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Protein Coding Gene : Relt RELT tumor necrosis factor receptor
Primary Identifier  MGI:2443373 Organism  mouse, laboratory
Chromosome  7 NCBI Gene Number  320100
Mgi Type  protein coding gene
description  FUNCTION: Automated description from the Alliance of Genome Resources (Release 7.1.0)

Involved in amelogenesis. Predicted to be located in nucleoplasm. Is expressed in female associated reproductive structure and urethra of female. Used to study amelogenesis imperfecta type 3C. Human ortholog(s) of this gene implicated in amelogenesis imperfecta type 3C. Orthologous to human RELT (RELT TNF receptor).
PHENOTYPE: Mice with a premature termination codon resulting in a null allele exhibit incisor and molar enamel malformations. Homozygous knockout affects T cell proliferation and reduces tumor growth. [provided by MGI curators]
  • synonyms:
  • E430021K24Rik,
  • tumor necrosis factor receptor superfamily, member 19-like,
  • Tnfrsf19l,
  • RIKEN cDNA E430021K24 gene,
  • Relt,
  • RELT tumor necrosis factor receptor
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0 Canonical

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2 Involved In Mutations

Trail: ProteinCodingGene

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