An 11-kb human genomic DNA fragment that includes the promoter and first intron of the chloride channel Kb (CLCNKB) gene, extending from the 3' end of the CLCNKA gene to immediately upstream of the translation start site of CLCNKB, is joined to the 5' end of a cDNA encoding a C-terminal hemagglutinin (HA) tagged, mutant human WNK lysine deficient protein kinase 4 with alanine replacing aspartic acid at amino acid position 564 (D564A), which resides in a highly conserved segment distal to the first coil domain of the protein, and followed by an SV40 polyadenylation signal. Immunoblot analysis of kidney homogenate using anti-HA antibody demonstrated expression in the kidney. Immunohistochemical analysis localized kidney expression of the mutant protein to the distal nephrons of the cortex and outer medulla, the thick ascending limb of Henley's loop (TAL) and, variably, cells of the distal tubules. In the last, signal is localized to the cytoplasm, while in TAL it is concentrated at the apical membrane. (J:110994)

Basic Information

Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
C57BL/6
--
Insertion
--
1
--
1

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

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PMID
Journal
Year
IF
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