GgaINT0139188 @ galGal4
Intron Retention
Gene
ENSGALG00000001331 | ST14
Description
suppression of tumorigenicity 14 (colon carcinoma) [Source:HGNC Symbol;Acc:HGNC:11344]
Coordinates
chr24:1579111-1579754:+
Coord C1 exon
chr24:1579111-1579385
Coord A exon
chr24:1579386-1579617
Coord C2 exon
chr24:1579618-1579754
Length
232 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGC
5' ss Score
9.85
3' ss Seq
GCTGTTTCTGGTCCTTGCAGGCA
3' ss Score
9.47
Exon sequences
Seq C1 exon
CTACTCAGACGCCAGCCTGTGGACAGCCTACCTGGGCCTGACCAACCAAAGCAAACGCAACGATGCCAACGTGCAAATGAAGCAAATCAAGCGCATCATCTCCCACCGTTCCTTCAATGACTACACCTACGACTATGATATTGCTGTGATAGAGCTGCAGAGCCCCGTCACCTTCTCCGCTGTCGTCCAGCCCATCTGCCTGCCCGATTCTACGCACAACTTCCCCGTGGGCAAAGACCTGTGGGTGACCGGATGGGGAGCGACCGTGGAAGGAG
Seq A exon
GTAAGCACTGAAGTGATTTAGCTTGCTGGGAAACCAGAATCAGATGTAATTCGCTTGGGAGCGCACACGGTTGAGGTCCCAGAGCTCAAGGGAAAACTGCAGTAGTTGCAGTGGGGATAATTAATTGGTCATTTGTTAGGAGCCTGAATGAAGCATACAGGTATGAGACTGTGCAGGGGAGAGGACTGCTGCTAAACGGACTTTGTGCTTACGCTGTTTCTGGTCCTTGCAG
Seq C2 exon
GCAGCGGATCCACCATCTTGCAGAAAGCAGAAATCCGGGTGATCAACCAAACCGTCTGCAACCGGCTGCTGACCGACCAGCTGACAGAGCGCATGATGTGCGTGGGGGTCCTGACGGGCGGCGTGGATGCGTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001331:ENSGALT00000002027:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0008921=Trypsin=FE(39.1=100)
A:
NA
C2:
PF0008921=Trypsin=FE(19.1=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACCAACCAAAGCAAACGCAAC
R:
AGACGGTTTGGTTGATCACCC
Band lengths:
292-524
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]