Special

GgaEX1055673 @ galGal4

Exon Skipping

Gene
Description
suppression of tumorigenicity 14 (colon carcinoma) [Source:HGNC Symbol;Acc:HGNC:11344]
Coordinates
chr24:1578035-1579385:+
Coord C1 exon
chr24:1578035-1578163
Coord A exon
chr24:1578528-1578714
Coord C2 exon
chr24:1579111-1579385
Length
187 bp
Sequences
Splice sites
3' ss Seq
CTTCTCCTTCCTCACCCCAGACT
3' ss Score
8.99
5' ss Seq
CCGGTAGGT
5' ss Score
9.39
Exon sequences
Seq C1 exon
CAGCCCAGTCAACAGTTGCCTGCAAGAGCTACACGTACAAATGCCGCAATGGGCTCTGCATCAGCAAGCAGAACCCGGAGTGTGATGGGCAGAAGGACTGCGAAGACAATTCTGATGAGGACAATTGCA
Seq A exon
ACTGTGGGACCCGCTCCTACATTAAGAAATCACGGATCGTCGGTGGGCAGAACTCAGATGTGGGAGAGTGGCCGTGGCAGGTCAGCCTCCATGCCAAGAGCCAGGGCCACGTCTGTGGAGCTTCACTCATCTCAGAGACCTGGCTGGTGTCAGCAGCACATTGCTTCCTGGAGCTGCAAGGCATCCG
Seq C2 exon
CTACTCAGACGCCAGCCTGTGGACAGCCTACCTGGGCCTGACCAACCAAAGCAAACGCAACGATGCCAACGTGCAAATGAAGCAAATCAAGCGCATCATCTCCCACCGTTCCTTCAATGACTACACCTACGACTATGATATTGCTGTGATAGAGCTGCAGAGCCCCGTCACCTTCTCCGCTGTCGTCCAGCCCATCTGCCTGCCCGATTCTACGCACAACTTCCCCGTGGGCAAAGACCTGTGGGTGACCGGATGGGGAGCGACCGTGGAAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001331_CASSETTE3
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
PF0005713=Ldl_recept_a=WD(100=86.4)
A:
PF0008921=Trypsin=PU(21.3=79.4)
C2:
PF0008921=Trypsin=FE(39.1=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TACAAATGCCGCAATGGGCTC
R:
GCTCTGCAGCTCTATCACAGC
Band lengths:
257-444
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]