Homo sapiens Gene: SLC16A12
Summary
InnateDB Gene IDBG-81998.6
Last Modified 2014-10-13 [Report errors or provide feedback]
Gene Symbol SLC16A12
Gene Name solute carrier family 16, member 12 (monocarboxylic acid transporter 12)
Synonyms
Species Homo sapiens
Ensembl Gene ENSG00000152779
Encoded Proteins
solute carrier family 16, member 12 (monocarboxylic acid transporter 12)
solute carrier family 16, member 12 (monocarboxylic acid transporter 12)
Protein Structure
Useful resources Stemformatics EHFPI ImmGen
Entrez Gene
Summary This gene encodes a transmembrane transporter that likely plays a role in monocarboxylic acid transport. A mutation in this gene has been associated with juvenile cataracts with microcornea and renal glucosuria. [provided by RefSeq, Mar 2010]
Gene Information
Type Protein coding
Genomic Location Chromosome 10:89430299-89556641
Strand Reverse strand
Band q23.31
Transcripts
ENST00000371790 ENSP00000360855
ENST00000475682 ENSP00000436965
Interactions
Number of Interactions This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
Gene Ontology

Molecular Function
Accession GO Term
GO:0015293 symporter activity
Biological Process
GO:0055085 transmembrane transport
Cellular Component
GO:0005886 plasma membrane
GO:0016021 integral component of membrane
Orthologs
Species
Mus musculus
Bos taurus
Gene ID
Gene Order
Not yet available
Cross-References
SwissProt Q6ZSM3
TrEMBL E9PPP4 E9PSF9
UniProt Splice Variant
Entrez Gene 387700
UniGene Hs.530338
RefSeq NM_213606
HUGO HGNC:23094
OMIM 611910
CCDS CCDS7404
HPRD 17365
IMGT
EMBL AK124901 AK127303 AL353146 AL355342 BC086873
GenPept AAH86873 BAC85987 BAC86925 CAI12383
RNA Seq Atlas 387700