64 phenotypes from 14 alleles in 19 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Agtpbp1atms/Agtpbp1atms MRL/Mp-Agtpbp1atms	abnormal lymphocyte cell number	J:103944
	abnormal spleen morphology	J:103944
	abnormal T cell differentiation	J:103944
	abnormal T cell physiology	J:103944
	abnormal T cell subpopulation ratio	J:103944
	ataxia	J:103944
	decreased B cell number	J:103944
	decreased spleen weight	J:103944
	increased CD4-positive, alpha-beta T cell number	J:103944
	increased CD8-positive, alpha-beta T cell number	J:103944
	spleen hypoplasia	J:103944
Agtpbp1atms/Agtpbp1atms MRL/Mp-Agtpbp1atms Faslpr	ataxia	J:103944
	decreased spleen weight	J:103944
Agtpbp1babe/Agtpbp1babe C57BL/6JSfdAnu-Agtpbp1babe/Anu	ataxia	J:104190
	paraparesis	J:104190
Agtpbp1m2Btlr/Agtpbp1m2Btlr C57BL/6J-Agtpbp1m2Btlr	decreased activated sperm motility	J:159361
	decreased body size	J:159361
	tremors	J:159361
Agtpbp1m3Btlr/Agtpbp1m3Btlr C57BL/6J-Agtpbp1m3Btlr	decreased body weight	J:265119
	impaired coordination	J:265119
Agtpbp1pcd-2J/Agtpbp1pcd-2J involves: SM/J	abnormal motor coordination/balance	J:74929
	ataxia	J:74929
	normal nervous system phenotype	J:74929
	reduced male fertility	J:74929
Agtpbp1pcd-3J/Agtpbp1pcd-3J BALB/cByJ-Agtpbp1pcd-3J/J	normal behavior/neurological phenotype	J:233744
	normal hematopoietic system phenotype	J:233744
	normal homeostasis/metabolism phenotype	J:233744
Agtpbp1pcd-3J/Agtpbp1pcd-3J involves: BALB/cByJ	abnormal cerebellar granule layer morphology	J:74929
	abnormal male germ cell morphology	J:74929
	abnormal mitral cell morphology	J:74929
	abnormal thalamus morphology	J:74929
	asthenozoospermia	J:74929
	ataxia	J:74929
	normal immune system phenotype	J:231311
	male infertility	J:74929
	oligozoospermia	J:74929
	Purkinje cell degeneration	J:74929
	retina photoreceptor degeneration	J:74929
Agtpbp1pcd-4J/Agtpbp1pcd-4J involves: C3H * C57BL/6J	ataxia	J:78314
	Purkinje cell degeneration	J:78314
Agtpbp1pcd-5J/Agtpbp1pcd-5J involves: DBA/2J	abnormal photoreceptor inner segment morphology	J:105316
	abnormal photoreceptor outer segment morphology	J:105316
	abnormal retina photoreceptor layer morphology	J:105316
	ataxia	J:83266, J:105316
	male infertility	J:105316
	Purkinje cell degeneration	J:83266, J:105316
	retina degeneration	J:105316
	small cerebellum	J:105316
	thin retina outer nuclear layer	J:105316
Agtpbp1pcd-6J/Agtpbp1+ C57BL/6J-Agtpbp1pcd-6J/J	reduced fertility	J:87349
Agtpbp1pcd-6J/Agtpbp1pcd-6J C57BL/6J-Agtpbp1pcd-6J/J	abnormal olfactory bulb morphology	J:87349
	abnormal ventral spinal root morphology	J:87349
	ataxia	J:87349
	azoospermia	J:87349
	decreased skeletal muscle fiber size	J:87349
	infertility	J:87349
	Purkinje cell degeneration	J:87349
	retina degeneration	J:87349
	testicular atrophy	J:87349
Agtpbp1pcd-7J/Agtpbp1pcd-7J C.Cg-Ighmtm1Cgn Agtpbp1pcd-7J	abnormal auditory brainstem response	J:96855
	ataxia	J:96855
	enlarged hippocampus	J:96855
	Purkinje cell degeneration	J:96855
Agtpbp1pcd-8J/Agtpbp1pcd-8J BALB/cJ-Agtpbp1pcd-8J/GrsrJ	abnormal male germ cell morphology	J:132487
	abnormal retina layer morphology	J:132487
	ataxia	J:132487
	decreased body size	J:132487
	decreased Purkinje cell number	J:132487
	male infertility	J:132487
	reduced female fertility	J:132487
	retina degeneration	J:132487
Agtpbp1pcd-Btlr/Agtpbp1pcd-Btlr C57BL/6J-Agtpbp1pcd-Btlr	ataxia	J:133627
	male infertility	J:133627
	normal nervous system phenotype	J:133627
	oligozoospermia	J:133627
	Purkinje cell degeneration	J:133627
	retina photoreceptor degeneration	J:133627
	teratozoospermia	J:133627
Agtpbp1pcd-Tg(Dhfr)1Jwg/Agtpbp1pcd-Tg(Dhfr)1Jwg involves: C57BL/6J * CD-1 * DBA/2J	abnormal olfactory bulb morphology	J:9814, J:14991
	ataxia	J:9814, J:14991
	azoospermia	J:9814
	decreased litter size	J:9814
	male infertility	J:9814, J:14991
	Purkinje cell degeneration	J:9814, J:14991
	retina photoreceptor degeneration	J:9814, J:14991
Agtpbp1pcd/Agtpbp1pcd B6.BR-Agtpbp1pcd/J	abnormal photoreceptor connecting cilium morphology	J:249732
	retina photoreceptor degeneration	J:249732
Agtpbp1pcd/Agtpbp1pcd involves: C57BL/6J * C57BR/cdJ * DBA/2J	abnormal cone electrophysiology	J:189268
	abnormal eye electrophysiology	J:189268
	abnormal retina inner plexiform layer morphology	J:189268
	abnormal retina outer nuclear layer morphology	J:189268
	abnormal retina rod cell morphology	J:189268
	abnormal rod electrophysiology	J:189268
	decreased amacrine cell number	J:189268
	retina photoreceptor degeneration	J:189268
	thin retina outer nuclear layer	J:189268
Agtpbp1pcd/Agtpbp1pcd involves: C57BR/cdJ	abnormal cochlear VIII nucleus morphology	J:121314
	decreased Purkinje cell number	J:121314
Agtpbp1pcd/Agtpbp1pcd involves: C57BR/cdJ * CBA	abnormal cerebellar granule layer morphology	J:5613
	abnormal cerebellar Purkinje cell layer	J:23733, J:106414
	abnormal male germ cell morphology	J:5613
	abnormal olfactory bulb morphology	J:5613
	abnormal Purkinje cell dendrite morphology	J:23733
	abnormal thalamus morphology	J:5613
	asthenozoospermia	J:5613
	ataxia	J:5613
	decreased Purkinje cell number	J:106414
	male infertility	J:5613
	oligozoospermia	J:5613
	Purkinje cell degeneration	J:5613
	reduced female fertility	J:5613
	retina photoreceptor degeneration	J:5613