Symbol Name ID |
B9d1
B9 protein domain 1 MGI:1351471 |
Darker colors indicate more annotations |
Human Phenotypes | Urethral atresia |
Dilatation of the renal pelvis |
Multicystic kidney dysplasia |
Ureteral duplication |
Disease(s) Associated with B9D1 | ||||
Joubert syndrome 27 | ||||
Meckel syndrome |
Mouse Phenotypes | abnormal renal tubule epithelial cell primary cilium morphology |
polycystic kidney |
enlarged kidney |
abnormal kidney morphology |
renal tubule hypertrophy |
dilated nephron |
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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 04/23/2024 MGI 6.23 |
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