======= 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 |}}