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Symbol
Name
ID
Nog
noggin
MGI:104327
Phenotype annotations related to growth/size/body
Darker colors indicate more annotations
Human Phenotypes
Inguinal hernia
Umbilical hernia
Abnormality of body height
Short stature
Disease(s) Associated with NOG
craniosynostosis
tarsal-carpal coalition syndrome

Mouse Phenotypes
abnormal secondary palate development
palatal shelf hypoplasia
short face
abnormal palatine aponeurosis morphology
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
cleft soft palate
cleft palate
abnormal snout morphology
embryonic growth retardation
decreased embryo size
slow postnatal weight gain
abnormal head morphology
decreased fetal size
Availability Mouse Genotype
Nogem1(IMPC)Mbp/Nogem1(IMPC)Mbp
Nogtm1Amc/Nogtm1Amc
Nogem1(IMPC)Mbp/Nog+
Tg(Krt14-Nog)#Jake/0
Myf5tm3(cre)Sor/Myf5+
Tg(CAG-Nog)1Ych/0  (conditional)
Osr2tm2(cre)Jian/Osr2+
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