======= SLC16A12 ======= == Gene Information == * **Official Symbol**: SLC16A12 * **Official Name**: solute carrier family 16 member 12 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=387700|387700]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q6ZSM3|Q6ZSM3]] * **Interactions**: [[https://thebiogrid.org/search.php?search=SLC16A12&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SLC16A12|Open PubMed]] * **OMIM**: [[https://omim.org/entry/611910|Open OMIM]] == Function Summary == * **Entrez 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]. * **UniProt Summary**: Proton-linked monocarboxylate transporter that mediates creatine transport across the plasma membrane. {ECO:0000269|PubMed:23578822}. |MFS 1| |creatine transmembrane transporter activity| |creatine transmembrane transport| |monocarboxylic acid transmembrane transporter activity| |modified amino acid transport| |symporter activity| |drug transmembrane transport| |organic acid transmembrane transport| |carboxylic acid transmembrane transport| |monocarboxylic acid transport| |drug transport| |anion transmembrane transport| |carboxylic acid transport| |organic acid transport| |organic anion transport| |anion transport| |ion transmembrane transport| |response to drug| |transmembrane transport| |ion transport| |integral component of plasma membrane| |nitrogen compound transport| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp438|NN-Diethyl-meta-toluamide 500μM R08 exp438]]|-2.03| |[[:results:exp78|Pterostilbene 16μM R02 exp78]]|-1.93| |[[:results:exp170|Metformin 100 to 150μM on day4 R04 exp170]]|-1.75| |[[:results:exp533|TNF-alpha 44ng/ml R08 exp533]]|1.88| |[[:results:exp285|GW501516 25μM R06 exp285]]|1.93| |[[:results:exp52|Ribavirin 10μM R01 exp52]]|2.01| ^Gene^Correlation^ |[[:human genes:r:rrm1|RRM1]]|0.512| Global Fraction of Cell Lines Where Essential: 0/739 ^Tissue^Fraction Of Cell Lines Where Essential^ |1290807.0|0/1| |909776.0|0/1| |bile duct|0/28| |blood|0/28| |bone|0/26| |breast|0/33| |central nervous system|0/56| |cervix|0/4| |colorectal|0/17| |esophagus|0/13| |fibroblast|0/1| |gastric|0/16| |kidney|0/21| |liver|0/20| |lung|0/75| |lymphocyte|0/16| |ovary|0/26| |pancreas|0/24| |peripheral nervous system|0/16| |plasma cell|0/15| |prostate|0/1| |skin|0/24| |soft tissue|0/9| |thyroid|0/2| |upper aerodigestive|0/22| |urinary tract|0/29| |uterus|0/5| == Essentiality in NALM6 == * **Essentiality Rank**: 15134 * **Expression level (log2 read counts)**: 1.28 {{:chemogenomics:nalm6 dist.png?nolink |}}