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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fanci
Fanconi anemia, complementation group I
MGI:2384790
35 phenotypes from 4 alleles in 3 genetic backgrounds
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Allelic Composition
Genetic Background
Annotated Term Reference
Fanciem1Szh/Fanciem1Szh
Not Specified
no abnormal phenotype detected J:312543
Fanciem2Szh/Fanciem2Szh
Not Specified
abnormal DNA methylation during gametogenesis J:312543
decreased male germ cell number J:312543
decreased testis weight J:312543
female infertility J:312543
increased male germ cell apoptosis J:312543
male infertility J:312543
oligozoospermia J:312543
seminiferous tubule degeneration J:312543
small testis J:312543
Fancitm1.1Itl/Fancitm1.1Itl
involves: C57BL/6J * CBA
abnormal craniofacial morphology J:285384
abnormal fibroblast physiology J:285384
abnormal hematopoietic precursor cell morphology J:285384
abnormal hematopoietic stem cell physiology J:285384
abnormal lens development J:285384
abnormal pollex morphology J:285384
abnormal retina development J:285384
absent gametes J:285384
azoospermia J:285384
decreased birth body size J:285384
decreased body size J:285384
decreased body weight J:285384
decreased granulocyte monocyte progenitor cell number J:285384
decreased hematopoietic stem cell number J:285384
early cellular replicative senescence J:285384
embryonic lethality, incomplete penetrance J:285384
female infertility J:285384
fused phalanges J:285384
increased cellular sensitivity to DNA damaging agents J:285384
induced chromosome breakage J:285384
male infertility J:285384
malocclusion J:285384
microphthalmia J:285384
small gonad J:285384
spontaneous chromosome breakage J:285384
thrombocytopenia J:285384
Fancitm1a(EUCOMM)Wtsi/Fancitm1a(EUCOMM)Wtsi
C57BL/6N-Fancitm1a(EUCOMM)Wtsi/Wtsi
preweaning lethality, incomplete penetrance J:211773

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last database update
04/16/2024
MGI 6.23
The Jackson Laboratory