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Table 5 Hematological analysis of line Kctd1 I27N

From: Standardized, systemic phenotypic analysis reveals kidney dysfunction as main alteration of Kctd1 I27N mutant mice

Parameter

Heterozygous mutant males

Wild-type males

Heterozygous mutant females

Wild-type males

Genotype:

P-value

WBC (103/μl)

10.6 ± 1.5

10.6 ± 2.0

10.9 ± 1.8

9.6 ± 1.2

 

RBC (106/μl)

9.5 ± 0.4

10.2 ± 0.3

9.8 ± 0.4

9.8 ± 0.3

0.001

PLT (103/μl)

989 ± 158

1051 ± 72

982 ± 63

1002 ± 60

 

HGB (g/dl)

15.4 ± 0.6

16.5 ± 0.5

15.7 ± 0.6

16.3 ± 0.8

< 0.001

HCT (%)

44.8 ± 1.7

48.1 ± 1.3

46.0 ± 1.7

46.6 ± 1.3

< 0.001

MCV (fl)

47.1 ± 0.6

47.3 ± 0.5

47.1 ± 0.5

47.6 ± 0.6

0.005

MCH (pg)

16.1 ± 0.5

16.2 ± 0.3

16.1 ± 0.3

16.6 ± 0.5

0.005

MCHC (g/dl)

34.3 ± 1.0

34.2 ± 0.5

34.3 ± 0.7

34.9 ± 1.0

 
  1. 17-week-old mice were tested. Number per genotype and sex: n = 14–15. Data are presented as mean ± standard deviation. Significance vs. wild-type controls: Exact P values are indicated for P < 0.05
  2. WBC white blood cell count, RBC red blood cell count, PLT platelet count, HGB hemoglobin, HCT hematocrit, MCV mean corpuscular volume, MCH mean corpuscular hemoglobin, MCHC mean corpuscular hemoglobin concentration