Ccnd2 Phenotype Annotations - Multigenic Genotypes

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Ccnd2
cyclin D2
MGI:88314

25 phenotypes from multigenic genotypes

Allelic Composition Genetic Background	Annotated Term	Reference
Ccnd1^tm1Dsn/Ccnd1^tm1Dsn Ccnd2^tm1Wbg/Ccnd2^tm1Wbg Ccnd3^tm1Pisc/Ccnd3^tm1Pisc involves: 129P2/OlaHsd * 129S2/SvPas	abnormal common myeloid progenitor cell morphology	J:92563
	abnormal definitive hematopoiesis	J:92563
	abnormal hematopoietic stem cell morphology	J:92563
	abnormal interventricular septum morphology	J:92563
	abnormal lymphopoiesis	J:92563
	anemia	J:92563
	decreased erythrocyte cell number	J:92563
	decreased hematopoietic stem cell number	J:92563
	hydrops fetalis	J:92563
	lethality throughout fetal growth and development, complete penetrance	J:92563
	thin ventricular wall	J:92563
Ccnd1^tm1Phin/Ccnd1^tm1Phin Ccnd2^tm1Wbg/Ccnd2^tm1Wbg involves: 129S2/SvPas * 129S4/SvJae * C57BL/6	abnormal cerebellum development	J:105045
Ccnd1^tm1Wbg/Ccnd1^tm1Wbg Ccnd2^tm1Wbg/Ccnd2^tm1Wbg Not Specified	abnormal cerebellar granule layer morphology	J:80994
	absent Purkinje cell layer	J:80994
	ectopic Purkinje cell	J:80994
	impaired coordination	J:80994
	postnatal lethality	J:80994
	reduced cerebellar foliation	J:80994
	retina hypoplasia	J:80994
	small cerebellum	J:80994
Ccnd2^tm1Wbg/Ccnd2^tm1Wbg Ccnd3^tm1Pisc/Ccnd3^tm1Pisc Not Specified	abnormal erythropoiesis	J:80994
	abnormal liver development	J:80994
	lethality throughout fetal growth and development, complete penetrance	J:80994
	low mean erythrocyte cell number	J:80994
	macrocytic anemia	J:80994
	macrocytosis	J:80994

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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