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Protein Coding Gene : Cth cystathionine gamma lyase

Primary Identifier  MGI:1339968 Organism  mouse, laboratory
Chromosome  3 NCBI Gene Number  107869
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Enables L-cystine L-cysteine-lyase (deaminating) and cystathionine gamma-lyase activity. Involved in negative regulation of apoptotic process and positive regulation of canonical NF-kappaB signal transduction. Acts upstream of or within cellular response to leukemia inhibitory factor and negative regulation of apoptotic signaling pathway. Predicted to be located in cytosol. Predicted to be active in cytoplasm. Is expressed in several structures, including alimentary system; central nervous system; cranium; ear; and genitourinary system. Used to study cystathioninuria. Human ortholog(s) of this gene implicated in amino acid metabolic disorder and cystathioninuria. Orthologous to human CTH (cystathionine gamma-lyase).
PHENOTYPE: Mice homozygous for a null allele exhibit hypertension associated with impaired endothelium-dependent vasorelaxation. Mice homozygous for another knock-out allele exhibit normal blood pressure but sensitivty to a low cysteine diet. [provided by MGI curators]
  • synonyms:
  • cDNA sequence BC019483,
  • MGI:2139663,
  • RIKEN cDNA 0610010I13 gene,
  • MGI:2384807,
  • MGC:28655,
  • Cth,
  • cystathionine gamma lyase,
  • AI314617,
  • CSE,
  • BC019483,
  • MGI:1917588,
  • expressed sequence AI314617,
  • 0610010I13Rik

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