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The Bph13 gene was located near the bph19 gene on chromosome 3S.
Expression of a reporter gene in transgenic Arabidopsis under control of promoter of each gene was located in the phloem.
The second BSA revealed that markers and the sug-h phenotype co-segregated on chromosome 4, indicating that the second gene was located on chromosome 4.
The BPH31 gene was located on the long arm of chromosome 3 within an interval of 475 kb between the markers PA26 and RM2334.
The la gene was located between R728 and C459B, of which the positions were 63.8 and 65.2, respectively, in the map by Harushima et al. (1998).
The TaCYP707A1 gene was located on chromosome 6BL using a set of Chinese Spring nullisomic-tetrasomic lines and ditelosomic line 6BS.
Phylogenetic analysis indicated that the AmphiTAB1 gene was located between invertebrates and vertebrates, suggesting that the AmphiTAB1 gene is a member of the TAB1 gene family.
In Kasumi-3, this gene was located in a larger deleted region of 4.37 Mb on 7p22.
Ultimately, we determined approximately 13.8-kb genomic sequence and revealed that the OnubOR3 gene was located in a 1.85-kb interval upstream of the OnubOR1 genes (Fig. 2).
Meanwhile, SNP rs11571316 in the promoter of the CTLA4 gene was located on one of the two LD blocks that did not include SNP rs231779 (Fig. 1G).
III) The gene was located in a heterozygously deleted region.
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