69 phenotypes from multigenic genotypes

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