About Help FAQ

Symbol
Name
ID

Deaf1
DEAF1, transcription factor
MGI:1858496

Phenotype annotations related to skeleton

Darker colors indicate more annotations

Human Phenotypes	Frontal bossing	Brachycephaly	Mandibular prognathia	Prominent fingertip pads	2-3 toe cutaneous syndactyly	Sacral dimple	Joint hypermobility
Disease(s) Associated with DEAF1
Vulto-van Silfout-de Vries syndrome

Mouse Phenotypes		abnormal sternocostal joint morphology	rib bifurcation	rib fusion	cervical vertebral fusion
Availability	Mouse Genotype	abnormal sternocostal joint morphology	rib bifurcation	rib fusion	cervical vertebral fusion
	Deaf1^tm1Sho/Deaf1^tm1Sho
	Deaf1^tm1Sho/Deaf1⁺

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