Phenotypes Associated with This Genotype

Genotype
MGI:4455029

cx2

• Allelic Composition: Mitf^mi-ew/Mitf^mi-ew; Tfe3^tm1Est/Tfe3⁺
• Genetic Background: either: (involves: 129/Sv * 129S1/Sv * C57BL/6Bn * NAW) or (involves: 129S1/Sv * C57BL/6Bn * C57BL/6J * NAW)

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

pigmentation

absent coat pigmentation ( J:89821 )

♀ • white coat

skeleton

osteopetrosis ( J:89821 )

♀ • osteopetrosis is more severe than in Mitf^mi-ew homozygotes but less severe than in double homozygotes

vision/eye

microphthalmia ( J:89821 )

♀

integument

absent coat pigmentation ( J:89821 )

♀ • white coat