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Allele : Fgf14<tm1Dor> fibroblast growth factor 14; targeted mutation 1, David M Ornitz

Primary Identifier  MGI:2183403 Allele Type  Targeted
Attribute String  Null/knockout, Reporter Gene  Fgf14
Transmission  Germline Strain of Origin  129S6/SvEvTac
Is Recombinase  false Is Wild Type  false
description  Phenotypic Similarity to Human Syndrome: Paroxysmal dyskinesia (J:77806)
molecularNote  A cassette containing lacZ and neo genes was inserted into exon 2. The construct was designed such that a fusion protein, containing the alternatively spliced exon 1 and lacZ product, would be produced. The insertion deleted the majority of exon 2 and all of exon 3, which encode residues conserved in the FGF family. Transcript was undetected via Northern blot analysis of total cerebellar RNA obtained from homozygous mutant mice. While in situ hybridization and RNA blot analysis showed similar mRNA expression patterns between the mutant and endogenous alleles, protein expression patterns were shown to vary via X-gal staining.
  • mutations:
  • Intragenic deletion,
  • Insertion
  • synonyms:
  • Fgf14<N-Beta-Gal>,
  • Fgf14<N-Beta-Gal>
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1 Feature

Trail: Allele

Genome

0 Expresses

0 Mutation Involves

Phenotype

Mouse alleles --> Mammalian phenotypes (MP terms)

 

Other

2 Carried By

Trail: Allele

0 Driven By

15 Publication categories

Trail: Allele