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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	Camptodactyly of finger	Tapered finger	Cutaneous syndactyly of toes	Clubbing	Flexion contracture of digit
Disease(s) Associated with SMARCAD1	Camptodactyly of finger	Tapered finger	Cutaneous syndactyly of toes	Clubbing	Flexion contracture of digit
adermatoglyphia
BASAN syndrome

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	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
	Smarcad1^tm1Gos/Smarcad1^tm1Gos					!
	Smarcad1^tm1Gos/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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