help  | about  | cite  | software

Gene : CHDH Homo sapiens

Name  ? choline dehydrogenase Cytological Location  3p21.1
Brief Description  choline dehydrogenase
Description  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]
  • synonyms:
  • HGNC:24288,
  • OTTHUMG00000158281,
  • AJ272267,
  • NM_018397,
  • CHDH,
  • uc003dgz.4
  • identifiers:
  • 55349,
  • ENSG00000016391,
  • CHDH

Genome feature

Region: gene ? Length: 34130  
Location: 3:53812335-53846464 reverse strand Cyto location: 3p21.1

Uni Prot Comments Displayer

Protein Atlas Displayer

Gene Expression Atlas Tissues Displayer

Gene Expression Atlas Diseases Displayer

Publication Counts Displayer

Curated Proteins Displayer


Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


J Browse Displayer

Gene Structure Displayer

Overlapping Features Displayer

Mouse Alleles Displayer

Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.


Gene --> Proteins.


Gene Report --> GWAS hit


0 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]


Homologue Displayer


Cytoscape Network Displayer

Gene --> Physical and Genetic Interactions


Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.



3740 SN Ps

4 Cross References

16 Data Sets

19 Homologues

0 Located Features

97 Rna Seq Results