29 phenotypes from 2 alleles in 2 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Kat6bGt(pKC199)1Pgr/Kat6b+ involves: 129S2/SvPas	decreased body weight	J:178264
Kat6bGt(pKC199)1Pgr/Kat6bGt(pKC199)1Pgr involves: 129S2/SvPas	abnormal cerebral cortex morphology	J:62161
	abnormal coronal suture morphology	J:62161
	abnormal cortical plate morphology	J:178264
	abnormal cranium morphology	J:62161
	abnormal ear position	J:62161, J:178264
	abnormal epiphyseal plate morphology	J:178264
	abnormal limb long bone morphology	J:178264
	abnormal long bone hypertrophic chondrocyte zone	J:178264
	abnormal muscle morphology	J:178264
	abnormal nasolacrimal duct morphology	J:62161, J:178264
	abnormal neuronal migration	J:178264
	abnormal occipital bone morphology	J:62161
	abnormal parietal bone morphology	J:62161
	abnormal telencephalon development	J:62161
	decreased body size	J:62161
	decreased body weight	J:62161
	decreased brain size	J:62161, J:178264
	decreased cerebral cortex pyramidal cell number	J:178264
	decreased inferior colliculus size	J:62161
	decreased percent body fat/body weight	J:178264
	delayed cranial suture closure	J:62161, J:178264
	microphthalmia	J:62161, J:178264
	postnatal growth retardation	J:62161, J:178264
	postnatal lethality, incomplete penetrance	J:62161
	short mandible	J:178264
	shortened head	J:62161
	small olfactory bulb	J:62161, J:178264
Kat6bm1Mhda/Kat6b+ C3HeB/FeJ-Kat6bm1Mhda	no abnormal phenotype detected	J:82809
Kat6bm1Mhda/Kat6bm1Mhda C3HeB/FeJ-Kat6bm1Mhda	prenatal lethality, complete penetrance	J:82809