Phenotypes associated with this allele

• Allele Symbol: Del(2Hoxd8,Hoxd9-Hoxd13)1Cx
• Allele Name: deletion, Chr 2, Gregory A Cox 1
• Allele ID: MGI:3574364
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Del(2Hoxd8,Hoxd9-Hoxd13)1Cx/Del(2Hoxd8,Hoxd9-Hoxd13)1Cx	involves: NZW/LacJ	MGI:3616443

Genotype
MGI:3616443

hm1

• Allelic Composition: Del(2Hoxd8,Hoxd9-Hoxd13)1Cx/Del(2Hoxd8,Hoxd9-Hoxd13)1Cx
• Genetic Background: involves: NZW/LacJ

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

behavior/neurological

hindlimb paralysis ( J:103924 )

• complete hindlimb paralysis

nervous system

abnormal ventral spinal root morphology ( J:103924 )

• reduced dorso-lumbar plexus

• absent peroneal branch from dorso-lumbar plexus

• no dorso-sacral plexus

• 24th and 25th spinal roots transformed to 24th and 25th

• only partial transformation of 23rd and 24th spinal roots to 22nd and 23rd

muscle

muscular atrophy ( J:103924 )

• severe atrophy of anterolateral leg compartment muscles