Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
Darker colors indicate more annotations |
Human Phenotypes | Frontal bossing |
Micrognathia |
Dandy-Walker malformation |
Microcephaly |
Encephalocele |
Triangular face |
Full cheeks |
Sloping forehead |
Thick lower lip vermilion |
Cleft palate |
Aplasia/Hypoplasia of the tongue |
Furrowed tongue |
Depressed nasal ridge |
Disease(s) Associated with B9D1 | |||||||||||||
Joubert syndrome 27 | |||||||||||||
Meckel syndrome |
Mouse Phenotypes | abnormal craniofacial morphology |
abnormal facial morphology |
cleft palate |
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Availability | Mouse Genotype | |||
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi | ||||
B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)Wtsi |
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 05/28/2024 MGI 6.13 |
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