Nineteen strains (129X1/Sv, 129P2/OlaHsd, 129S1/SvImJ, 129S5SvEvBrd, AKR/J, A/J, BALB/cJ, C3H/HeH, C3H/HeJ, CBA/J, DBA/1J, DBA/2J, LP/J, NZO/HILtJ, RF/J, SEA/GnJ, FVB/NCrl, FVB/NJ, BUB/BnJ, ZALENDE/EiJ, LEWES/EiJ and WSB/EiJ) contain an in-frame 12 bp deletion within the gene spanning the basepairs 424 to 435. Immunocytochemistry analysis confirmed the absence of protein expression in vomeronasal sensory epithelium and neutrophil granulocytes. Furthermore, HEK293T cells expressing Fpr3del showed missing receptor protein expression and loss of function. This deletion is not detected in 13 other strains (C57Bl/6NCrl, C57Bl/6NJ, C57Bl/10J, C57BR/cdJ, C57L/J, C58/J, I/LnJ, NZB/B1NJ, NZB/Ola, NZW/LacJ, KK/HiJa, NOD/ShiLtJ, ST/bJ, SPRET/EiJ, CZE/DT, PWK/PhJ, GER/DT, FRA/DT, CAST/EiJ and KAZ/DT). (J:233707)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Related Gene
Related Disease
Reference
various
Spontaneous
Intragenic deletion
--
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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