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This histocompatibility haplotype was identified in inbred donors I/St, JK/St, and WB/Re and has a unique j specificity in H2-K through H2-Ebeta then H2-Db, H2-Lb, Qa2a, H2-T18b, and Qa1b. (J:23864)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
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 |
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References Literature
Title
PMID
Journal
Year
IF
