======= 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 |}}