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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		St14
suppression of tumorigenicity 14 (colon carcinoma)
MGI:1338881
23 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
F2rtm1Ajc/F2rtm1Ajc
St14tm1Bug/St14tm1Bug
involves: 129P2/OlaHsd * 129S4/SvJae 		normal embryo phenotype J:188121
normal mortality/aging J:188121
F2rl1tm1Cgh/F2rl1tm1Cgh
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
St14tm1Bug/St14+
involves: 129P2/OlaHsd * 129S4/SvJae 		exencephaly 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
Spint1tm1Bug/Spint1tm1Bug
St14Gt(XM184)Byg/St14Gt(XM184)Byg
involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss 		abnormal corneocyte morphology J:142708
abnormal epidermal layer morphology J:142708
abnormal epidermis stratum corneum morphology J:142708
absent gastric milk in neonates J:142708
absent vibrissae J:142708
dry skin J:142708
normal embryo phenotype J:142708
neonatal lethality, complete penetrance J:142708
reddish skin J:142708
thin epidermis J:142708
wrinkled skin J:142708
Spint1tm1Bug/Spint1tm1Bug
St14tm1Bug/St14+
involves: 129P2/OlaHsd * 129S6/SvEvTac 		absent placental labyrinth J:188121
embryonic lethality during organogenesis, complete penetrance J:188121
Spint1tm1Bug/Spint1tm1Bug
St14tm1Bug/St14tm1Bug
involves: 129P2/OlaHsd * 129S6/SvEvTac 		normal embryo phenotype J:188121
normal mortality/aging J:188121
Spint1tm1Bug/Spint1tm1Bug
St14tm1Bug/St14tm1Bug
involves: 129P2/OlaHsd * 129S6/SvEvTac * NIH Black Swiss 		abnormal corneocyte morphology J:142708
abnormal epidermal layer morphology J:142708
abnormal epidermis stratum corneum morphology J:142708
absent gastric milk in neonates J:142708
absent vibrissae J:142708
dry skin J:142708
normal embryo phenotype J:142708
neonatal lethality, complete penetrance J:142708
reddish skin J:142708
thin epidermis J:142708
wrinkled skin J:142708
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
St14tm1Bug/St14+
involves: 129P2/OlaHsd 		abnormal placenta labyrinth morphology J:188121
abnormal placenta morphology J:188121
curly tail J:188121
embryonic lethality between implantation and placentation, incomplete penetrance J:188121
embryonic lethality during organogenesis, incomplete penetrance J:188121
exencephaly J:188121
lethality throughout fetal growth and development, complete penetrance J:188121
spina bifida J:188121
Spint2Gt(KST272)Byg/Spint2Gt(KST272)Byg
St14tm1Bug/St14tm1Bug
involves: 129P2/OlaHsd 		abnormal neural tube morphology J:188121
curly tail J:188121
normal embryo phenotype J:188121
exencephaly J:188121
normal mortality/aging J:188121
spina bifida J:188121
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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
05/21/2024
MGI 6.23 		The Jackson Laboratory