Symbol Name ID |
Cfp
complement factor properdin MGI:97545 |
Darker colors indicate more annotations |
Human Phenotypes | Dysfunctional alternative complement pathway |
Disease(s) Associated with CFP | |
X-linked properdin deficiency |
Mouse Phenotypes | abnormal complement pathway |
impaired complement alternative pathway |
impaired complement classical pathway |
decreased susceptibility to induced arthritis |
sepsis |
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Availability | Mouse Genotype | |||||
Cfptm1Cmst/Cfptm1Cmst | ||||||
Cfptm1Song/Cfptm1Song | ||||||
Cfptm1Song/Y | ||||||
Cfptm2.1Song/Cfptm2.1Song Tg(EIIa-cre)C5379Lmgd/0 (conditional) |
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Cfptm2.1Song/Cfptm2.1Song Lyz2tm1(cre)Ifo/Lyz2+ (conditional) |
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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