Phenotypes associated with this allele

• Allele Symbol: Krt14^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5708279
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Krt14^tm1.1(KOMP)Vlcg/Krt14^tm1.1(KOMP)Vlcg	C57BL/6N-Krt14^tm1.1(KOMP)Vlcg/Ucd	MGI:6262768
ht2	Krt14^tm1.1(KOMP)Vlcg/Krt14^+	C57BL/6N-Krt14^tm1.1(KOMP)Vlcg/Ucd	MGI:6678934

Genotype
MGI:6262768

hm1

• Allelic Composition: Krt14^{tm1.1(KOMP)Vlcg}/Krt14^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Krt14^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 12488A-C5

Data Sources

IMPC Data for Krt14

• ♀: 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

embryonic growth retardation ( J:211773 )

IMPC - UCD

spina bifida ( J:211773 )

IMPC - UCD

growth/size/body

cleft palate ( J:211773 )

IMPC - UCD

embryonic growth retardation ( 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:6678934

ht2

• Allelic Composition: Krt14^{tm1.1(KOMP)Vlcg}/Krt14⁺
• Genetic Background: C57BL/6N-Krt14^{tm1.1(KOMP)Vlcg}/Ucd
• Cell Lines: 12488A-C5

Data Sources

IMPC Data for Krt14

cardiovascular system

hemorrhage ( J:211773 )

IMPC - UCD

embryo

spina bifida ( J:211773 )

IMPC - UCD

nervous system

spina bifida ( J:211773 )

IMPC - UCD