======= 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 |}}