Cecr2 Phenotype Annotations

Mammalian Phenotype Ontology Annotations
Query Results - Summary

Symbol
Name
ID

Cecr2
CECR2, histone acetyl-lysine reader
MGI:1923799

20 phenotypes from 3 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Cecr2^{Gt(pGT1)1Hemc}/Cecr2⁺ C.129P2-Cecr2^{Gt(pGT1)1Hemc}	delayed neural tube closure	J:177709
Cecr2^{Gt(pGT1)1Hemc}/Cecr2⁺ involves: 129P2/OlaHsd * BALB/c	exencephaly	J:96325
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} 129P2(C)-Cecr2^{Gt(pGT1)1Hemc}	exencephaly	J:96325
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} C.129P2-Cecr2^{Gt(pGT1)1Hemc}	abnormal neural tube morphology	J:177709
	exencephaly	J:96325, J:177709
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} FVB.129P2(C)-Cecr2^{Gt(pGT1)1Hemc}	abnormal neural tube morphology	J:177709
	delayed neural tube closure	J:177709
	exencephaly	J:177709
	normal hearing/vestibular/ear phenotype	J:177709
	normal nervous system phenotype	J:96325
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} involves: 129P2/OlaHsd * BALB/c	absent eyelids	J:96325
	exencephaly	J:96325
	perinatal lethality, incomplete penetrance	J:96325
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} involves: 129P2/OlaHsd * BALB/c * FVB/N	exencephaly	J:96325
Cecr2^{Gt(pGT1)1Hemc}/Cecr2^{Gt(pGT1)1Hemc} involves: C.129P2-Cecr2^{Gt(pGT1)1Hemc} * FVB.129P2(C)-Cecr2^{Gt(pGT1)1Hemc}	exencephaly	J:96325
Cecr2^tm1.1Hemc/Cecr2^tm1.1Hemc involves: 129S6/SvEvTac * BALB/c * C57BL/6NTac	exencephaly	J:163648
Cecr2^tm1.1Hemc/Cecr2^tm1.1Hemc involves: 129S6/SvEvTac * C57BL/6NTac * FVB/N	encephalomeningocele	J:163648
	exencephaly	J:163648
	midline facial cleft	J:163648
	premature death	J:163648
Cecr2^{tm2b(EUCOMM)Hmgu}/Cecr2⁺ C57BL/6N-Cecr2^{tm2b(EUCOMM)Hmgu}/Tcp	abnormal forebrain morphology	J:211773
	abnormal hindbrain morphology	J:211773
	abnormal midbrain morphology	J:211773
	abnormal neural tube closure	J:211773
	abnormal QT variability	J:211773
	decreased exploration in new environment	J:211773
	enlarged lymph nodes	J:211773
	increased circulating alkaline phosphatase level	J:211773
Cecr2^{tm2b(EUCOMM)Hmgu}/Cecr2^{tm2b(EUCOMM)Hmgu} C57BL/6N-Cecr2^{tm2b(EUCOMM)Hmgu}/Tcp	abnormal craniofacial morphology	J:211773
	abnormal forebrain morphology	J:211773
	abnormal hindbrain morphology	J:211773
	abnormal midbrain morphology	J:211773
	abnormal neural tube closure	J:211773
	preweaning lethality, complete penetrance	J:211773

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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