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Symbol
Name
ID

Ncf1
neutrophil cytosolic factor 1
MGI:97283

Phenotype annotations related to behavior/neurological

Darker colors indicate more annotations

Human Phenotypes	Feeding difficulties in infancy	Vocal cord paralysis	Atypical behavior	Obsessive-compulsive trait	Attention deficit hyperactivity disorder	Hyperacusis	Phonophobia	Hoarse voice
Disease(s) Associated with NCF1
Williams-Beuren syndrome

Mouse Phenotypes		abnormal behavior	impaired cued conditioning behavior	abnormal spatial learning	decreased anxiety-related response	decreased thigmotaxis	abnormal locomotor activation	decreased locomotor activity
Availability	Mouse Genotype	abnormal behavior	impaired cued conditioning behavior	abnormal spatial learning	decreased anxiety-related response	decreased thigmotaxis	abnormal locomotor activation	decreased locomotor activity
	Ncf1^em1(IMPC)Mbp/Ncf1^em1(IMPC)Mbp
	Ncf1^tm1Shl/Ncf1^tm1Shl

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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