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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Prss8
serine protease 8 (prostasin)
MGI:1923810
27 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
F2rl1tm1Cgh/F2rl1tm1Cgh
Tg(KRT14-Prss8)2Hum/?
involves: 129S4/SvJae * C57BL/6 * DBA/2
normal integument phenotype J:189278
Oatrhg/Prss8fr
involves: AKR/J * C57BL/6JEi * FS/EiJ
no abnormal phenotype detected J:213842
Prss8em1Bug/Prss8em1Bug
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
involves: 129P2/OlaHsd * 129S6/SvEvTac * C57BL/6J * FVB/NJ * NIH Black Swiss
abnormal digestive system morphology J:261068
abnormal enterocyte proliferation J:261068
abnormal intestinal epithelium morphology J:261068
abnormal intestinal goblet cell morphology J:261068
abnormal intestine morphology J:261068
abnormal large intestine crypts of Lieberkuhn morphology J:261068
abnormal large intestine morphology J:261068
abnormal small intestine morphology J:261068
decreased birth weight J:261068
decreased colon goblet cell number J:261068
decreased intestine length J:261068
intestinal hemorrhage J:261068
postnatal growth retardation J:261068
postnatal lethality, complete penetrance J:261068
small intestinal villus atrophy J:261068
Prss8fr/Prss8+
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
involves: 129P2/OlaHsd * DBA
embryonic lethality, complete penetrance J:188121
Prss8fr/Prss8+
Spint1tm1Bug/Spint1tm1Bug
involves: 129S6/SvEvTac * DBA
abnormal placenta morphology J:188121
curly tail J:188121
embryonic lethality during organogenesis, complete penetrance J:188121
exencephaly J:188121
spina bifida J:188121
Prss8fr/Prss8fr
Spint1tm1Bug/Spint1tm1Bug
involves: 129S6/SvEvTac * DBA
abnormal coat appearance J:188121
normal embryo phenotype J:188121
prenatal lethality, incomplete penetrance J:188121
Prss8fr/Prss8fr
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
involves: 129P2/OlaHsd * DBA
normal embryo phenotype J:188121
exencephaly J:188121
prenatal lethality, incomplete penetrance J:188121
Prss8fr/Prss8fr
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
St14tm1Bug/St14+
involves: 129P2/OlaHsd * DBA
normal embryo phenotype J:188121
normal mortality/aging J:188121

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory