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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Del(2Hoxd10-Hoxd13)7Ddu
deletion, Chr 2, Denis Duboule 7
MGI:3616161
Summary 2 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Del(2Hoxd10-Hoxd13)7Ddu/Del(2Hoxd10-Hoxd13)7Ddu involves: 129S2/SvPas MGI:3616438
cn2
Del(2Hoxd10-Hoxd13)7Ddu/Del(2Hoxd10-Hoxd13)7Ddu
Hoxatm1Ddu/Del(6Hoxa)1Ddu
Tg(Prrx1-cre)1Cjt/0
involves: 129S2/SvPas * C57BL/6 * SJL MGI:3715858


Genotype
MGI:3616438
hm1
Allelic
Composition
Del(2Hoxd10-Hoxd13)7Ddu/Del(2Hoxd10-Hoxd13)7Ddu
Genetic
Background
involves: 129S2/SvPas
Find Mice Using the International Mouse Strain Resource (IMSR)
No mouse lines available in IMSR.
See publication links below for author information.
phenotype observed in females
phenotype observed in males
N normal phenotype
behavior/neurological
• complete hindlimb paralysis

nervous system
• reduced dorso-lumbar plexus
• absent peroneal branch from dorso-lumbar plexus
• no dorso-sacral plexus

muscle
• severe atrophy of anterolateral leg compartment muscles




Genotype
MGI:3715858
cn2
Allelic
Composition
Del(2Hoxd10-Hoxd13)7Ddu/Del(2Hoxd10-Hoxd13)7Ddu
Hoxatm1Ddu/Del(6Hoxa)1Ddu
Tg(Prrx1-cre)1Cjt/0
Genetic
Background
involves: 129S2/SvPas * C57BL/6 * SJL
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Del(2Hoxd10-Hoxd13)7Ddu mutation (0 available); any Del(2Hoxd10-Hoxd13)7Ddu mutation (0 available)
Del(6Hoxa)1Ddu mutation (0 available); any Del(6Hoxa)1Ddu mutation (0 available)
Hoxatm1Ddu mutation (0 available); any Hoxa mutation (0 available)
Tg(Prrx1-cre)1Cjt mutation (2 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
limbs/digits/tail
• no genuine forearm in newborn mice
• abnormal segmented cartilaginous condensation is present, instead of digits, radii, or ulnae
• no genuine digits form on forelimb in newborn mice

skeleton





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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory