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Allele : Slc18a2<tm1Kmo> solute carrier family 18 (vesicular monoamine), member 2; targeted mutation 1, Katrin A Mooslehner

Primary Identifier  MGI:2182931 Allele Type  Targeted
Attribute String  Null/knockout Gene  Slc18a2
Transmission  Germline Strain of Origin  129P2/OlaHsd
Is Recombinase  false Is Wild Type  false
description  ES cell line = CGR8.8 (subline of CGR8)

molecularNote  Exons 1 and 2 and flanking intronic sequences were replaced with a neomycin resistance cassette via homologous recombination. Absence of gene expression in homozygous mutant neonates was demonstrated by RT-PCR analysis of total midbrain RNA using primers to exons 2 and 12.
  • mutations:
  • Insertion,
  • Intragenic deletion
  • synonyms:
  • GB1/1,
  • GB1/1
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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