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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Psip1
PC4 and SFRS1 interacting protein 1
MGI:2142116
54 phenotypes from 3 alleles in 5 genetic backgrounds
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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
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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
12/17/2024
MGI 6.24 		The Jackson Laboratory