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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Pgap1
post-GPI attachment to proteins 1
MGI:2443342
66 phenotypes from 4 alleles in 7 genetic backgrounds
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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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/19/2024
MGI 6.24 		The Jackson Laboratory