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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Cdkn1c
cyclin dependent kinase inhibitor 1C
MGI:104564
69 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Cdkn1atm1Led/Cdkn1atm1Led
Cdkn1ctm1Sje/Cdkn1c+
involves: 129S6/SvEvTac * 129S7/SvEvBrd * C57BL/6 		abnormal axial skeleton morphology J:52552
abnormal bronchiole morphology J:52552
abnormal bronchus morphology J:52552
abnormal ileum morphology J:52552
abnormal jejunum morphology J:52552
abnormal kidney medulla development J:52552
abnormal lens development J:52552
abnormal lens epithelium morphology J:52552
abnormal limb bone morphology J:52552
abnormal long bone epiphysis morphology J:52552
abnormal pulmonary alveolus morphology J:52552
abnormal rib morphology J:52552
abnormal spine curvature J:52552
abnormal sternocostal joint morphology J:52552
abnormal sternum morphology J:52552
cleft palate J:52552
decreased fetal size J:52552
decreased skeletal muscle mass J:52552
herniated abdominal wall J:52552
increased skeletal muscle fiber size J:52552
lethality throughout fetal growth and development, incomplete penetrance J:52552
omphalocele J:52552
perinatal lethality, complete penetrance J:52552
postnatal lethality J:52552
respiratory distress J:52552
rib bifurcation J:52552
short sternum J:52552
small inner medullary pyramid J:52552
split sternum J:52552
thin diaphragm muscle J:52552
Cdkn1atm1Led/Cdkn1atm1Led
Cdkn1ctm2.1Kei/Cdkn1c+
Tg(Mx1-cre)1Cgn/0
B6.Cg-Cdkn1ctm2.1Kei Cdkn1atm1Led Tg(Mx1-cre)1Cgn 		abnormal hematopoietic stem cell physiology J:176209
Cdkn1ctm1.1(Cdkn1b*)Kei/Cdkn1c+
B6.129P2-Cdkn1ctm1.1(Cdkn1b*)Kei 		normal hematopoietic system phenotype J:176209
Cdkn1ctm1.1(Cdkn1b*)Kei/Cdkn1c+
involves: 129P2/OlaHsd * C57BL/6J 		abnormal abdominal wall morphology J:147145
abnormal kidney papilla morphology J:147145
abnormal placenta morphology J:147145
normal digestive/alimentary phenotype J:147145
enlarged adrenal glands J:147145
normal growth/size/body region phenotype J:147145
normal mortality/aging J:147145
omphalocele J:147145
paternal imprinting J:147145
normal skeleton phenotype J:147145
uterus atresia J:147145
uterus atrophy J:147145
normal vision/eye phenotype J:147145
Cdkn1ctm1Sje/Cdkn1c+
Kcnq1ot1tm1Tilg/Kcnq1ot1+
involves: 129 * C57BL/6 		abnormal imprinting J:108700
normal mortality/aging J:108700
Tg(BAC144D14)5A2Masu/0
B6J.Cg-Tg(BAC144D14)5A2Masu 		abnormal interscapular fat pad morphology J:232408
abnormal retroperitoneal fat pad morphology J:232408
abnormal white adipose tissue morphology J:232408
decreased birth weight J:232408
decreased body weight J:232408
decreased fetal weight J:232408
decreased food intake J:232408
decreased inguinal fat pad weight J:232408
decreased mesenteric fat pad weight J:232408
decreased retroperitoneal fat pad weight J:232408
hypoglycemia J:232408
increased body temperature J:232408
increased brain weight J:232408
increased brown adipose tissue amount J:232408
increased brown fat cell number J:232408
increased interscapular fat pad weight J:232408
Tg(BAC144D14)5D3Masu/0
B6.Cg-Tg(BAC144D14)5D3Masu 		abnormal hypothalamus morphology J:239325
abnormal sucrose solution preference J:239325
decreased locomotor activity J:239325
decreased prepulse inhibition J:239325
impaired hearing J:239325
reduced sensorimotor gating J:239325
Tg(BAC144D14)5D3Masu/0
B6J.Cg-Tg(BAC144D14)5D3Masu 		abnormal beige fat cell morphology J:232408
abnormal interscapular fat pad morphology J:232408
abnormal retroperitoneal fat pad morphology J:232408
abnormal white adipose tissue morphology J:232408
decreased birth weight J:232408
decreased body weight J:232408
decreased fetal weight J:232408
decreased inguinal fat pad weight J:232408
decreased mesenteric fat pad weight J:232408
decreased retroperitoneal fat pad weight J:232408
hypoglycemia J:232408
increased body temperature J:232408
increased brown adipose tissue amount J:232408
increased brown fat cell number J:232408
increased interscapular fat pad weight J:232408
Tg(YACW408A5)1952Ricc/0
involves: 129/Sv * SD7 		abnormal imprinting J:96366
fetal growth retardation J:96366
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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Send questions and comments to User Support. 		last database update
10/29/2024
MGI 6.24 		The Jackson Laboratory