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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Smo
smoothened, frizzled class receptor
MGI:108075
54 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Ankmy2tm1b(EUCOMM)Hmgu/Ankmy2tm1b(EUCOMM)Hmgu
Smotm1Amc/Smotm1Amc
involves: 129X1/SvJ * C57BL/6 * C57BL/6N
abnormal embryonic neuroepithelial layer differentiation J:297055
embryonic lethality between somite formation and embryo turning, complete penetrance J:297055
Atoh1tm3Hzo/Atoh1+
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1(Smo/EYFP)Amc
involves: 129 * 129S7/SvEvBrd * 129X1/SvJ
abnormal cerebellum external granule cell layer morphology J:155047
abnormal cerebellum morphology J:155047
abnormal neuronal precursor proliferation J:155047
irregular external granule cell layer thickness J:155047
Atoh1tm3Hzo/Atoh1tm1Hzo
Gt(ROSA)26Sortm1(cre/ERT)Nat/Gt(ROSA)26Sortm1(Smo/EYFP)Amc
involves: 129 * 129S7/SvEvBrd * 129X1/SvJ
abnormal neuronal precursor proliferation J:155047
cerebellum atrophy J:155047
thin external granule cell layer J:155047
Bmp4tm2Blh/Bmp4+
Smotm1Amc/Smotm1Amc
involves: 129S6/SvEvTac * 129X1/SvJ * C57BL/6
absent vitelline blood vessels J:128367
Cdcp1tm1.2Moas/Cdcp1tm1.2Moas
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sor+
Tg(KRT14-cre/ERT)20Efu/0
involves: 129X1/SvJ * C57BL/6 * CD-1 * FVB/N * SJL
abnormal skin condition J:194368
abnormal skin morphology J:194368
focal hair loss J:194368
hunched posture J:194368
increased tumor growth/size J:194368
increased tumor incidence J:194368
premature death J:194368
thick epidermis J:194368
thick skin J:194368
Cdk20tm1.1Jegg/Cdk20tm1.1Jegg
Smotm1Amc/Smotm1Amc
involves: 129S7/SvEvBrd * 129X1/SvJ * FVB/N
abnormal neuronal precursor cell number J:243907
En1tm2(cre)Wrst/?
Gli3tm1Alj/Gli3tm1Alj
Smotm2Amc/Smotm2Amc
involves: 129S1/Sv * 129S6/SvEvTac * 129X1/SvJ * C57BL/6
abnormal cerebellar foliation J:137136
abnormal cerebellum morphology J:137136
abnormal hindbrain morphology J:137136
abnormal rhombomere morphology J:137136
abnormal tectum morphology J:137136
enlarged cerebral aqueduct J:137136
enlarged tectum J:137136
normal nervous system phenotype J:137136
small cerebellum J:137136
thin external granule cell layer J:137136
Gli3tm1Alj/Gli3tm1Alj
Nkx3-2tm1(cre)Wez/Nkx3-2+
Smotm2Amc/Smotm2Amc
involves: 129S6/SvEvTac * 129S7/SvEvBrd * 129X1/SvJ
abnormal digestive system morphology J:199664
Gpr161tm1Lex/Gpr161tm1Lex
Smotm1Amc/Smotm1Amc
involves: 129S/SvEv * 129X1/SvJ * C57BL/6N
abnormal craniofacial morphology J:193395
abnormal neural tube morphology J:193395
normal growth/size/body region phenotype J:193395
Gt(ROSA)26Sortm1(Gli2)Jmao/Gt(ROSA)26Sor+
Smotm2Amc/Smotm2Amc
Nkx3-2tm1(cre)Wez/Nkx3-2+
involves: 129S1/Sv * 129S7/SvEvBrd * 129X1/SvJ
normal digestive/alimentary phenotype J:199664
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sor+
Hk2tm1.1Uku/Hk2+
Tg(GFAP-cre)25Mes/0
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N
increased medulloblastoma incidence J:210113
premature death J:210113
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sor+
Hk2tm1.1Uku/Hk2tm1.1Uku
Tg(GFAP-cre)25Mes/0
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * FVB/N
abnormal neuronal precursor proliferation J:210113
abnormal tumor vascularization J:210113
decreased tumor growth/size J:210113
increased medulloblastoma incidence J:210113
increased tumor latency J:210113
premature death J:210113
Gt(ROSA)26Sortm1(Smo/EYFP)Amc/Gt(ROSA)26Sortm2(EGFP/cre)Alj
Pgbd5tm1.1Aken/Pgbd5tm1.1Aken
involves: 129 * C57BL/6J * C57BL/6NTac * SW
increased medulloblastoma incidence J:346387
Gt(ROSA)26Sortm4(ACTB-tdTomato,-EGFP)Luo/?
Smotm2Amc/Smotm2Amc
Tg(Tagln-cre)1Jjl/0
involves: 129S1/Sv * 129X1/SvJ * FVB/N
normal cardiovascular system phenotype J:204743
Gt(ROSA)26Sortm6Dym/?
Smotm2Amc/Smotm2Amc
Sox9tm3(cre)Crm/Sox9+
involves: 129S7/SvEvBrd * 129X1/SvJ
abnormal temporomandibular joint morphology J:153743
small mandibular condyloid process J:153743
Ift122sopb/Ift122sopb
Smotm1Amc/Smotm1Amc
involves: 129X1/SvJ * C3Heb/FeJ * C57BL/6J
abnormal neural tube morphology J:168317
Ift172wim/Ift172wim
Smobnb/Smobnb
involves: C57BL/6J
abnormal direction of heart looping J:100466
decreased motor neuron number J:100466
embryonic lethality during organogenesis, complete penetrance J:100466
open neural tube J:100466
Kif7maki/Kif7maki
Smobnb/Smobnb
Tg(Hlxb9-GFP)1Tmj/?
involves: C57BL/6J * FVB/N
embryonic lethality during organogenesis, complete penetrance J:151965
normal nervous system phenotype J:151965
Kif7tm1.2Hui/Kif7tm1.2Hui
Smotm1Amc/Smotm1Amc
involves: 129S6/SvEvTac * 129X1/SvJ * CD-1
abnormal neural tube morphology J:152259
abnormal neuron differentiation J:152259
absent neuronal precursor cells J:152259
normal embryo phenotype J:152259
exencephaly J:152259
Mir34atm1.2Arte/Mir34a+
Tg(Neurod2-Smo*A1)199Jols/0
involves: C57BL/6 * C57BL/6N
increased medulloblastoma incidence J:221990
Mir34atm1.2Arte/Mir34atm1.2Arte
Tg(Neurod2-Smo*A1)199Jols/0
involves: C57BL/6 * C57BL/6N
increased medulloblastoma incidence J:221990
Smobnb/Smobnb
Tmem107schlei/Tmem107schlei
involves: C3HeB/FeJ * C57BL/6J
abnormal floor plate morphology J:186552
exencephaly J:186552
Smotm1Amc/Smotm1Amc
Tulp3hhkr/Tulp3hhkr
involves: 129X1/SvJ * C3H/HeH * C57BL/6
abnormal neural tube morphology J:147584
increased spinal cord size J:147584
pericardial edema J:147584
Smotm1Amc/Smotm1Amc
Wdpcpcys40/Wdpcpcys40
involves: 129X1/SvJ * C57BL/6J
abnormal embryo development J:205269
Smotm2Amc/Smotm2.1Amc
H2az2Tg(Wnt1-cre)11Rth/H2az2+
Gt(ROSA)26Sortm1Sor/Gt(ROSA)26Sor+
involves: 129S4/SvJaeSor * 129X1/SvJ * C57BL/6J * CBA/J
decreased cardiac neural crest cell number J:135134
impaired cardiac neural crest cell differentiation J:135134
Tctn1Gt(KST296)Byg/Tctn1Gt(KST296)Byg
Smotm1Amc/Smotm1Amc
involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6
increased forebrain size J:103820

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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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last database update
11/12/2024
MGI 6.24
The Jackson Laboratory