Phenotypes associated with this allele

• Allele Symbol: Cnnm2^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5692792
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cnnm2^tm1.1(KOMP)Vlcg/Cnnm2^tm1.1(KOMP)Vlcg	C57BL/6N-Cnnm2^tm1.1(KOMP)Vlcg/Ucd	MGI:5767605
ht2	Cnnm2^tm1.1(KOMP)Vlcg/Cnnm2^+	C57BL/6N-Cnnm2^tm1.1(KOMP)Vlcg/Ucd	MGI:6262175

Genotype
MGI:5767605

hm1

• 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 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

homeostasis/metabolism

edema ( J:211773 )

IMPC - UCD

mortality/aging

preweaning lethality, complete penetrance ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

exencephaly ( J:211773 )

IMPC - UCD

vision/eye

microphthalmia ( J:211773 )

IMPC - UCD

Genotype
MGI:6262175

ht2

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

Data Sources

IMPC Data for Cnnm2

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD

skeleton

increased bone mineral density ( J:211773 )

♀

IMPC - UCD