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Slc18a2tm1Kmo
Targeted Allele Detail
Summary
Symbol: Slc18a2tm1Kmo
Name: solute carrier family 18 (vesicular monoamine), member 2; targeted mutation 1, Katrin A Mooslehner
MGI ID: MGI:2182931
Synonyms: GB1/1
Gene: Slc18a2  Location: Chr19:59249328-59284444 bp, + strand  Genetic Position: Chr19, 54.64 cM
Alliance: Slc18a2tm1Kmo page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:70606
Parent Cell Line:  CGR8 (ES Cell)
Strain of Origin:  129P2/OlaHsd
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutations:    Insertion, Intragenic deletion
 
Mutation detailsExons 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. (J:70606)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Slc18a2 Mutation:  29 strains or lines available
Notes
ES cell line = CGR8.8 (subline of CGR8)

References
Original:  J:70606 Mooslehner KA, et al., Mice with very low expression of the vesicular monoamine transporter 2 gene survive into adulthood: potential mouse model for parkinsonism. Mol Cell Biol. 2001 Aug;21(16):5321-31
All:  2 reference(s)

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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last database update
04/30/2024
MGI 6.23
The Jackson Laboratory