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| Nomenclature |
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Symbol:
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Arxtm1Kki
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Name:
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aristaless related homeobox;
targeted mutation 1, Kunio Kitamura
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MGI ID: |
MGI:2429693 |
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Synonyms: |
ArxX* |
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Gene:
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Arx
Location:
ChrX:93286507-93298357 bp, + strand
Genetic Position: ChrX,
41.05 cM
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Mutation
origin |
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Germline Transmission:
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Earliest citation of germline transmission:
J:79871
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Parent Cell Line:
| E14TG2a (ES Cell) |
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Strain of Origin:
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129P2/OlaHsd
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Mutation
description |
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Allele
Type: | |
Targeted (Reporter) |
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Mutation: | |
Insertion |
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Mutation details: The gene was disrupted by insertion of a STOP-IRES-lacZ-neo cassette into exon 2, which encodes a homeobox domain. (J:79871)
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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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| References |
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Original: |
J:79871
Kitamura K et al.,
"Mutation of ARX causes abnormal development of forebrain and testes in mice and X-linked lissencephaly with abnormal genitalia in humans."
Nat Genet 2002 Nov;32(3):359-69
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All: |
3 reference(s)
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Analysis Tools
