CTH wt Allele - CISMeF

Preferred Label : CTH wt Allele;

NCIt synonyms : Homoserine Dehydratase Gene; Cystathionase (Cystathionine Gamma-Lyase) Gene; CSE; Cystathionine Gamma-Lyase wt Allele; CGL; Homoserine Deaminase Gene;

NCIt definition : Human CTH wild-type allele is located in the vicinity of 1p31.1 and is approximately 29 kb in length. This allele, which encodes cystathionine gamma-lyase protein, plays a role in cleaving L,L-cystathionine into L-cysteine, ammonia and 2-oxobutanoate. Mutation of the gene is associated with cystathioninuria.;

NCI Metathesaurus CUI : CL1907110;

GenBank Accession Number : BC015807;

Details

Origin ID

C200289;

UMLS CUI

C5849064;

OMIM relation
- Cystathionine gamma-lyase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 1p31.3 [NCIt concept]
gene_is_element_in_pathway
- Cysteine and Methionine Metabolism Pathway [NCIt concept]
- Glycine, Serine and Threonine Metabolism Pathway [NCIt concept]
- Selenoamino Acid Metabolism Pathway [NCIt concept]
gene_plays_role_in_process
- Amino Acid Biosynthesis [NCIt concept]

Keyword's position in hierarchy(ies) :

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