54 phenotypes from 3 alleles in 5 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Psip1em1(IMPC)J/Psip1+ C57BL/6NJ-Psip1em1(IMPC)J/Mmjax	decreased circulating creatinine level	J:211773
Psip1em1(IMPC)J/Psip1em1(IMPC)J C57BL/6NJ-Psip1em1(IMPC)J/Mmjax	embryonic growth retardation	J:211773
	preweaning lethality, complete penetrance	J:211773
Psip1Gt(betageo)1Hgs/Psip1+ B6.129P2-Psip1Gt(betageo)1Hgs	postnatal lethality, incomplete penetrance	J:112975
Psip1Gt(betageo)1Hgs/Psip1+ either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * MF1)	normal mortality/aging	J:112975
Psip1Gt(betageo)1Hgs/Psip1Gt(betageo)1Hgs B6.129P2-Psip1Gt(betageo)1Hgs	abnormal abdominal fat pad morphology	J:112975
	abnormal axial skeleton morphology	J:112975
	abnormal cervical atlas morphology	J:112975
	abnormal cervical axis morphology	J:112975
	abnormal cervical vertebrae morphology	J:112975
	abnormal cranium morphology	J:112975
	abnormal jaw morphology	J:112975
	abnormal neurocranium morphology	J:112975
	abnormal rib development	J:112975
	abnormal rib morphology	J:112975
	abnormal spine curvature	J:112975
	abnormal vertebrae morphology	J:112975
	absent epididymal fat pad	J:112975
	absent gastric milk in neonates	J:112975
	asymmetric rib joints	J:112975
	blepharitis	J:112975
	broad face	J:112975
	broad head	J:112975
	broad nasal bone	J:112975
	broad occipital bone	J:112975
	cervical vertebral transformation	J:112975
	decreased grip strength	J:112975
	decreased locomotor activity	J:112975
	decreased lumbar vertebrae number	J:112975
	decreased rib number	J:112975
	decreased total body fat amount	J:112975
	decreased vertical activity	J:112975
	domed cranium	J:112975
	flat occipital bone	J:112975
	hunched posture	J:112975
	limb grasping	J:112975
	lumbar vertebral transformation	J:112975
	perinatal lethality, incomplete penetrance	J:112975
	reduced male fertility	J:112975
	short face	J:112975
	short nasal bone	J:112975
	short sternum	J:112975
	shortened head	J:112975
	small exoccipital bone	J:112975
	small interparietal bone	J:112975
	small supraoccipital bone	J:112975
	small testis	J:112975
	spleen atrophy	J:112975
	thoracic vertebral transformation	J:112975
	vertebral transformation	J:112975
	normal vision/eye phenotype	J:112975
Psip1Gt(betageo)1Hgs/Psip1Gt(betageo)1Hgs either: (involves: 129P2/OlaHsd * C57BL/6) or (involves: 129P2/OlaHsd * MF1)	abnormal abdominal fat pad morphology	J:112975
	abnormal axial skeleton morphology	J:112975
	abnormal cervical atlas morphology	J:112975
	abnormal cervical axis morphology	J:112975
	abnormal cervical vertebrae morphology	J:112975
	abnormal cranium morphology	J:112975
	abnormal nasal bone morphology	J:112975
	abnormal neurocranium morphology	J:112975
	abnormal rib development	J:112975
	abnormal rib morphology	J:112975
	abnormal spine curvature	J:112975
	abnormal vertebrae morphology	J:112975
	absent epididymal fat pad	J:112975
	absent gastric milk in neonates	J:112975
	asymmetric rib joints	J:112975
	blepharitis	J:112975
	broad head	J:112975
	broad nasal bone	J:112975
	broad occipital bone	J:112975
	cervical vertebral transformation	J:112975
	decreased grip strength	J:112975
	decreased locomotor activity	J:112975
	decreased lumbar vertebrae number	J:112975
	decreased rib number	J:112975
	decreased total body fat amount	J:112975
	decreased vertical activity	J:112975
	domed cranium	J:112975
	flat occipital bone	J:112975
	hunched posture	J:112975
	limb grasping	J:112975
	lumbar vertebral transformation	J:112975
	perinatal lethality, incomplete penetrance	J:112975
	reduced male fertility	J:112975
	short face	J:112975
	short nasal bone	J:112975
	short sternum	J:112975
	shortened head	J:112975
	small exoccipital bone	J:112975
	small interparietal bone	J:112975
	small supraoccipital bone	J:112975
	small testis	J:112975
	spleen atrophy	J:112975
	thoracic vertebral transformation	J:112975
	vertebral transformation	J:112975
	normal vision/eye phenotype	J:112975
Psip1tm1Eng/Psip1tm1Eng involves: 129S6/SvEvTac * C57BL/6	no abnormal phenotype detected	J:177408
Psip1tm1Eng/Psip1tm1Eng Edil3Tg(Sox2-cre)1Amc/Edil3+ involves: 129S6/SvEvTac * C57BL/6 * CBA	abnormal cell physiology	J:177408