Symbol Name ID |
Fancl
Fanconi anemia, complementation group L MGI:1914280 |
Darker colors indicate more annotations |
Human Phenotypes | Chromosome breakage |
Chromosomal breakage induced by crosslinking agents |
Disease(s) Associated with FANCL | ||
Fanconi anemia complementation group L |
Mouse Phenotypes | oligozoospermia |
decreased male germ cell number |
decreased primordial germ cell number |
absent germ cells |
decreased primordial germ cell proliferation |
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Availability | Mouse Genotype | |||||
Fanclgcd/Fanclgcd | ||||||
Fancltm1Ceb/Fancltm1Ceb | ||||||
Fanclgcd/Fancltm1Ceb |
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 |
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