MGI MP annotations for MGI:102524: Pou4f2

Gray arrows indicate "is_a"



Compare annotations to MP categories for MGI:102524.

• Entry indicates phenotypic allele for this gene.
• Colored entries indicate MP annotation.

ID	Term	Pou4f2tm1.1Xmu	Pou4f2tm1Nat	Pou4f2tm1Rsd	Pou4f2tm3Whk
MP:0005386	behavior/neurological phenotype	Pou4f2tm1.1Xmu	Pou4f2tm1Nat	Pou4f2tm1Rsd	Pou4f2tm3Whk
MP:0003631	nervous system phenotype	Pou4f2tm1.1Xmu	Pou4f2tm1Nat	Pou4f2tm1Rsd	Pou4f2tm3Whk
MP:0002873	normal phenotype	Pou4f2tm1.1Xmu	Pou4f2tm1Nat	Pou4f2tm1Rsd	Pou4f2tm3Whk
MP:0005391	vision/eye phenotype	Pou4f2tm1.1Xmu	Pou4f2tm1Nat	Pou4f2tm1Rsd	Pou4f2tm3Whk

Full set of annotations for MGI:102524

ID	Term	Allele	Alleles	Background	Color Key
MP:0002561	abnormal circadian phase	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0005551	abnormal eye electrophysiology	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	B6.129S7-Pou4f2	color key
MP:0004811	abnormal neuron physiology	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0001330	abnormal optic nerve morphology	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0001325	abnormal retina morphology	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0008056	abnormal retinal ganglion cell morphology	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0006303	abnormal retinal nerve fiber layer morphology	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0000967	abnormal sensory neuron projections	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0000904	abnormal superior colliculus morphology	Pou4f2tm1Rsd	Pou4f2tm1Rsd/Pou4f2tm1Rsd	involves: 129S4/SvJae	color key
MP:0006156	abnormal visual pursuit	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0006309	decreased retinal ganglion cell number	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	B6.129S7-Pou4f2	color key
MP:0006309	decreased retinal ganglion cell number	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0006309	decreased retinal ganglion cell number	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0008105	increased amacrine cell number	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0002003	miotic pupils	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0002169	no abnormal phenotype detected	Pou4f2tm1.1Xmu	Pou4f2tm1.1Xmu/Pou4f2tm1.1Xmu	involves: 129S6/SvEvTac * C57BL/6	color key
MP:0006221	optic nerve hypoplasia	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0002984	retina hypoplasia	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0008067	retinal ganglion cell degeneration	Pou4f2tm1Rsd	Pou4f2tm1Rsd/Pou4f2tm1Rsd	involves: 129S4/SvJae	color key
MP:0002563	shortened circadian period	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0008507	thin retinal ganglion layer	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0008507	thin retinal ganglion layer	Pou4f2tm3Whk	Pou4f2tm3Whk/Pou4f2tm3Whk	Not Specified	color key
MP:0008511	thin retinal inner nuclear layer	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key
MP:0008515	thin retinal outer nuclear layer	Pou4f2tm1Nat	Pou4f2tm1Nat/Pou4f2tm1Nat	involves: 129S7/SvEvBrd * C57BL/6	color key