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Symbol
Name
ID

Arid1b
AT-rich interaction domain 1B
MGI:1926129

Phenotype annotations related to muscle

Darker colors indicate more annotations

Human Phenotypes	Congenital diaphragmatic hernia	Hypotonia	Infantile muscular hypotonia
Disease(s) Associated with ARID1B	Congenital diaphragmatic hernia	Hypotonia	Infantile muscular hypotonia
Coffin-Siris syndrome
Coffin-Siris syndrome 1

Mouse Phenotypes		muscle weakness
Availability	Mouse Genotype	muscle weakness
	Arid1b^em1Hzhu/Arid1b⁺

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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