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Mammalian Phenotype Ontology Annotations
Query Results - Summary
Symbol
Name
ID
Fancc
Fanconi anemia, complementation group C
MGI:95480
17 phenotypes from multigenic genotypes
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Allelic Composition
Genetic Background
Annotated Term Reference
Fancctm1Mab/Fancctm1Mab
Sod1tm1Cep/Sod1tm1Cep
involves: 129S1/Sv * 129X1/SvJ
abnormal bone marrow cell morphology/development J:71134
abnormal bone marrow morphology J:71134
abnormal common lymphocyte progenitor cell morphology J:71134
abnormal hepatocyte physiology J:71134
abnormal lymphocyte morphology J:71134
decreased bone marrow cell number J:71134
decreased common myeloid progenitor cell number J:71134
decreased erythrocyte cell number J:71134
decreased hemoglobin content J:71134
decreased leukocyte cell number J:71134
decreased lymphocyte cell number J:71134
decreased neutrophil cell number J:71134
increased mean corpuscular volume J:71134
microvesicular hepatic steatosis J:71134
pale liver J:71134
polychromatophilia J:71134
Fancctm1Mab/Fancctm1Mab
Terttm1Leah/Terttm1Leah
involves: 129P2/OlaHsd * 129S1/Sv * 129X1/SvJ * C57BL/6
abnormal cell physiology J:157096

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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last database update
04/23/2024
MGI 6.23
The Jackson Laboratory