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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Pds5b
PDS5 cohesin associated factor B
MGI:2140945
21 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Pds5aGt(RRM243)Byg/Pds5a+
Pds5btm1Jmi/Pds5btm1Jmi
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal enteric nervous system morphology J:148890
abnormal heart morphology J:148890
abnormal interventricular septum morphology J:148890
abnormal nervous system morphology J:148890
absent aorticopulmonary septum J:148890
absent atrioventricular cushions J:148890
aphakia J:148890
common atrioventricular valve J:148890
common truncal valve J:148890
complete atrioventricular septal defect J:148890
conotruncal ridge hypoplasia J:148890
dilated heart atrium J:148890
embryonic growth retardation J:148890
embryonic lethality during organogenesis, complete penetrance J:148890
small lens J:148890
thin ventricle myocardium compact layer J:148890
Pds5aGt(RRM243)Byg/Pds5aGt(RRM243)Byg
Pds5btm1Jmi/Pds5b+
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal enteric nervous system morphology J:148890
abnormal eye development J:148890
abnormal heart morphology J:148890
abnormal interventricular septum morphology J:148890
abnormal lens development J:148890
abnormal nervous system morphology J:148890
abnormal optic vesicle formation J:148890
absent aorticopulmonary septum J:148890
common atrioventricular valve J:148890
common truncal valve J:148890
complete atrioventricular septal defect J:148890
conotruncal ridge hypoplasia J:148890
dilated heart atrium J:148890
embryonic growth retardation J:148890
embryonic lethality during organogenesis, complete penetrance J:148890
persistent truncus arteriosis J:148890
small lens J:148890
thin ventricle myocardium compact layer J:148890
Pds5aGt(RRM243)Byg/Pds5aGt(RRM243)Byg
Pds5btm1Jmi/Pds5btm1Jmi
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
embryonic lethality during organogenesis, complete penetrance J:148890
Pds5bTg(Wap-ERBB2)229Wzw/0
involves: C3H * C57BL/6
no abnormal phenotype detected J:132829

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
07/07/2020
MGI 6.15
The Jackson Laboratory