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Symbol
Name
ID
Nog
noggin
MGI:104327
Phenotype annotations related to muscle
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
Availability Mouse Genotype
Nogtm1Amc/Nogtm1Amc
Myf5tm3(cre)Sor/Myf5+
Tg(CAG-Nog)1Ych/0  (conditional)
Osr2tm5(cre)Jian/Osr2+
Tg(CAG-Nog)1Ych/0  (conditional)

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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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory