Phenotypes associated with this allele

• Allele Symbol: Cep97^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5708221
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Cep97^tm1.1(KOMP)Vlcg/Cep97^tm1.1(KOMP)Vlcg	C57BL/6N-Cep97^tm1.1(KOMP)Vlcg/Ucd	MGI:5767598
ht2	Cep97^tm1.1(KOMP)Vlcg/Cep97^+	C57BL/6N-Cep97^tm1.1(KOMP)Vlcg/Ucd	MGI:6678673

Genotype
MGI:5767598

hm1

• Allelic Composition: Cep97^{tm1.1(KOMP)Vlcg}/Cep97^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Cep97^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 13424B-H1

Data Sources

IMPC Data for Cep97

• ♀: 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

cleft palate ( J:211773 )

IMPC - UCD

digestive/alimentary system

cleft palate ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

growth/size/body

cleft palate ( J:211773 )

IMPC - UCD

homeostasis/metabolism

edema ( J:211773 )

IMPC - UCD

integument

bleb ( 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

Genotype
MGI:6678673

ht2

• Allelic Composition: Cep97^{tm1.1(KOMP)Vlcg}/Cep97⁺
• Genetic Background: C57BL/6N-Cep97^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 13424B-H1

Data Sources

IMPC Data for Cep97

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD