|
Symbol Name ID |
Ncf1
neutrophil cytosolic factor 1 MGI:97283 |
| Darker colors indicate more annotations |
| Human Phenotypes | Sinusitis |
Malar flattening |
Clinodactyly of the 5th finger |
Hallux valgus |
Radioulnar synostosis |
Osteomyelitis |
Flexion contracture |
Joint hypermobility |
Down-sloping shoulders |
Pectus excavatum |
Kyphoscoliosis |
Osteopenia |
Osteoporosis |
| Disease(s) Associated with NCF1 | |||||||||||||
| autosomal recessive chronic granulomatous disease 1 | |||||||||||||
| chronic granulomatous disease | |||||||||||||
| Williams-Beuren syndrome |
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 04/16/2024 MGI 6.23 |
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