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Fibcd1tm1Spte
Targeted Allele Detail
Summary
Symbol: Fibcd1tm1Spte
Name: fibrinogen C domain containing 1; targeted mutation 1, Steven P Templeton
MGI ID: MGI:7567874
Gene: Fibcd1  Location: Chr2:31703302-31736017 bp, - strand  Genetic Position: Chr2, 21.89 cM
Alliance: Fibcd1tm1Spte page
Mutation
origin
Germline Transmission:  Earliest citation of germline transmission: J:340107
Parent Cell Line:  CJ7 (ES Cell)
Strain of Origin:  129S1/Sv-Oca2+ Tyr+ Kitl+
Mutation
description
Allele Type:    Targeted (Null/knockout)
Mutation:    Intragenic deletion
    A neomycin resistance gene replaced exon 2. (J:340107)
Phenotypes
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View phenotypes and curated references for all genotypes (concatenated display).
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 0 strains available      Cell Lines: 0 lines available
Carrying any Fibcd1 Mutation:  22 strains or lines available
References
Original:  J:340107 Bhattacharya S, et al., FIBCD1 Deficiency Decreases Disease Severity in a Murine Model of Invasive Pulmonary Aspergillosis. Immunohorizons. 2021 Dec 22;5(12):983-993
All:  2 reference(s)

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
10/29/2024
MGI 6.24
The Jackson Laboratory