Coffin-Siris syndrome Gene Set

Dataset	CTD Gene-Disease Associations
Category	disease or phenotype associations
Type	disease
Description	A genetic disease that is characterized by underdevelopment of the tips of fingers or toes, underdevelopment or abscense of finger or toe nails and developmental disability. (Human Disease Ontology, DOID_1925)
External Link	http://ctdbase.org/detail.go?type=disease&acc=MESH:C536436
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Genes

6 genes/proteins associated with the disease Coffin-Siris syndrome from the curated CTD Gene-Disease Associations dataset.

Symbol	Name	Standardized Value
SMARCE1	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily e, member 1	2.88009
SMARCB1	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily b, member 1	2.88009
SMARCA2	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 2	2.88009
SMARCA4	SWI/SNF related, matrix associated, actin dependent regulator of chromatin, subfamily a, member 4	2.88009
ARID1B	AT rich interactive domain 1B (SWI1-like)	2.88009
ARID1A	AT rich interactive domain 1A (SWI-like)	2.88009