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Phenotypes associated with this allele
Allele Symbol
Allele Name
Allele ID
Cyrentm1.1(KOMP)Vlcg
targeted mutation 1.1, Velocigene
MGI:5569061
Summary 3 genotypes
Jump to Allelic Composition Genetic Background Genotype ID
hm1
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg C57BL/6N-Cyrentm1.1(KOMP)Vlcg/Ucd MGI:5797318
hm2
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg involves: C57BL/6NTac MGI:6400577
cx3
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg
Nhej1tm1Fwa/Nhej1tm1Fwa
involves: 129S6/SvEvTac * C57BL/6NTac MGI:6400579


Genotype
MGI:5797318
hm1
Allelic
Composition
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg
Genetic
Background
C57BL/6N-Cyrentm1.1(KOMP)Vlcg/Ucd
Cell Lines 12667B-H5
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cyrentm1.1(KOMP)Vlcg mutation (1 available); any Cyren mutation (9 available)
Data Sources
phenotype observed in females
phenotype observed in males
N normal phenotype
endocrine/exocrine glands
IMPC - UCD

reproductive system
IMPC - UCD




Genotype
MGI:6400577
hm2
Allelic
Composition
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg
Genetic
Background
involves: C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cyrentm1.1(KOMP)Vlcg mutation (1 available); any Cyren mutation (9 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• increased sensitivity of MEFs to infrared (IR) laser-induced DNA damage

hematopoietic system
• defects in nave splenic B cell Ig CSR in vitro
• normal development of bone marrow B cells

immune system
• defects in nave splenic B cell Ig CSR in vitro
• normal development of bone marrow B cells




Genotype
MGI:6400579
cx3
Allelic
Composition
Cyrentm1.1(KOMP)Vlcg/Cyrentm1.1(KOMP)Vlcg
Nhej1tm1Fwa/Nhej1tm1Fwa
Genetic
Background
involves: 129S6/SvEvTac * C57BL/6NTac
Find Mice Using the International Mouse Strain Resource (IMSR)
Mouse lines carrying:
Cyrentm1.1(KOMP)Vlcg mutation (1 available); any Cyren mutation (9 available)
Nhej1tm1Fwa mutation (0 available); any Nhej1 mutation (16 available)
phenotype observed in females
phenotype observed in males
N normal phenotype
cellular
• widespread neuronal apoptosis within cortex and ganglionic eminences at age E14.5-16.5

growth/size/body
• significantly reduced embryo size at age E14.5-16.5

mortality/aging
• no mice born
• significantly reduced embryo size at age E14.5-16.5
• normal Mendelian ratio at age E14.5-16.5

nervous system
• widespread neuronal apoptosis within cortex and ganglionic eminences at age E14.5-16.5





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last database update
11/19/2024
MGI 6.24
The Jackson Laboratory