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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Smarcb1
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1
MGI:1328366
33 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ccnd1tm1Wbg/Ccnd1tm1Wbg
Smarcb1tm1Gvk/Smarcb1+
involves: 129/Sv * 129S2/SvPas * C57BL/6J * SJL/J 		abnormal eye development J:101185
abnormal nervous system development J:101185
decreased body size J:101185
decreased tumor incidence J:101185
Smarcb1tm1Sho/Smarcb1+
Tg(LPV-TAg121)2Tvd/0
involves: 129S6/SvEvTac * C57BL/6J * DBA/2J 		increased carcinoma incidence J:120820
increased malignant tumor incidence J:120820
Smarcb1tm2Sho/Smarcb1+
Trp53tm1Brn/Trp53+
Tg(GFAP-cre)#Gtm/0
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA 		excessive scratching J:226786
Smarcb1tm2Sho/Smarcb1+
Trp53tm1Brn/Trp53tm1Brn
Tg(GFAP-cre)#Gtm/0
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA 		excessive scratching J:226786
Smarcb1tm2Sho/Smarcb1tm2Sho
Trp53tm1Brn/Trp53+
Tg(GFAP-cre)#Gtm/0
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA 		abnormal brain white matter morphology J:226786
normal neoplasm J:226786
Smarcb1tm2Sho/Smarcb1tm2Sho
Trp53tm1Brn/Trp53tm1Brn
Tg(GFAP-cre)#Gtm/0
involves: 129P2/OlaHsd * 129S1/Sv * C57BL/6 * CBA 		abnormal brain white matter morphology J:226786
abnormal cerebellar granule cell migration J:226786
abnormal cerebellar layer morphology J:226786
abnormal cerebellum external granule cell layer morphology J:226786
abnormal cerebellum morphology J:226786
abnormal cerebral cortex morphology J:226786
abnormal corpus callosum morphology J:226786
abnormal gait J:226786
abnormal hippocampus morphology J:226786
abnormal limb posture J:226786
abnormal locomotor behavior J:226786
abnormal stride length J:226786
ataxia J:226786
circling J:226786
decreased body size J:226786
decreased body weight J:226786
decreased oligodendrocyte number J:226786
decreased survivor rate J:226786
dystonia J:226786
excessive scratching J:226786
gliosis J:226786
hindlimb paralysis J:226786
impaired coordination J:226786
increased brain tumor incidence J:226786
lethargy J:226786
seizures J:226786
tremors J:226786
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
04/16/2024
MGI 6.23 		The Jackson Laboratory