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Symbol
Name
ID
B9d1
B9 protein domain 1
MGI:1351471
Phenotype annotations related to vision/eye
Darker colors indicate more annotations
Human Phenotypes
Nystagmus
Oculomotor apraxia
Disease(s) Associated with B9D1
Joubert syndrome 27

Mouse Phenotypes
microphthalmia
Availability Mouse Genotype
B9d1tm1a(EUCOMM)Wtsi/B9d1tm1a(EUCOMM)Wtsi
B9d1tm1d(EUCOMM)Wtsi/B9d1tm1d(EUCOMM)Wtsi

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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Funding Information
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last database update
10/08/2019
MGI 6.14
The Jackson Laboratory