About Help FAQ

Symbol
Name
ID

Smarca4
SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4
MGI:88192

Phenotype annotations related to limbs/digits/tail

Darker colors indicate more annotations

Human Phenotypes	Short 5th finger	Prominent interphalangeal joints	Short phalanx of the 5th toe
Disease(s) Associated with SMARCA4
Coffin-Siris syndrome 4

Mouse Phenotypes		abnormal apical ectodermal ridge morphology	abnormal digit morphology	monodactyly	abnormal hindlimb morphology	abnormal hindlimb zeugopod morphology
Availability	Mouse Genotype	abnormal apical ectodermal ridge morphology	abnormal digit morphology	monodactyly	abnormal hindlimb morphology	abnormal hindlimb zeugopod morphology
	Smarca4^tm1.2Pcn/Smarca4^tm1.2Pcn Tg(KRT14-cre)1Ipc/? (conditional)
	Smarca4^tm1.2Pcn/Smarca4^tm1.2Pcn Tg(KRT14-cre/ERT2)1Ipc/? (conditional)

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 04/30/2024 MGI 6.23