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| Nomenclature |
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Symbol:
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Tlx3tm1Sjk
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Name:
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T cell leukemia, homeobox 3;
targeted mutation 1, Stanley J Korsmeyer
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MGI ID: |
MGI:2180105 |
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Synonyms: |
Rnx-, Tlx3- |
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Gene:
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Tlx3
Location:
Chr11:33200752-33203588 bp, - strand
Genetic Position: Chr11,
19.21 cM, cytoband A5
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Mutation origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:60751
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Parent Cell Line:
| RW-4 (ES Cell) |
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Strain of Origin:
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129X1/SvJ
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Mutation description |
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Allele
Type: | |
Targeted (knock-out) |
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Mutations: | |
Insertion, Intragenic deletion |
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Mutation details: A PGK-neo cassette was inserted into exon 1. RNA in situ analysis confirmed the lack of gene expression in homozygous mice. (J:60751)
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Phenotypes
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View phenotypes for all genotypes (concatenated display).
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Disease models
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| Find Mice (IMSR) |
Mouse strains and cell lines available from the
International Mouse Strain Resource
(IMSR)
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Carrying this Mutation: |
Mouse Strains: 0 strains available
Cell Lines: 0 lines available |
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Carrying any Tlx3 Mutation:
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4 strains or lines available |
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| References |
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Original: |
J:60751
Shirasawa S et al.,
"Rnx deficiency results in congenital central hypoventilation."
Nat Genet 2000 Mar;24(3):287-90
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All: |
11 reference(s)
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