CbllTg(Alb-KL)7-2Mhos
Transgenic Allele Detail
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Symbol: |
CbllTg(Alb-KL)7-2Mhos |
Name: |
cerebelless; transgene insertion 7-2, Mikio Hoshino |
MGI ID: |
MGI:3771564 |
Synonyms: |
cerebelless, Ptf1acbll |
Gene: |
Cbll Location: unknown Genetic Position: Chr2, Syntenic
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Alliance: |
CbllTg(Alb-KL)7-2Mhos page
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Strain of Origin: |
Not Specified
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Transgene Type: |
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Transgenic (Inserted expressed sequence, Null/knockout) |
Mutations: |
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Insertion, Intergenic deletion
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CbllTg(Alb-KL)7-2Mhos involves 2 genes/genome features (4921504E06Rik, Otud1)
View all
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Mutation details: A transgene insertion into chromosome 2 caused a nearby deletion event that disrupted the expression of several genes. A 313 kb deletion in chromosome 2 overlapped two genes, Otud1 and 4921522E24Rik, and disrupted the expression of a third upstream gene, Ptf1a. All three genes, which are normally expressed in the developing brain, had no expression in the cerebellum of E12.5 homozygotes. However, expression of Ptf1a in the pancreas was unaffected. The transgene that caused the deletion consisted of a mouse albumin enhancer and promoter fused to cDNA that encoded a secreted isoform of the human klotho gene. The transgene was expressed in the liver and the secreted protein was detectable in the serum of heterozygote mice. Mice homozygous for this transgene/deletion exhibit similar cerebellar defects as mice homozygous for a null allele of Ptf1a.
(J:100997)
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View phenotypes and curated references for all genotypes (concatenated display).
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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
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Carrying any Cbll Mutation: |
0 strains or lines available
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Original: |
J:100997 Hoshino M, et al., Ptf1a, a bHLH transcriptional gene, defines GABAergic neuronal fates in cerebellum. Neuron. 2005 Jul 21;47(2):201-13 |
All: |
4 reference(s) |
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