Special

GgaINT0139185 @ galGal4

Intron Retention

Gene
Description
suppression of tumorigenicity 14 (colon carcinoma) [Source:HGNC Symbol;Acc:HGNC:11344]
Coordinates
chr24:1577729-1578163:+
Coord C1 exon
chr24:1577729-1577842
Coord A exon
chr24:1577843-1578034
Coord C2 exon
chr24:1578035-1578163
Length
192 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
CTCCCTTTGGCCTTCCACAGCAG
3' ss Score
8.02
Exon sequences
Seq C1 exon
GTTGTGCAAACAACAGCTTCAAGTGCAACAATGGGAAGTGCATCCCCAACACACAGAAGTGTGATGGCAAGGACGACTGCGGGGATGGGAGCGATGAGGGCACCTGCAGCAAAG
Seq A exon
GTGAGGATGGGCTGTGGTGGGGACCTCCCTTGAAATGCAGCTTCTTATGGATGTACTCATGGCTGGGCAGCCTGGAGTGCATTTCTGCCCGCAGTGGCAATGTCCTGGGGTGGGCAGAAGTGGGGAGGGGCTTCTGAGCAGCACAGTTTCCCCAGCACTGGGACTAACCCTTCTCCCTTTGGCCTTCCACAG
Seq C2 exon
CAGCCCAGTCAACAGTTGCCTGCAAGAGCTACACGTACAAATGCCGCAATGGGCTCTGCATCAGCAAGCAGAACCCGGAGTGTGATGGGCAGAAGGACTGCGAAGACAATTCTGATGAGGACAATTGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001331:ENSGALT00000002027:13
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:
PF0005713=Ldl_recept_a=WD(100=92.3)
A:
NA
C2:
PF0005713=Ldl_recept_a=WD(100=86.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTTGTGCAAACAACAGCTTCA
R:
TGCAATTGTCCTCATCAGAATTGT
Band lengths:
243-435
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]