Phenotypes associated with this allele

• Allele Symbol: Kbtbd7^{tm1.1(KOMP)Vlcg}
• Allele Name: targeted mutation 1.1, Velocigene
• Allele ID: MGI:5635225
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Kbtbd7^tm1.1(KOMP)Vlcg/Kbtbd7^tm1.1(KOMP)Vlcg	C57BL/6N-Kbtbd7^tm1.1(KOMP)Vlcg/J	MGI:6262728

Genotype
MGI:6262728

hm1

• Allelic Composition: Kbtbd7^{tm1.1(KOMP)Vlcg}/Kbtbd7^{tm1.1(KOMP)Vlcg}
• Genetic Background: C57BL/6N-Kbtbd7^{tm1.1(KOMP)Vlcg}/J
• Cell Lines: 10920A-E3

Data Sources

IMPC Data for Kbtbd7

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

behavior/neurological

abnormal behavior ( J:211773 )

IMPC - JAX

decreased thigmotaxis ( J:211773 )

IMPC - JAX

decreased grip strength ( J:211773 )

IMPC - JAX

hyperactivity ( J:211773 )

IMPC - JAX

homeostasis/metabolism

increased circulating bilirubin level ( J:211773 )

♀

IMPC - JAX

skeleton

abnormal bone structure ( J:211773 )

♀

IMPC - JAX

decreased bone mineral content ( J:211773 )

♀

IMPC - JAX