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Symbol
Name
ID
Cdkn1c
cyclin-dependent kinase inhibitor 1C (P57)
MGI:104564
Phenotype annotations related to behavior/neurological
Darker colors indicate more annotations
Human Phenotypes
Feeding difficulties in infancy
Sleep apnea
Disease(s) Associated with CDKN1C
Beckwith-Wiedemann syndrome

Mouse Phenotypes
absent gastric milk in neonates
dysphagia
abnormal suckling behavior
Availability Mouse Genotype
Cdkn1ctm1Bbd/Cdkn1ctm1Bbd
Cdkn1ctm1Kat/Cdkn1ctm1Kat
Cdkn1ctm1Bbd/Cdkn1c+
Cdkn1ctm1Kat/Cdkn1c+

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
09/18/2018
MGI 6.12
The Jackson Laboratory