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Symbol
Name
ID
Smarcad1
SWI/SNF-related, matrix-associated actin-dependent regulator of chromatin, subfamily a, containing DEAD/H box 1
MGI:95453
Phenotype annotations related to skeleton
!Indicates phenotype varies with strain background.
Darker colors indicate more annotations
Human Phenotypes
Clubbing
Disease(s) Associated with SMARCAD1
adermatoglyphia

Mouse Phenotypes
abnormal sternocostal joint morphology
asymmetric sternocostal joints
split xiphoid process
short sternum
abnormal axial skeleton morphology
rib fusion
abnormal thoracic vertebrae morphology
small thoracic cage
abnormal spine curvature
lumbar vertebral fusion
Availability Mouse Genotype
Smarcad1tm1Gos/Smarcad1tm1Gos !
Smarcad1tm1Gos/Smarcad1+ !

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)
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last database update
01/14/2020
MGI 6.14
The Jackson Laboratory