Phenotype: facial cleft

Definition
a cleft resulting from incomplete merging or fusion of any of the embryonic facial processes that normally unite to form the face
Synonyms
split-face malformation,  prosopoanoschisis,  split face malformation
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with facial cleft

Total number of significant genotype-phenotype associations: 38

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center
P Value
Ambra1
Ambra1em1(IMPC)Bay
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
BCM
IMPC
0.00
Amt
Amtem1(IMPC)Tcp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
TCP
IMPC
0.00
Cdk20
Cdk20em1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Cep135
Cep135em1(IMPC)J
HOM E12.5 facial cleft Facial cleft
Gross Morphology Embryo E12.5
JAX
IMPC
0.00
Esrp1
Esrp1em1(IMPC)Mbp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
UC Davis
IMPC
0.00
Fuz
Fuzem1(IMPC)Mbp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
UC Davis
IMPC
0.00
Gnb1
Gnb1em1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Hesx1
Hesx1em1(IMPC)J
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
JAX
IMPC
0.00
Mllt10
Mllt10em1(IMPC)Mbp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
UC Davis
IMPC
0.00
Mmachc
Mmachctm1.1(NCOM)Mfgc
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
TCP
IMPC
0.00
Nxn
Nxnem1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Nxn
Nxnem1(IMPC)J
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
JAX
IMPC
0.00
Nxn
Nxntm1b(EUCOMM)Wtsi
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Pax6
Pax6em1(IMPC)Mbp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
UC Davis
IMPC
0.00
Pcgf3
Pcgf3em1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Pign
Pignem1(IMPC)Mbp
HOM E15.5 facial cleft Facial Cleft
Gross Morphology Embryo E14.5-E15.5
UC Davis
IMPC
0.00
Ptov1
Ptov1em1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Rab34
Rab34tm1b(EUCOMM)Hmgu
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
JAX
IMPC
0.00
Shroom3
Shroom3em1(IMPC)Bay
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
BCM
IMPC
0.00
Slc25a1
Slc25a1tm1b(EUCOMM)Wtsi
HOM E12.5 facial cleft Facial cleft
Gross Morphology Embryo E12.5
BCM
IMPC
0.00
Tbc1d32
Tbc1d32em1(IMPC)J
HOM E18.5 facial cleft Facial Cleft
Gross Morphology Embryo E18.5
JAX
IMPC
0.00
Togaram1
Togaram1em1(IMPC)J
HOM E12.5 facial cleft Facial cleft
Gross Morphology Embryo E12.5
JAX
IMPC
0.00

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 The way we measure

 Phenotype associations stats

2.22% of tested genes with null mutations on a B6N genetic background have a phenotype association to facial cleft (20/899)

3.05% females (17/557) 3.31% males (18/543)

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