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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Ccm2l
cerebral cavernous malformation 2-like
MGI:2385159
9 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background		 Annotated Term Reference
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn
Ccm2Gt(RRG051)Byg/Ccm2+
involves: 129 * 129P2/OlaHsd * C57BL/6 		no abnormal phenotype detected J:187714
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn
Ccm2Gt(RRG051)Byg/Ccm2+
Heg1tm1Mlkn/Heg1tm1Mlkn
involves: 129 * 129P2/OlaHsd * C57BL/6 		abnormal cardiovascular development J:187714
prenatal lethality, incomplete penetrance J:187714
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn
Ccm2tm1Mlkn/Ccm2+
Heg1tm1Mlkn/Heg1tm2.1Mlkn
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * SJL 		prenatal lethality, incomplete penetrance J:187714
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn
Heg1tm1Mlkn/Heg1tm1Mlkn
involves: 129 * C57BL/6 		decreased fetal cardiomyocyte proliferation J:187714
decreased ventricle muscle contractility J:187714
dilated heart atrium J:187714
embryonic lethality during organogenesis, complete penetrance J:187714
thin myocardium J:187714
trabecula carnea hypoplasia J:187714
Ccm2ltm1Mlkn/Ccm2ltm1Mlkn
Heg1tm1Mlkn/Heg1tm2.1Mlkn
Tg(Tek-cre)1Ywa/0
involves: 129 * C57BL/6 * SJL 		embryonic lethality during organogenesis, complete penetrance J:187714
thin myocardium J:187714
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
04/16/2024
MGI 6.23 		The Jackson Laboratory