Phenotypes Associated with This Genotype

Genotype
MGI:5767605

• Allelic Composition: Cnnm2^{tm1.1(KOMP)Vlcg}/Cnnm2^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Cnnm2^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 14695A-D6

Data Sources

IMPC Data for Cnnm2

• ♀: phenotype observed in females
• ♂: phenotype observed in males
• N: normal phenotype

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

craniofacial

abnormal craniofacial morphology ( J:211773 )

♂

IMPC - UCD

abnormal head shape ( J:211773 )

IMPC - UCD

embryo

embryonic growth retardation ( J:211773 )

♂

IMPC - UCD

spina bifida ( J:211773 )

IMPC - UCD

growth/size/body

abnormal head shape ( J:211773 )

IMPC - UCD

embryonic growth retardation ( J:211773 )

♂

IMPC - UCD

abnormal head size ( J:211773 )

IMPC - UCD

microcephaly ( J:211773 )

IMPC - UCD

limbs/digits/tail

polydactyly ( J:211773 )

IMPC - UCD

syndactyly ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

vision/eye

microphthalmia ( J:211773 )

IMPC - UCD

anophthalmia ( J:211773 )

IMPC - UCD