About   Help   FAQ
Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Cecr2
CECR2, histone acetyl-lysine reader
MGI:1923799
19 phenotypes from 3 alleles in 9 genetic backgrounds
Export: Excel File
Allelic Composition
Genetic Background
Annotated Term Reference
Cecr2Gt(pGT1)1Hemc/Cecr2+
C.129P2-Cecr2Gt(pGT1)1Hemc
delayed neural tube closure J:177709
Cecr2Gt(pGT1)1Hemc/Cecr2+
involves: 129P2/OlaHsd * BALB/c
exencephaly J:96325
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
129P2(C)-Cecr2Gt(pGT1)1Hemc
exencephaly J:96325
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
C.129P2-Cecr2Gt(pGT1)1Hemc
abnormal neural tube morphology J:177709
exencephaly J:96325, J:177709
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
FVB.129P2(C)-Cecr2Gt(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
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
involves: 129P2/OlaHsd * BALB/c
absent eyelids J:96325
exencephaly J:96325
perinatal lethality, incomplete penetrance J:96325
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
involves: 129P2/OlaHsd * BALB/c * FVB/N
exencephaly J:96325
Cecr2Gt(pGT1)1Hemc/Cecr2Gt(pGT1)1Hemc
involves: C.129P2-Cecr2Gt(pGT1)1Hemc * FVB.129P2(C)-Cecr2Gt(pGT1)1Hemc
exencephaly J:96325
Cecr2tm1.1Hemc/Cecr2tm1.1Hemc
involves: BALB/c
exencephaly J:163648
Cecr2tm1.1Hemc/Cecr2tm1.1Hemc
involves: FVB/N
encephalomeningocele J:163648
exencephaly J:163648
midline facial cleft J:163648
premature death J:163648
Cecr2tm2b(EUCOMM)Hmgu/Cecr2+
C57BL/6N-Cecr2tm2b(EUCOMM)Hmgu/Tcp
abnormal embryo size J:211773
abnormal forebrain morphology J:211773
abnormal hindbrain morphology J:211773
abnormal midbrain morphology J:211773
abnormal neural tube closure J:211773
abnormal placenta size J:211773
enlarged lymph nodes J:211773
Cecr2tm2b(EUCOMM)Hmgu/Cecr2tm2b(EUCOMM)Hmgu
C57BL/6N-Cecr2tm2b(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)
Citing These Resources
Funding Information
Warranty Disclaimer & Copyright Notice
Send questions and comments to User Support.
last database update
02/11/2020
MGI 6.14
The Jackson Laboratory