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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID 		Alkbh1
alkB homolog 1, histone H2A dioxygenase
MGI:2384034
61 phenotypes from 4 alleles in 4 genetic backgrounds
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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 defecation J:211773
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
abnormal vibrissa morphology J:211773
enlarged lymph nodes 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
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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Send questions and comments to User Support. 		last database update
11/12/2024
MGI 6.24 		The Jackson Laboratory