Symbol Name ID |
Nog
noggin MGI:104327 |
Darker colors indicate more annotations |
Human Phenotypes | Camptodactyly of finger |
Joint contracture of the hand |
Camptodactyly |
Rigidity |
Hypotonia |
Generalized hypotonia |
Abdominal wall muscle weakness |
Disease(s) Associated with NOG | |||||||
craniosynostosis | |||||||
Huntington's disease | |||||||
proximal symphalangism |
Mouse Phenotypes | abnormal soft palate muscle morphology |
abnormal levator veli palatini muscle morphology |
small levator veli palatini muscle |
abnormal palatopharyngeus muscle morphology |
abnormal tensor veli palatini muscle morphology |
small tensor veli palatini muscle |
abnormal muscle morphology |
abnormal muscle fiber morphology |
abnormal superior pharyngeal constrictor muscle morphology |
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Availability | Mouse Genotype | |||||||||
Nogtm1Amc/Nogtm1Amc | ||||||||||
Myf5tm3(cre)Sor/Myf5+ Tg(CAG-Nog)1Ych/0 (conditional) |
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Osr2tm5(cre)Jian/Osr2+ Tg(CAG-Nog)1Ych/0 (conditional) |
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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