and associations from other databases (OMIM, Orphanet, GWAS, etc.) where the gene is not established as causal.
Phenotype Name Clinical Significance Source Evidence Score
ESOPHAGEAL SQUAMOUS CELL CARCINOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
OBSESSIVE-COMPULSIVE DISORDER GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text Mining Disease associations identified through text mining
Disease Name Disease (Merged) Source PMID Relationship Type Evidence Score
Mouth Neoplasms Mouth neoplasm Pubtator 27232157 Associate
★☆☆☆☆
Found in Text Mining only