TAT wt Allele - CISMeF

Preferred Label : TAT wt Allele;

NCIt synonyms : Tyrosine Aminotransferase, Cytosolic Gene; Tyrosine Aminotransferase wt Allele;

NCIt definition : Human TAT wild-type allele is located in the vicinity of 16q22.2 and is approximately 11 kb in length. This allele, which encodes tyrosine aminotransferase protein, is involved in the catabolism of tyrosine. Mutation in the gene is associated with tyrosinemia type 2 (Richner-Hanhart syndrome).;

NCI Metathesaurus CUI : CL1642996;

GenBank Accession Number : NM_000353;

Détails

Origin ID

C177225;

UMLS CUI

C5443962;

OMIM relation
- Tyrosine aminotransferase [OMIM gene]
Semantic type(s)
- Gene or Genome [UMLS semantic type]
gene_found_in_organism
- Human [NCIt concept]
gene_in_chromosomal_location
- 16q22.2 [NCIt concept]
gene_is_element_in_pathway
- Cysteine and Methionine Metabolism Pathway [NCIt concept]
- FOXA2 and FOXA3 Transcription Factor Signaling Pathway [NCIt concept]
- Glucocorticoid Receptor Regulatory Network [NCIt concept]
- HDAC Class III Signaling Pathway [NCIt concept]
- Phenylalanine Metabolism Pathway [NCIt concept]
- Phenylalanine, Tyrosine and Tryptophan Biosynthesis Pathway [NCIt concept]
- Tyrosine Metabolism Pathway [NCIt concept]
- Ubiquinone Biosynthesis Pathway [NCIt concept]
gene_plays_role_in_process
- Catabolic Process [NCIt concept]

Position du mot-clé dans l'(les) arborescence(s) :

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