======= SLC1A4 ======= == Gene Information == * **Official Symbol**: SLC1A4 * **Official Name**: solute carrier family 1 member 4 * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=6509|6509]] * **UniProt**: [[https://www.uniprot.org/uniprot/P43007|P43007]] * **Interactions**: [[https://thebiogrid.org/search.php?search=SLC1A4&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20SLC1A4|Open PubMed]] * **OMIM**: [[https://omim.org/entry/600229|Open OMIM]] == Function Summary == * **Entrez Summary**: The protein encoded by this gene is a sodium-dependent neutral amino acid transporter for alanine, serine, cysteine, and threonine. Defects in this gene have been associated with developmental delay, microcephaly, and intellectual disability. [provided by RefSeq, Jan 2017]. * **UniProt Summary**: Transporter for alanine, serine, cysteine, and threonine. Exhibits sodium dependence. {ECO:0000269|PubMed:26041762}. |SDF| |L-hydroxyproline transmembrane transporter activity| |threonine transport| |hydroxyproline transport| |L-threonine transmembrane transporter activity| |L-cystine transport| |L-cystine transmembrane transporter activity| |L-glutamine transmembrane transporter activity| |L-serine transport| |L-serine transmembrane transporter activity| |glutamine transport| |L-proline transmembrane transporter activity| |proline transmembrane transport| |L-alanine transmembrane transporter activity| |serine transport| |L-alanine transport| |sulfur amino acid transport| |proline transport| |alanine transport| |modified amino acid transport| |synaptic transmission, glutamatergic| |neutral amino acid transport| |amino acid transmembrane transporter activity| |symporter activity| |sulfur compound transport| |chloride channel activity| |L-amino acid transport| |amino acid transmembrane transport| |chloride transmembrane transport| |melanosome| |chloride transport| |inorganic anion transmembrane transport| |intermediate filament| |amino acid transport| |organic acid transmembrane transport| |carboxylic acid transmembrane transport| |microtubule organizing center| |inorganic anion transport| |anion transmembrane transport| |carboxylic acid transport| |organic acid transport| |cognition| |neuronal cell body| |anterograde trans-synaptic signaling| |dendrite| |chemical synaptic transmission| |trans-synaptic signaling| |organic anion transport| |synaptic signaling| |centrosome| |anion transport| |cation transmembrane transport| |cell surface| |inorganic ion transmembrane transport| |cation transport| |ion transmembrane transport| |cell-cell signaling| |transmembrane transport| |ion transport| |nervous system process| |integral component of plasma membrane| |nitrogen compound transport| |system process| |membrane| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp209|Deguelin 0.15μM R05 exp209]]|-1.71| |[[:results:exp485|GSK626616 14μM R08 exp485]]|1.73| |[[:results:exp351|Dexamethasone 0.006μM R07 exp351]]|1.77| |[[:results:exp231|Epothilone-B 0.0015μM R05 exp231]]|1.84| No correlation found to any other genes in chemogenomics. 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**: 12039 * **Expression level (log2 read counts)**: 6.18 {{:chemogenomics:nalm6 dist.png?nolink |}}