Genetic loci for resistance to podocyte injury caused by the tensin2 gene deficiency in mice

BMC Genomic Data

Table 2 Relationship between albuminuria and combined genotypes of chromosomes 2 and 10 (rs259766385)

Chromosome	Marker	Position (cM)	χ² (P)				Student-T (P)^c
Chromosome	Marker	Position (cM)	Min/Max^a	50%^b	40%^b	30%^b	Min/Max	50%	40%	30%
2	D2Mit398	61.76	0.003	0.0019	0.0049	0.014	0.055	0.078	0.075	0.027
2	rs214164633	65.66	0.0013	0.0012	0.0027	0.046	0.0016	0.0045	0.0028	0.0010
2	rs234188972	70.98	0.0013	0.00090	0.0032	0.0097	0.00021	0.0015	0.00083	0.00025
2	rs247793542	75.41	0.0063	0.0054	0.012	0.024	0.0020	0.0070	0.0042	0.0013
2	rs228447345	81.91	0.0039	0.0021	0.012	0.10	0.0089	0.028	0.025	0.015

^aThe N2 mice with urinary albumin excretion larger than 3.1 g/gCr, the minimum value in FVB-Tns2^nph mice, were defined as the FVB type (affected) and the N2 mice with urinary albumin excretion less than 0.7 g/gCr, the maximum value in B6- Tns2^nph mice, were defined as the B6 type (not affected)
^bThe upper X% and lower X% of N2 mice in urinary albumin excretion were defined as the FVB type (affected) and the B6 type (not affected), respectively
^cUrinary albumin excretion in the homogeneic genotype, in which both markers were FVB/FVB genotype, were compared with those in the heterogeneic genotype, in which at least one of the markers was B6/FVB genotype

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