Del(13)36H
Radiation induced Allele Detail
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| Symbol: |
Del(13)36H |
| Name: |
deletion, Chr 13, Harwell 36 |
| MGI ID: |
MGI:3607783 |
| Synonyms: |
Del(13)Svea36H, Del36H |
| Gene: |
Del(13)36H Location: unknown Genetic Position: Chr13, cytoband A3.3-A5
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| Strain of Origin: |
(C3H/HeH x 101/H)F1
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| Allele Type: |
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Radiation induced |
| Mutation: |
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Intergenic deletion
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Del(13)36H involves 467 genes/genome features (n-TAagc7, n-TMcat2, A530084C06Rik ...)
View all
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Mutation details: This deletion, induced by X-irradiation of a (C3H/HeH x101/H)F1 female mouse, encompasses 12.66 Mb representing approximately 20% of mouse Chr 13 including bands A3.1 through A4. The deleted segment shares synteny with regions of human 6p25 and 6p22 associated with 6p deletion syndromes and 6p associated disorders.
(J:94183, J:101156)
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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 Del(13)36H Mutation: |
0 strains or lines available
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| Original: |
J:16316 Tease C, et al., Cytogenetic detection of four new, viable deletions in the progeny of X-irradiated females. Mouse Genome. 1993;91(4):855 |
| All: |
5 reference(s) |
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Analysis Tools
