Phenotypes associated with this allele

• Allele Symbol: Wbp1l^{tm2b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 2b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:5692573
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Wbp1l^tm2b(EUCOMM)Hmgu/Wbp1l^tm2b(EUCOMM)Hmgu	C57BL/6N-Wbp1l^tm2b(EUCOMM)Hmgu/Bay	MGI:6288823

Genotype
MGI:6288823

hm1

• Allelic Composition: Wbp1l^{tm2b(EUCOMM)Hmgu}/Wbp1l^{tm2b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Wbp1l^{tm2b(EUCOMM)Hmgu}/Bay
• Cell Lines: HEPD0797_6_B06

Data Sources

IMPC Data for Wbp1l

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

behavior/neurological

increased startle reflex ( J:211773 )

IMPC - BCM

hyperactivity ( J:211773 )

♀

IMPC - BCM

cardiovascular system

decreased heart rate ( J:211773 )

♀

IMPC - BCM

prolonged RR interval ( J:211773 )

♀

IMPC - BCM

prolonged ST segment ( J:211773 )

♀

IMPC - BCM

homeostasis/metabolism

decreased circulating calcium level ( J:211773 )

IMPC - BCM

decreased circulating alkaline phosphatase level ( J:211773 )

IMPC - BCM

decreased circulating serum albumin level ( J:211773 )

IMPC - BCM

decreased circulating total protein level ( J:211773 )

IMPC - BCM

integument

abnormal skin coloration ( J:211773 )

♀

IMPC - BCM

nervous system

decreased prepulse inhibition ( J:211773 )

IMPC - BCM

vision/eye

abnormal eye anterior chamber depth ( J:211773 )

♀

IMPC - BCM