Phenotypes associated with this allele

• Allele Symbol: Ywhab^{tm1b(EUCOMM)Hmgu}
• Allele Name: targeted mutation 1b, Helmholtz Zentrum Muenchen GmbH
• Allele ID: MGI:6161255
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
hm1	Ywhab^tm1b(EUCOMM)Hmgu/Ywhab^tm1b(EUCOMM)Hmgu	C57BL/6N-Ywhab^tm1b(EUCOMM)Hmgu/Ieg	MGI:6408767

Genotype
MGI:6408767

hm1

• Allelic Composition: Ywhab^{tm1b(EUCOMM)Hmgu}/Ywhab^{tm1b(EUCOMM)Hmgu}
• Genetic Background: C57BL/6N-Ywhab^{tm1b(EUCOMM)Hmgu}/Ieg
• Cell Lines: HEPD0510_2_A07

Data Sources

IMPC Data for Ywhab

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

behavior/neurological

abnormal behavior ( J:211773 )

♂

IMPC - HMGU

hematopoietic system

thrombocytopenia ( J:211773 )

♂

IMPC - HMGU

homeostasis/metabolism

decreased blood urea nitrogen level ( J:211773 )

♂

IMPC - HMGU

increased circulating bilirubin level ( J:211773 )

♂

IMPC - HMGU

decreased circulating glucose level ( J:211773 )

♂

IMPC - HMGU

decreased circulating cholesterol level ( J:211773 )

♂

IMPC - HMGU

decreased circulating HDL cholesterol level ( J:211773 )

♂

IMPC - HMGU

decreased circulating triglyceride level ( J:211773 )

♂

IMPC - HMGU

decreased circulating iron level ( J:211773 )

♂

IMPC - HMGU

decreased circulating total protein level ( J:211773 )

♂

IMPC - HMGU

vision/eye

abnormal retina morphology ( J:211773 )

IMPC - HMGU

decreased total retina thickness ( J:211773 )

IMPC - HMGU