Phenotypes Associated with This Genotype

Genotype
MGI:2451170

• Allelic Composition: Sox9^tm2Crm/Sox9^tm2Crm; Tg(Col2a1-cre)1Bhr/0
• Genetic Background: involves: 129S7/SvEvBrd * C57BL/6 * SJL

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

mortality/aging

lethality throughout fetal growth and development, incomplete penetrance ( J:79879 )

• embryos die around day E16.5; only a few are recovered after birth

craniofacial

short snout ( J:79879 )

growth/size/body

short snout ( J:79879 )

decreased body length ( J:79879 )

distended abdomen ( J:79879 )

limbs/digits/tail

short limbs ( J:79879 )

short tail ( J:79879 )

skeleton

chondrodystrophy ( J:79879 )

• severe

Mouse Models of Human Disease		DO ID	OMIM ID(s)	Ref(s)
campomelic dysplasia		DOID:0050463	OMIM:114290	J:79879