Table 1.
Nucleotide position on chr 1 (mm9) | Genotype of Tsk2/+ | Genotype of B6 | Genotype of 101/H | Present in Other Strains? | Potential candidate for Tsk2? | Protein or mRNA containing substitution |
---|---|---|---|---|---|---|
SNP found by RNA-Seq | ||||||
44,675,490 | A | T | T | No | No, outside interval | Gulp1 Intron |
44,833,682* | C | T | T | No | YES | Gulp1Intron |
45,378,353* | A | T | T | No | YES | COL3A1 Exon (C33S) |
45,432,389 | C | G | Nd | Yes | No | Col5a2 3′UTR |
45,441,243 | C | A | C | No | No, in 101/H | Col5a2 Intron |
45,860,529 | G | A | G | Yes | No | Wdr75 Intron |
45,874,790 | T | C | T | Yes | No | Wdr75 Intron |
45,875,728 | C | T | C | Yes | No | Wdr75 Exon |
45,880,257 | CG | AC | CG | No | No, in 101/H | WDR75 Exon |
46,872,610 | T | G | Nd | Yes | No | Slc39a10 Intron |
46,874,711 | C | T | C | Yes | No | Slc39a10 Intron |
46,939,340 | T | C | T | Yes | No | BC040767 Intron |
46,939,624 | A | G | Nd | Yes | No | BC040767 Intron |
SNP found by 454 Sequencing | ||||||
44,833,682* | C | T | T | No | YES | Gulp1Intron |
45,378,353* | A | T | T | No | YES | COL3A1 Exon (C33S) |
45,465,923 | A | T | T | No | YES | Col5a2 Intron |
46,124,856 | A | G | A | Yes | No | Dnahc76 Intron |
46,124,857 | A | C | T | Yes | No | Dnahc76 Intron |
46,268,651 | C | T | T | No | No, outside interval | Dnahc76 Intron |
All single-copy nucleotide changes found by RNA-Seq or 454 sequencing were checked for their presence in other non-fibrotic strains (http://phenome.jax.org/) or individually verified by a phototyping assay (Bunce et al., 1995) and/or resequencing to confirm the single nucleotide change. SNP that were ruled out by one of these assays are considered not to be potential candidates for Tsk2. When known, genotypes shown for 101/H are from RNA-Seq, 454 sequencing or phototyping. Nd = not determined.
seen in both assays.