Phenotypes Associated with This Genotype

Genotype
MGI:3707222

• Allelic Composition: Hectd1^Gt(XC266)Byg/Hectd1^Gt(XC266)Byg
• Genetic Background: involves: 129P2/OlaHsd

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

craniofacial

abnormal neurocranium morphology ( J:122594 )

• authors state that the phenotype observed is identical to that of Hectd1^opm homozygotes

absent temporal bone petrous part ( J:122594 )

abnormal frontal bone morphology ( J:122594 )

absent interparietal bone ( J:122594 )

absent exoccipital bone ( J:122594 )

abnormal parietal bone morphology ( J:122594 )

abnormal craniofacial development ( J:122594 )

• authors state that the phenotype observed is identical to that of Hectd1^opm homozygotes

vision/eye

abnormal eye morphology ( J:122594 )

• ocular dysplasia

abnormal eye distance/ position ( J:122594 )

microphthalmia ( J:122594 )

embryo

abnormal embryonic tissue morphology ( J:122594 )

• Authors state that the phenotype observed is identical to that of Hectd1^opm homozygotes

abnormal neural fold elevation formation ( J:122594 )

nervous system

exencephaly ( J:122594 )

• Authors state that the phenotype observed is identical to that of Hectd1^opm homozygotes

skeleton

abnormal neurocranium morphology ( J:122594 )

• authors state that the phenotype observed is identical to that of Hectd1^opm homozygotes

absent temporal bone petrous part ( J:122594 )

abnormal frontal bone morphology ( J:122594 )

absent interparietal bone ( J:122594 )

absent exoccipital bone ( J:122594 )

abnormal parietal bone morphology ( J:122594 )