======= CHDH ======= == Gene Information == * **Official Symbol**: CHDH * **Official Name**: choline dehydrogenase * **Aliases and Previous Symbols**: N/A * **Entrez ID**: [[https://www.ncbi.nlm.nih.gov/gene/?term=55349|55349]] * **UniProt**: [[https://www.uniprot.org/uniprot/Q8NE62|Q8NE62]] * **Interactions**: [[https://thebiogrid.org/search.php?search=CHDH&organism=9606|BioGRID]] * **PubMed articles**: [[https://www.ncbi.nlm.nih.gov/pubmed/?term=gene%20CHDH|Open PubMed]] * **OMIM**: N/A == Function Summary == * **Entrez Summary**: The protein encoded by this gene is a choline dehydrogenase that localizes to the mitochondrion. Variations in this gene can affect susceptibility to choline deficiency. A few transcript variants have been found for this gene, but the full-length nature of only one has been characterized to date. [provided by RefSeq, Dec 2010]. * **UniProt Summary**: N/A |GMC oxred N| |GMC oxred C| |choline dehydrogenase activity| |glycine betaine biosynthetic process| |glycine betaine biosynthetic process from choline| |glycine betaine metabolic process| |choline catabolic process| |amino-acid betaine biosynthetic process| |choline metabolic process| |amino-acid betaine metabolic process| |amine catabolic process| |cellular biogenic amine catabolic process| |neurotransmitter catabolic process| |cellular modified amino acid biosynthetic process| |cellular biogenic amine metabolic process| |cellular amine metabolic process| |flavin adenine dinucleotide binding| |amine metabolic process| |neurotransmitter metabolic process| |ammonium ion metabolic process| |cellular modified amino acid metabolic process| |regulation of neurotransmitter levels| |mitochondrial inner membrane| |oxidation-reduction process| |organonitrogen compound catabolic process| |organonitrogen compound biosynthetic process| |cellular nitrogen compound biosynthetic process| |organic substance catabolic process| |cellular catabolic process| \\ === CRISPR Data === ^Screen^Score^ |[[:results:exp106|UM131593 0.2μM R03 exp106]]|-2| ^Gene^Correlation^ |[[:human genes:p:prim1|PRIM1]]|0.409| 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**: 5194 * **Expression level (log2 read counts)**: 2.86 {{:chemogenomics:nalm6 dist.png?nolink |}}