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Hcfc2sca
Chemically induced Allele Detail
Summary
Symbol: Hcfc2sca
Name: host cell factor C2; scaffold
MGI ID: MGI:6108106
Gene: Hcfc2  Location: Chr10:82531994-82578262 bp, + strand  Genetic Position: Chr10, 39.93 cM
Alliance: Hcfc2sca page
Mutation
origin
Strain of Origin:  C57BL/6J
Mutation
description
Allele Type:    Chemically induced (ENU) (Hypomorph)
Mutation:    Single point mutation
 
Mutation detailsENU mutagenesis induced a T to A point mutation that results in the amino acid substitution of isoleucine for phenylalanine at position 599 (F599I). (J:251008)
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: 1 strain available      Cell Lines: 0 lines available
Carrying any Hcfc2 Mutation:  32 strains or lines available
References
Original:  J:251008 Sun L, et al., HCFC2 is needed for IRF1- and IRF2-dependent Tlr3 transcription and for survival during viral infections. J Exp Med. 2017 Nov 06;214(11):3263-3277
All:  1 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
04/23/2024
MGI 6.23
The Jackson Laboratory