======= MAP1LC3A ======= == Gene Information == * **Official Symbol**: MAP1LC3A * **Official Name**: microtubule associated protein 1 light chain 3 alpha * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=84557|84557]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q9H492|Q9H492]] * **Interactions**: [[https://thebiogrid.org/search.php?search=MAP1LC3A&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20MAP1LC3A|Open PubMed]] * **OMIM**: [[https://omim.org/entry/601242|Open OMIM]] == Function Summary == * **Entrez Summary**: N/A * **UniProt Summary**: Ubiquitin-like modifier involved in formation of autophagosomal vacuoles (autophagosomes) (PubMed:20713600, PubMed:24290141). Whereas LC3s are involved in elongation of the phagophore membrane, the GABARAP/GATE-16 subfamily is essential for a later stage in autophagosome maturation (PubMed:20713600). {ECO:0000269|PubMed:20713600, ECO:0000269|PubMed:24290141}. |Atg8| |APG12| |response to iron(II) ion| |autolysosome| |organelle membrane| |phosphatidylethanolamine binding| |cellular response to nitrogen starvation| |cellular response to nitrogen levels| |response to lead ion| |cellular response to copper ion| |response to isoquinoline alkaloid| |response to morphine| |response to iron ion| |autophagosome maturation| |autophagosome membrane| |autophagy of mitochondrion| |mitochondrion disassembly| |cellular response to amino acid starvation| |response to copper ion| |response to amino acid starvation| |autophagosome assembly| |organelle disassembly| |autophagosome organization| |autophagosome| |cellular response to hydrogen peroxide| |response to anesthetic| |phospholipid binding| |response to alkaloid| |cellular response to antibiotic| |response to hydrogen peroxide| |late endosome| |vacuole organization| |cellular response to reactive oxygen species| |cellular response to starvation| |macroautophagy| |response to ammonium ion| |cellular response to metal ion| |response to starvation| |response to reactive oxygen species| |cellular response to toxic substance| |cellular response to inorganic substance| |cellular response to nutrient levels| |microtubule binding| |protein-containing complex disassembly| |cellular response to oxidative stress| |autophagy| |process utilizing autophagic mechanism| |cellular response to extracellular stimulus| |synapse| |ubiquitin protein ligase binding| |response to xenobiotic stimulus| |response to antibiotic| |microtubule| |cellular response to external stimulus| |response to metal ion| |response to oxidative stress| |cellular component disassembly| |cellular response to drug| |mitochondrion organization| |response to nutrient levels| |response to toxic substance| |response to extracellular stimulus| |response to inorganic substance| |organelle assembly| |response to organic cyclic compound| |response to organonitrogen compound| |response to drug| |cellular response to oxygen-containing compound| |response to nitrogen compound| |response to oxygen-containing compound| |cellular response to stress| |cellular catabolic process| |protein-containing complex subunit organization| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp40|2-Methoxyestradiol 0.2μM R01 exp40]]|-1.94| 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**: 7935 * **Expression level (log2 read counts)**: -3.13 {{:chemogenomics:nalm6 dist.png?nolink |}}