60 phenotypes from 4 alleles in 4 genetic backgrounds

Allelic Composition Genetic Background	Annotated Term	Reference
Alkbh1tm1.1Lpkn/Alkbh1tm1.1Lpkn involves: 129S/SvEv * FVB/N	abnormal placenta junctional zone morphology	J:131022
	decreased birth weight	J:131022
	decreased fetal size	J:131022
	decreased placenta weight	J:131022
	decreased placental labyrinth size	J:131022
	decreased spongiotrophoblast cell number	J:131022
	decreased trophoblast giant cell number	J:131022
	decreased trophoblast glycogen cell number	J:131022
	fetal growth retardation	J:131022
	pale placenta	J:131022
Alkbh1tm1b(EUCOMM)Hmgu/Alkbh1+ C57BL/6N-Alkbh1tm1b(EUCOMM)Hmgu/Ieg	abnormal ileum morphology	J:211773
	abnormal kidney morphology	J:211773
	abnormal liver morphology	J:211773
	abnormal mammary gland morphology	J:211773
	abnormal spleen morphology	J:211773
	enlarged lymph nodes	J:211773
	increased plasmacytoid dendritic cell number	J:211773
Alkbh1tm1b(EUCOMM)Hmgu/Alkbh1tm1b(EUCOMM)Hmgu C57BL/6N-Alkbh1tm1b(EUCOMM)Hmgu/Ieg	preweaning lethality, complete penetrance	J:211773
Alkbh1tm1Klng/Alkbh1+ involves: 129X1/SvJ * C57BL/6	abnormal neural tube closure	J:166841
	abnormal survival	J:166841
	anophthalmia	J:166841
	broad snout	J:166841
	decreased litter size	J:166841
	decreased survivor rate	J:166841
	exencephaly	J:166841
	microphthalmia	J:166841
	short snout	J:166841
Alkbh1tm1Klng/Alkbh1tm1Klng involves: 129X1/SvJ * C57BL/6	abnormal cell physiology	J:200274
	abnormal eye morphology	J:166841
	abnormal frontal bone morphology	J:166841
	abnormal interparietal bone morphology	J:166841
	abnormal lens fiber morphology	J:166841
	abnormal lens morphology	J:166841
	abnormal mandible morphology	J:166841
	abnormal metatarsal bone morphology	J:166841
	abnormal neural tube closure	J:166841
	abnormal parietal bone morphology	J:166841
	abnormal phalanx morphology	J:166841
	abnormal seminiferous tubule morphology	J:166841
	abnormal sternum morphology	J:166841
	abnormal sternum ossification	J:166841
	abnormal survival	J:166841
	abnormal tooth development	J:166841
	absent nasal bone	J:166841
	acoria	J:166841
	anophthalmia	J:166841
	aphakia	J:166841
	decreased bone ossification	J:166841
	decreased fetal size	J:166841
	decreased litter size	J:166841
	decreased male germ cell number	J:166841
	decreased survivor rate	J:166841
	decreased testis weight	J:166841
	delayed cranial suture closure	J:166841
	delayed intramembranous bone ossification	J:166841
	disorganized retina layers	J:166841
	exencephaly	J:166841
	intracranial hemorrhage	J:166841
	lens dislocation	J:166841
	microphthalmia	J:166841
	postnatal growth retardation	J:166841
	retina degeneration	J:166841
	seminiferous tubule degeneration	J:166841
	short frontal bone	J:166841
	short nasal bone	J:166841
	short snout	J:166841
	small testis	J:166841
	wide cranial sutures	J:166841
Alkbh1tm1Lpkn/Alkbh1tm1Lpkn involves: 129S/SvEv	normal reproductive system phenotype	J:131022