Phenotypes associated with this allele

• Allele Symbol: Ovol1^{tm1b(KOMP)Wtsi}
• Allele Name: targeted mutation 1b, Wellcome Trust Sanger Institute
• Allele ID: MGI:5507829
• Summary: 1 genotype

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Ovol1^tm1b(KOMP)Wtsi/Ovol1^+	C57BL/6N-Ovol1^tm1b(KOMP)Wtsi/J	MGI:5631375

Genotype
MGI:5631375

ht1

• Allelic Composition: Ovol1^{tm1b(KOMP)Wtsi}/Ovol1⁺
• Genetic Background: C57BL/6N-Ovol1^{tm1b(KOMP)Wtsi}/J
• Cell Lines: EPD0570_3_D10

Data Sources

IMPC Data for Ovol1

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

hematopoietic system

decreased erythrocyte cell number ( J:211773 )

♀

IMPC - JAX

decreased hematocrit ( J:211773 )

♀

IMPC - JAX

decreased hemoglobin content ( J:211773 )

♀

IMPC - JAX

thrombocytopenia ( J:211773 )

♀

IMPC - JAX

integument

abnormal coat/hair pigmentation ( J:211773 )

IMPC - JAX

abnormal vibrissa morphology ( J:211773 )

♀

IMPC - JAX

pigmentation

abnormal coat/hair pigmentation ( J:211773 )

IMPC - JAX