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Allele : Slc9a8<tm1d(KOMP)Wtsi> solute carrier family 9 (sodium/hydrogen exchanger), member 8; targeted mutation 1d, Wellcome Trust Sanger Institute

Primary Identifier  MGI:5925354 Allele Type  Targeted
Attribute String  Null/knockout Gene  Slc9a8
Transmission  Germline Strain of Origin  C57BL/6N
Is Recombinase  false Is Wild Type  false
Project Collection  KOMP-CSD
molecularNote  The L1L2_gt1 cassette was inserted at position 167282591 of Chromosome 2 upstream of the critical exon 4 (Build GRCm39). The cassette is composed of an FRT flanked lacZ/neomycin sequence followed by a loxP site. An additional loxP site is inserted downstream of exon 4 at position 167283331. Exon 4 is thus flanked by loxP sites. A null/knockout allele was created by flp and cre recombinase expression in mice carrying this allele to remove the lacZ sequence, neo selection cassette and the loxP-flanked exon 4. Western blot analysis confirmed the absence of protein expression in the male and female reproductive system and kidney of adult homozygous mutant mice.
  • mutations:
  • Intragenic deletion
  • synonyms:
  • Nhe8<->,
  • Nhe8<->
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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

5 Publication categories