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. 2007 Aug 1;8(8):R154. doi: 10.1186/gb-2007-8-8-r154

Table 1.

Unusual TG splice acceptors identified in the human transcriptome

Intron 3' Splice site pair ESTs for unusual 3' splice sites



Gene No. Length Distance Motif Fraction No.
GNAS 3 7843 3 CTG,CAG| 0.15-0.62* 282
PCGF2 1 224 3 AAG|ATG, 0.50 4
CNBP 3 168 3 TTGTTG,AAG| 0.25 257
3 168 6 TTG,TTGAAG| 0.01 10
FBXO17 3 1999 3 CAG|ATG, 0.14 4
C21orf63 3 9975 3 CAG|ATG, 0.09 2
BRUNOL4 6 1147 3 CAG|CTG, 0.07 2
PCID2 2 2162 3 CAG|ATG, 0.04 7
TNNT2 1 4354 3 TTG,GAG| 0.04 2
CACNA1A 9 2532 3 TTGTTG,GAG| ? -
9 2532 6 TTG,TTGGAG| 0.17 -
GPBP1 9 1377 4 CAG|GATG, 0.03 2
KIAA0494 1 1459 5 TTG,AGCAG| 0.09 2
OSBPL8 2 36530 6 CTG,TTGTAG| 0.11 2
SAP30 1 1892 6 CTG,TTTCAG| 0.04 2
DRD2 6 1485 6 CTG,GTGCAG| 0.02 5
SUV420H2 5 134 7 CTG,GCTCCAG| 0.20 3
SSRP1 1 489 7 TTG,AATTCAG| 0.20 16
FREQ 2 16849 7 CTG,CCTCCAG| 0.04 2
IL21 3 2753 8 TTG,ATTTCTAG| 0.13 2
RYK 7 3107 9 TTG,GCTCCTTAG| 0.77 27
DLG4 5 131 9 CTG,GAGTTGCAG| 0.62 8
SMARCA4 29 6174 9 TTG,ACCCTGAAG| 0.41 34
FBXL10 15 177 9 TTG,GCCTACAAG| 0.21 3
HNRPR 7 2839 9 TTG,GTTTAACAG| 0.13 15
RRAD 1 214 9 CTG,ATCCCCTAG| 0.06 2
TGM1 6 454 10 CTG,TCCTGGGCAG| 0.13 2
ALAS1 11 1599 11 CTG,TTTCTCCTCAG| 0.04 5
ARS2 18 182 12 TTG,TACTCCCCCCAG| 0.74 75
PCBP2 7 1337 12 CTG,ACTCTCTCCCAG| 0.43 169
PTPN11 10 4269 12 TTG,GCTCTACTCCAG| 0.33 3
MSH5 6 164 12 CTG,ATCCCCTCCCAG| 0.25 5
SYTL2 9 1259 13 TTG,CCCTCCTGAGTAG| 0.09 3
TOMM40 1 95 16 CTG,ACCTCTCCCCTAGCAG| 0.07 2
MARK3 3 20478 17 TTG,TTTGTTTTTTTTTTTAG| 0.07 3
BAT3 6 832 18 CTG,ACTCTCCCCTACCTTCAG| 0.01 1
SH3D19 6 838 21 TTG,GTTTTGTTTTGGTCTCGTCAG| 0.07 1
LOC346653 1 3097 27 CTG,ACCCATGTACCTGAGGCTGATTTCCAG| 0.60 3
ACAD9 10 253 28 TTG,TTTCTTGTGTTTTTTCTGAACACTCCAG| 0.09 4

Entries in bold have RefSeq transcripts supporting the unusual TG acceptor site. Each TG splice variant is supported by at least two ESTs and at least 3% of all covering ESTs, except for some RefSeq-supported cases, CACNA1A [24,35], DRD2 [19] and BAT3. In the 'Motif' column, a vertical line (|) indicates a canonical splice site, and a comma (,) marks the TG splice site. Splice ratios are given as absolute EST counts (No.) as well as the fraction of TG splice variants. A question mark indicates that an explicit fraction is not given in the referenced article, although the authors performed quantitative experiments. *EST ratio depends on the exon junction; the upstream exon 3 may be skipped. Splice variants were previously quantified by others: GNAS [16,26], CACNA1A (splice ratio cited from [24,35]), DRD2 (splice ratio cited from [19]). Alternative splicing at FBXO17 intron 3 was not experimentally reproducible in this study.