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Phenotype: abnormal midbrain morphology

Definition
any structural anomaly associated with the brain region derived from the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions in the adult, including eye movement and coordination of auditory and visual reflexes
Synonyms
midbrain dysplasia,  mesencephalon dysplasia,  abnormal mesencephalon morphology
Significant gene associations The way we measure Phenotype stats
0%
of tested genes
0
significant genes
0
tested genes

IMPC Gene variants with abnormal midbrain morphology

Total number of significant genotype-phenotype associations: 17

Gene / Allele Zygosity Sex Life Stage Phenotype Parameter Phenotyping
Center		 P Value
Ambra1
Ambra1em1(IMPC)Bay 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 BCM
IMPC		 0.00
Anapc15
Anapc15tm1.1(KOMP)Vlcg 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 JAX
IMPC		 0.00
Bbox1
Bbox1tm1b(KOMP)Wtsi 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 BCM
IMPC		 0.00
Calu
Caluem1(IMPC)Tcp 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Cecr2
Cecr2tm2b(EUCOMM)Hmgu 		HET E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Cecr2
Cecr2tm2b(EUCOMM)Hmgu 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Inpp5e
Inpp5etm1.1(KOMP)Vlcg 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Laptm4b
Laptm4btm1e.1(KOMP)Wtsi 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Pygo2
Pygo2tm1b(EUCOMM)Wtsi 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Ranbp1
Ranbp1tm1b(KOMP)Wtsi 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Scrib
Scribtm1b(NCOM)Mfgc 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 TCP
IMPC		 0.00
Snx3
Snx3tm1.1(KOMP)Vlcg 		HOM E12.5 abnormal midbrain morphology Midbrain morphology
Gross Morphology Embryo E12.5		 JAX
IMPC		 0.00

Download data as:   TSV   XLS

 The way we measure

Procedure
Gross Morphology Embryo E12.5

 Phenotype associations stats

1.63% of tested genes with null mutations on a B6N genetic background have a phenotype association to abnormal midbrain morphology (11/673)

1.18% females (7/594) 1.57% males (9/575)

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