About Help FAQ

Symbol
Name
ID

B9d1
B9 protein domain 1
MGI:1351471

Phenotype annotations related to craniofacial

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
Availability	Mouse Genotype	abnormal craniofacial morphology	abnormal facial morphology	cleft palate
	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 04/16/2024 MGI 6.23