66 phenotypes from 4 alleles in 7 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Pgap1em1(IMPC)J/Pgap1em1(IMPC)J C57BL/6NJ-Pgap1em1(IMPC)J/Mmjax	preweaning lethality, complete penetrance	J:211773
Pgap1m1Nisw/Pgap1m1Nisw involves: 129S1/SvImJ * C57BL/6J	abnormal eye morphology	J:187360
	holoprosencephaly	J:187360
Pgap1m1Nisw/Pgap1m1Nisw involves: C57BL/6J	abnormal cranial cartilage morphology	J:187360
	abnormal cranium morphology	J:187360
	abnormal forebrain development	J:187360
	abnormal interparietal bone morphology	J:187360
	abnormal occipital bone morphology	J:187360
	absent basioccipital bone	J:187360
	decreased fetal size	J:187360
	forebrain hypoplasia	J:187360
	holoprosencephaly	J:101977, J:187360
Pgap1m1Nisw/Pgap1m1Nisw Tg(Hhex-EGFP)#Rbe/0 involves: C57BL/6 * C57BL/6J * CBA/J	abnormal anterior definitive endoderm morphology	J:187360
	abnormal anterior visceral endoderm cell migration	J:187360
	abnormal anterior visceral endoderm morphology	J:187360
	abnormal distal visceral endoderm morphology	J:187360
Pgap1oto/Pgap1+ involves: STOCK In(1)1Rk/J	abnormal sternum morphology	J:41878
	cervical vertebral transformation	J:41878
	lumbar vertebral transformation	J:41878
	vertebral transformation	J:41878
Pgap1oto/Pgap1oto B6.Cg-Pgap1oto	anophthalmia	J:151594
	decreased survivor rate	J:151594
	infertility	J:151594
	prenatal lethality, incomplete penetrance	J:151594
	small embryonic telencephalon	J:151594
Pgap1oto/Pgap1oto involves: STOCK In(1)1Rk/J	abnormal brain development	J:7938
	abnormal cranium morphology	J:7938
	abnormal diencephalon morphology	J:41878
	abnormal eye morphology	J:41878
	abnormal facial morphology	J:7938
	abnormal forebrain morphology	J:41878
	abnormal medial nasal prominence morphology	J:7938
	abnormal neural tube morphology	J:7938
	abnormal oropharynx morphology	J:41878
	abnormal outer ear morphology	J:41878
	abnormal sternum morphology	J:41878
	abnormal telencephalon development	J:7938
	abnormal telencephalon morphology	J:41878
	absent auditory tube	J:41878
	absent mandible	J:7938, J:41878
	absent Rathke's pouch	J:41878
	anophthalmia	J:41878
	cervical vertebral transformation	J:41878
	cyclopia	J:7938, J:41878
	fused first pharyngeal arch	J:41878
	increased rib number	J:41878
	lumbar vertebral transformation	J:41878
	microcephaly	J:41878
	micrognathia	J:41878
	microphthalmia	J:7938, J:41878
	narrow face	J:7938
	ocular hypotelorism	J:41878
	otocephaly	J:7938, J:41878
	proboscis	J:41878
	small embryonic telencephalon	J:41878
	small forehead	J:41878
	small mandible	J:41878
	thoracic vertebral transformation	J:41878
	truncated foregut	J:41878
	vertebral transformation	J:41878
Pgap1tm1Osb/Pgap1tm1Osb involves: 129S2/SvPas	abnormal brain morphology	J:126766
	abnormal cerebral cortex morphology	J:126766
	abnormal face shape	J:126766
	abnormal head development	J:126766
	abnormal telencephalon development	J:126766
	absent gastric milk in neonates	J:126766
	absent maxilla	J:126766
	absent nasal cavity	J:126766
	absent olfactory bulb	J:126766
	absent paranasal sinus	J:126766
	impaired binding of sperm to zona pellucida	J:126766
	impaired fertilization	J:126766
	impaired sperm migration in female genital tract	J:126766
	male infertility	J:126766
	otocephaly	J:126766
	perinatal lethality, incomplete penetrance	J:126766
	postnatal growth retardation	J:126766
	small mandible	J:126766