Phenotypes associated with this allele

• Allele Symbol: Ovol1⁺
• Allele Name: wild type
• Allele ID: MGI:2441272
• Summary: 2 genotypes

Jump to	Allelic Composition	Genetic Background	Genotype ID
ht1	Ovol1^tm1Efu/Ovol1^+	B6.129-Ovol1^tm1Efu	MGI:3815071
ht2	Ovol1^tm1b(KOMP)Wtsi/Ovol1^+	C57BL/6N-Ovol1^tm1b(KOMP)Wtsi/J	MGI:5631375

Genotype
MGI:3815071

ht1

• Allelic Composition: Ovol1^tm1Efu/Ovol1⁺
• Genetic Background: B6.129-Ovol1^tm1Efu

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

renal/urinary system

kidney cyst ( J:118154 )

• on a congenic B6 background, only 1 of ~40 adult heterozygotes display a unilateral cystic kidney, in the absence of kidney developmental defects

growth/size/body

kidney cyst ( J:118154 )

• on a congenic B6 background, only 1 of ~40 adult heterozygotes display a unilateral cystic kidney, in the absence of kidney developmental defects

Genotype
MGI:5631375

ht2

• 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

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