|
Symbol Name ID |
Ncf1
neutrophil cytosolic factor 1 MGI:97283 |
| Darker colors indicate more annotations |
| Human Phenotypes | Stroke |
Meningitis |
Cerebellar hypoplasia |
Chiari type I malformation |
Incoordination |
Poor coordination |
Vocal cord paralysis |
Anxiety |
Atypical behavior |
Obsessive-compulsive trait |
Attention deficit hyperactivity disorder |
Hyperacusis |
Phonophobia |
Short attention span |
Intellectual disability |
Sleep abnormality |
Hyperreflexia |
Gait imbalance |
Impaired visuospatial constructive cognition |
| Disease(s) Associated with NCF1 | |||||||||||||||||||
| chronic granulomatous disease | |||||||||||||||||||
| Williams-Beuren syndrome |
| Mouse Phenotypes | enhanced long-term potentiation |
reduced long-term potentiation |
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| Availability | Mouse Genotype | ||
| Ncf1tm1Shl/Ncf1tm1Shl | |||
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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last database update 05/28/2024 MGI 6.13 |
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