The mutant phenotype was discovered in a screen of macrophages from G3 progeny of an ENU mutagenized male mouse for their ability to control viral infection. The mutation has been identified as an A to C transversion at nucleotide position 1150 (Genbank: NM_010508), in the eighth of the gene's 11 exons. It results in replacement of threonine by proline at amino acid position 341 of the protein (T341P), in its extracellular domain. (J:142790)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
C57BL/6J
Chemically induced
Single point
Recessive
1
1
2

Phenotypes

Legend:
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes:
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Phenotypes

References Literature

Title
PMID
Journal
Year
IF
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