Ptchd1tm2.1Gfng
Targeted Allele Detail
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Symbol: |
Ptchd1tm2.1Gfng |
Name: |
patched domain containing 1; targeted mutation 2.1, Guoping Feng |
MGI ID: |
MGI:5792576 |
Synonyms: |
Ptchd1 fl |
Gene: |
Ptchd1 Location: ChrX:154356451-154406810 bp, - strand Genetic Position: ChrX, 72.38 cM
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Alliance: |
Ptchd1tm2.1Gfng page
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Allele Type: |
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Targeted (Conditional ready) |
Mutation: |
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Insertion
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Mutation details: A targeting vector containing a FRT-site flanked NEO selection cassette was used to insert loxP sites flanking exon 2. This selection cassette was inserted downstream of exon 2 of the targeted gene, and another loxP site was inserted upstream of exon 2. Flp-mediated recombination removed the selection cassette.
(J:232709)
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Key: |
hm |
homozygous |
ht |
heterozygous |
tg |
involves transgenes |
√ |
phenotype observed |
cn |
conditional genotype |
cx |
complex: > 1 genome feature |
ot |
other: hemizygous, indeterminate,... |
N |
normal phenotype |
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Genotype/ Background: |
| Allelic Composition | Genetic Background | Cell Line(s) |
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Loading... | | | involves: 129S1/Sv * 129S4/SvJae * 129X1/SvJ * C57BL/6J | |
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Phenotypes: |
Affected Systems |
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behavior/neurological
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behavior/neurological phenotype
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N
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abnormal cognition
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√
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hyperactivity
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√
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fragmentation of sleep/wake states
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√
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View phenotypes and curated references for all genotypes (concatenated display).
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Original: |
J:232709 Wells MF, et al., Thalamic reticular impairment underlies attention deficit in Ptchd1(Y/-) mice. Nature. 2016 Apr 7;532(7597):58-63 |
All: |
2 reference(s) |
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