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Fig. 4 | BMC Genetics

Fig. 4

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

Fig. 4

Schematic representation of the genomic region of mouse chromosome 10 at 38.74–44.34 cM and the homologous regions in human. The genomic regions of mouse chromosome 10 at 38.74–44.34 cM are syntenic to human 12q23.2 – q23.3, 19p13.3, 19p13.12, 21q22.3 and 22q13.3. White dots represent mouse genetic markers used in this study: rs259766385 and rs239646663 are the peak markers of Tpir2. Black dots represent human genetic markers: rs2374688 and rs2839235 are the single nucleotide polymorphisms associated with urinary albumin excretion and glomerular filtration rate in human, respectively [21]; and PAH and D19S591 (also known as GATA44F10) are the genetic markers associated with urinary albumin excretion in patients with essential hypertension [22]. Chr., chromosome

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