Symbol
Name
ID
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Synonyms
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nmf231
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Genetic Map
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Alleles
and
phenotypes
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All alleles(3) :
Spontaneous(2)
Chemically induced(1)
| Mice homozygous for the variably penetrant curly-tail mutation (ct) may show symptoms of cranial or spinal neural tube defects such as curly tails and/or spina bifida; mice with these defects may survive beyond birth. Homozygotes with more severe phenotypes display exencephaly and die in utero. |
Phenotype Images (1)
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Gene Ontology
(GO)
classifications
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Other database
links
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References
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(Earliest)
J:264
Gruneberg H,
"Genetical studies on the skeleton of the mouse. VIII. Curly-tail"
J Genet 1954;52():52-67
(Latest)
J:129979
Gustavsson P et al.,
"Increased expression of Grainyhead-like-3 rescues spina bifida in a folate-resistant mouse model."
Hum Mol Genet 2007 Nov 1;16(21):2640-6
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All references(45)
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Other
accession IDs
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MGD-MRK-2211
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