G2Cdb::Allele report

Gene	Symbol	Species	Description
G00002207	CTTN	Homo sapiens	cortactin

Disease	Description	Nervous effect
D00000220	Hearing impairment (autosomal recessive nonsyndromic)	Y

© G2C 2014. The Genes to Cognition Programme received funding from The Wellcome Trust and the EU FP7 Framework Programmes:
EUROSPIN (FP7-HEALTH-241498), SynSys (FP7-HEALTH-242167) and GENCODYS (FP7-HEALTH-241995).