70 phenotypes from 10 alleles in 9 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Mafem1(IMPC)Mbp/Maf+ C57BL/6N-Mafem1(IMPC)Mbp/MbpMmucd	abnormal heart morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal liver size	J:211773
	abnormal ovary morphology	J:211773
	abnormal spleen morphology	J:211773
	decreased prepulse inhibition	J:211773
	enlarged heart	J:211773
	enlarged kidney	J:211773
	enlarged ovary	J:211773
	enlarged spleen	J:211773
	increased circulating bilirubin level	J:211773
	increased freezing behavior	J:211773
	microphthalmia	J:211773
	small kidney	J:211773
	small liver	J:211773
	small spleen	J:211773
	urinary bladder obstruction	J:211773
Mafem1(IMPC)Mbp/Mafem1(IMPC)Mbp C57BL/6N-Mafem1(IMPC)Mbp/MbpMmucd	abnormal blood vessel morphology	J:211773
	abnormal liver size	J:211773
	abnormal placenta morphology	J:211773
	abnormal placenta vasculature	J:211773
	edema	J:211773
	embryonic growth retardation	J:211773
	microphthalmia	J:211773
	preweaning lethality, complete penetrance	J:211773
MafENU424/Maf+ involves: 102/El * C3H/El * C57BL/6El	nuclear cataract	J:121758
MafENU424/MafENU424 involves: 102/El * C3H/El * C57BL/6El	nuclear cataract	J:121758
MafOfl/Maf+ either: 102/ElH or C3H/HeH	abnormal pupillary reflex	J:82475
	cataract	J:82475
MafOfl/MafOfl either: 102/ElH or C3H/HeH	abnormal kidney morphology	J:82475
	abnormal lens induction	J:82475
	decreased body size	J:82475
	dilated renal tubule	J:82475
	increased urine glucose level	J:82475
	microphthalmia	J:82475
	neonatal lethality, incomplete penetrance	J:82475
	postnatal lethality, complete penetrance	J:82475
	small pupil	J:82475
	tremors	J:82475
	tubular nephritis	J:82475
Maftm1.1Cbm/Maftm2.1Cbm Isl1tm1(cre)Tmj/Isl1+ involves: 129P2/OlaHsd * 129X1/SvJ * C57BL/6 * SJL	abnormal axon morphology	J:181639
	abnormal coat/ hair morphology	J:181639
	abnormal Meissner's corpuscle morphology	J:181639
	abnormal nervous system electrophysiology	J:181639
	abnormal pacinian corpuscle morphology	J:181639
	axon degeneration	J:181639
	decreased body weight	J:181639
	decreased nerve conduction velocity	J:181639
	decreased pacinian corpuscle number	J:181639
	impaired coordination	J:181639
	small pacinian corpuscles	J:181639
Maftm1Glm/Maftm1Glm involves: 129/Sv * BALB/c	abnormal lens development	J:54079
	abnormal lens morphology	J:54079
	decreased body size	J:54079
	decreased interleukin-4 secretion	J:78382
	lethality throughout fetal growth and development, incomplete penetrance	J:54079
	microphthalmia	J:54079
	perinatal lethality, incomplete penetrance	J:54079
	postnatal lethality, incomplete penetrance	J:54079
	normal vision/eye phenotype	J:54079
Maftm1Gsb/Maftm1Gsb involves: 129S1/Sv * 129X1/SvJ * C57BL/6J	abnormal corneal endothelium morphology	J:56583
	abnormal eating behavior	J:56583
	abnormal lens development	J:56583
	abnormal lens vesicle development	J:56583
	increased cornea thickness	J:56583
	neonatal lethality, complete penetrance	J:56583
	shortened head	J:56583
	small lens	J:56583
	weakness	J:56583
Maftm1Mym/Maftm1Mym either: (involves: 129/Sv * C57BL/6J) or (involves: 129/Sv * ICR)	abnormal lens development	J:56095
	abnormal lens fiber morphology	J:56095
	embryonic lethality during organogenesis, incomplete penetrance	J:56095
	postnatal lethality, complete penetrance	J:56095
Tg(Igh-Maf)68Staka/0 C57BL/6-Tg(Igh-Maf)68Staka	abnormal spleen morphology	J:168074
	enlarged spleen	J:168074
	increased IgG level	J:168074
	increased IgM level	J:168074
	increased immunoglobulin level	J:168074
	increased lymphoma incidence	J:168074
	increased plasma cell number	J:168074
	renal cast	J:168074
Tg(Igh-Maf)524Staka/0 involves: C57BL/6 * C57BL/6J * DBA/2	abnormal spleen morphology	J:168074
	enlarged spleen	J:168074
	increased IgG level	J:168074
	increased IgM level	J:168074
	increased immunoglobulin level	J:168074
	increased lymphoma incidence	J:168074
	increased plasma cell number	J:168074
	renal cast	J:168074