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Allele : Trem2<em3Npa> triggering receptor expressed on myeloid cells 2; endonuclease-mediated mutation 3, Novartis Pharma AG

Primary Identifier  MGI:7509136 Allele Type  Endonuclease-mediated
Gene  Trem2 Strain of Origin  C57BL/6J
Is Recombinase  false Is Wild Type  false
molecularNote  CRISPR/Cas9 technology introduced a stop-codon (TGA) after the amino acid histidine 157 into the cleavage-site of TREM2. In addition, a restriction enzyme site Eco57I (CACTGAAGC) replaced the wild-type amino acids histidine, serine and threonine (HST; CACAGCACC). FACS confirmed absence of protein on the cell surface of bone marrow derived macrophages of homozygotes and soluble TREM2 levels are highly reduced. RNA levels are reduced in brain and may account for the reduced soluble protein levels.
  • mutations:
  • Nucleotide substitutions
  • synonyms:
  • TREM2-sol,
  • TREM2-sol
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1 Feature

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

0 Carried By

0 Driven By

2 Publication categories