Phenotypes Associated with This Genotype

Genotype
MGI:5472140

• Allelic Composition: Neurod1^{tm1.1(Atoh7)Whk}/Neurod1^{tm1.1(Atoh7)Whk}
• Genetic Background: Not Specified

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

behavior/neurological

head tilt ( J:194077 )

circling ( J:194077 )

nervous system

abnormal cerebellum morphology ( J:194077 )

• similar to mice homozygous for Neurod1^tm1Mjts

abnormal retina ganglion cell morphology ( J:194077 )

• displaced cells are found in the inner most region of the inner nuclear layer

increased retina ganglion cell number ( J:194077 )

• displaced cells are found in the inner most region of the inner nuclear layer

abnormal retina cone cell morphology ( J:194077 )

• all cone photoreceptors in the dorsal retina express the short-wavelength (S) opsin indicating a loss of M cone cells

vision/eye

abnormal retina cone cell morphology ( J:194077 )

• all cone photoreceptors in the dorsal retina express the short-wavelength (S) opsin indicating a loss of M cone cells

abnormal retina ganglion layer morphology ( J:194077 )

• increase in the density of retinal ganglion cell axon bundles in the retina at P30

abnormal retina ganglion cell morphology ( J:194077 )

• displaced cells are found in the inner most region of the inner nuclear layer

increased retina ganglion cell number ( J:194077 )

• displaced cells are found in the inner most region of the inner nuclear layer

abnormal retina inner nuclear layer morphology ( J:194077 )

• displaced retinal ganglion cells are found in the inner most region of the inner nuclear layer