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Symbol
Name
ID

B9d1
B9 protein domain 1
MGI:1351471

Phenotype annotations related to embryo

Darker colors indicate more annotations

Human Phenotypes	Oligohydramnios
Disease(s) Associated with B9D1	Oligohydramnios
Meckel syndrome

Mouse Phenotypes		decreased embryonic cilium length	decreased embryonic cilium number	abnormal embryo development	abnormal embryonic neuroepithelium morphology
Availability	Mouse Genotype	decreased embryonic cilium length	decreased embryonic cilium number	abnormal embryo development	abnormal embryonic neuroepithelium morphology
	B9d1^{tm1a(EUCOMM)Wtsi}/B9d1^{tm1a(EUCOMM)Wtsi}
	B9d1^{tm1d(EUCOMM)Wtsi}/B9d1^{tm1d(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)
Citing These Resources Funding Information Warranty Disclaimer, Privacy Notice, Licensing, & Copyright Send questions and comments to User Support.	last database update 04/23/2024 MGI 6.23