Phenotype: abnormal placenta development

Definition
malformed or incomplete differentiation of the organ of metabolic exchange between the fetus and mother
Synonyms
abnormal placental development
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal placenta development

Total number of significant genotype-phenotype associations: 24

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center
P Value
Alg8
Alg8em1(IMPC)J
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
JAX
IMPC
0.00
Ankmy2
Ankmy2em1(IMPC)Bay
HET E12.5 abnormal placenta development Placenta Development
Gross Morphology Placenta E12.5
BCM
IMPC
0.00
Cox7c
Cox7ctm1b(KOMP)Mbp
HOM E12.5 abnormal placenta development Placenta Development
Gross Morphology Placenta E12.5
JAX
IMPC
0.00
Dbn1
Dbn1em2(IMPC)Mbp
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
UC Davis
IMPC
0.00
Folr1
Folr1tm1.1(KOMP)Vlcg
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
UC Davis
IMPC
0.00
Glmn
Glmnem1(IMPC)Bay
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
BCM
IMPC
0.00
Ints10
Ints10tm1b(KOMP)Wtsi
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
JAX
IMPC
0.00
Ipo9
Ipo9em1(IMPC)Bay
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
BCM
IMPC
0.00
Krit1
Krit1tm1.1(KOMP)Vlcg
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
UC Davis
IMPC
0.00
Mtap
Mtapem1(IMPC)Mbp
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
UC Davis
IMPC
0.00
Nr6a1
Nr6a1tm1b(EUCOMM)Wtsi
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
BCM
IMPC
0.00
Pigq
Pigqtm2b(EUCOMM)Wtsi
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
BCM
IMPC
0.00
Rad9a
Rad9atm1.1(KOMP)Wtsi
HOM E9.5 abnormal chorioallantoic fusion Chorioallantoic fusion
Gross Morphology Embryo E9.5
BCM
IMPC
0.00
Slc30a9
Slc30a9em1(IMPC)Bay
HET E12.5 abnormal placenta development Placenta Development
Gross Morphology Placenta E12.5
BCM
IMPC
0.00

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 The way we measure

 Phenotype associations stats

1.12% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal placenta development (14/1253)

1.20% females (12/1000) 1.11% males (11/992)

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