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Ifi44lH28-c
Spontaneous Allele Detail
Nomenclature
Symbol: Ifi44lH28-c
Name: interferon-induced protein 44 like; histocompatibility 28, c variant
MGI ID: MGI:6199480
Synonyms: H28c
Gene: Ifi44l  Location: Chr3:151464374-151468528 bp, - strand  Genetic Position: Chr3, 76.94 cM
Mutation
origin
Strain of Origin:  BALB/cBy
Mutation
description
Allele Type:    Spontaneous (Not Applicable)
Mutation:    Not Specified
 
Mutation detailsThis minor histocompatibility antigen, formerly designated H28, was traced to the ILENFPRL peptide from this gene in the BALB/cBy genome, distinct from the sequence in the C57BL/6J genome. This peptide is presented in Kb and stimulates C57BL/6By hosts to reject BALB.B grafts. (J:64705)
Inheritance:    Codominant
Find Mice (IMSR)
Mouse strains and cell lines available from the International Mouse Strain Resource (IMSR)
Carrying this Mutation:  Mouse Strains: 4 strains available      Cell Lines: 0 lines available
Carrying any Ifi44l Mutation:  13 strains or lines available
References
Original:  J:4420 Bailey DW, Genetics of histocompatibility in mice. I. New loci and congenic lines. Immunogenetics. 1975;2:249-256
All:  3 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
11/30/2021
MGI 6.17
The Jackson Laboratory