Gene Gene information from NCBI Gene database.
Entrez ID 201232
Gene name Solute carrier family 16 member 13
Gene symbol SLC16A13
Synonyms (NCBI Gene)
MCT13
Chromosome 17
Chromosome location 17p13.1
miRNA miRNA information provided by mirtarbase database.
169
miRTarBase ID miRNA Experiments Reference
MIRT036385 hsa-miR-1229-3p CLASH 23622248
MIRT670708 hsa-miR-383-3p HITS-CLIP 23824327
MIRT670707 hsa-miR-4493 HITS-CLIP 23824327
MIRT670706 hsa-miR-4533 HITS-CLIP 23824327
MIRT670705 hsa-miR-3202 HITS-CLIP 23824327
Gene ontology (GO) Gene Ontology (GO) annotations describing the biological processes, molecular functions, and cellular components associated with a gene.
13
GO ID Ontology Definition Evidence Reference
GO:0000139 Component Golgi membrane IEA
GO:0005515 Function Protein binding IPI 32296183
GO:0005794 Component Golgi apparatus IDA 24390345
GO:0005794 Component Golgi apparatus IEA
GO:0005829 Component Cytosol IDA
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.
Q7RTY0
Protein name Monocarboxylate transporter 13 (MCT 13) (Solute carrier family 16 member 13)
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 14 277 Major Facilitator Superfamily Family
PF07690 MFS_1 219 413 Major Facilitator Superfamily Family
Sequence
Sequence length 426
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
ASTROCYTOMA GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
TYPE 2 DIABETES MELLITUS GWAS catalog
★★☆☆☆
Found in Text Mining + Unknown/Other Associations
Associations from Text MiningDisease associations identified through Pubtator
Disease Name Relationship Type References Evidence Score
Carcinoma Non Small Cell Lung Associate 40022697
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Associate 34257700
★☆☆☆☆
Found in Text Mining only
Diabetes Mellitus Type 2 Associate 34257700, 37630718
★☆☆☆☆
Found in Text Mining only
Lung Neoplasms Associate 40022697
★☆☆☆☆
Found in Text Mining only
Neoplasms Associate 40022697
★☆☆☆☆
Found in Text Mining only
Pancreatic Neoplasms Associate 32355273
★☆☆☆☆
Found in Text Mining only