Special

GgaINT0107552 @ galGal4

Intron Retention

Gene
Description
signal peptide, CUB domain, EGF-like 1 [Source:HGNC Symbol;Acc:HGNC:13441]
Coordinates
chr1:68732170-68733755:-
Coord C1 exon
chr1:68733663-68733755
Coord A exon
chr1:68732287-68733662
Coord C2 exon
chr1:68732170-68732286
Length
1376 bp
Sequences
Splice sites
5' ss Seq
CAGGTAGGT
5' ss Score
10.28
3' ss Seq
TTTTTGTTCTACATCAACAGATT
3' ss Score
8.56
Exon sequences
Seq C1 exon
ATTCAGAGAACAGCTACACGTTGAGCTGTGGTGTTCCTGTCCAGCAAGGCAAGGCTCAGCAGAAGCGCAATGCCACCCTTCCCAGCTGTGCAG
Seq A exon
GTAGGTGCTGTCCTGCCCACCTCAGCTGTGGCCTCTGGGAGATAGGTAATGGAGGTCTCCTAAACCACTGAGGAGATGCAAGATAGACAGCTCTGAAGTAACACAAGGCCAGATTTAAGAGTTATATTCCACAAGGGCAAGCTCTGGAGTAAATTACTTTCCACAGTCCAGAATCTGACAGCGAGCACATAAAAATGGCGGTTCTTCACAGACGAGGAGACGAGAAGCCCAGCAGGACACAGCAGCCAAAGGCAACAGCGCTGCCCGGTGGTCAGCTACAAAGACCTCGCTGAGGATCGTGGAGGCTCTAGGCATTGCATTTCTATAACCAGAAAGGTTACAGTATTTTTATGAGCACATTTAGTGTTTCATTCGTCTTGTTCACAGAAGTGGCTGGATTATTTTGCAGAGACATTTCAAAATTTCAAAGGTGATACTCAGAATAAATTAAACTCAGCTCTAGCAGATGAAGTCTGGCAAAATTGAAAGTTGAAACAGCATCCAGCGGAGGGAACTATCAGCCCATTTTACATATCAATACCTGCTATGCTTCTCTCCAGTTTCCTTGTTCTCTAGCCATGTACTTGTTATATGTTTGGAATGCAATACGAAGTATGATGCTGTGGAGTTAACACAGCAGACCATCTGTCTGCCTGTGCCACATGGGCAAGTAACCTCTATAATGCTTTCAGGGTTGCTCCCCATTGCATCACTTACTTGTAATACCCTTTTACTTGCTCCAGCTCCAAGCTTCCTGCAGGAGCAGGAAGGTGACAGGCCATGCCATATCTTTTACACCATGGAATTTGTGAGGAAGTCAGTCAGCAGTTGCATTTTTTAAGCACTGCATACTTTGGAGCCTTTAAAGTTACGACTGGCTTGGATCTAAAGCTGAAGAAAAAATCTTGCAAGCTATAGACCACCATCAAATAAAGGTATTTCCTTTGGATAGTTTTCCATTGTCAACAGTTTAACTTCATTGAGTTAGTCTTACTACTGGTTGGCATTAGCAAGAGCAGAGACACAGCCAAGTAGCATAGGAAGTCACAGAGTCAGAAAAAAAAACGCTATCAGTGAATCTTTCTCATAATAAATGGCAAATTCACCCAAATCCCACAAAGATGTGCAGGCGTACTGGATGGAAGGAGTACATGCAGAGCGTGTGCAATACTGGCGAATTCATTGATCTGTCTGGGCTCAAGAGTAAGTGCTCATGGGAAATAATAAACTTATGCAAATGGATGCCTGTATAGGTCTTGGCCTGTGTGTTTTCTGTGTTGCAAAATGTCTTTTGAGTCTGTTTTCAAAAATAAATTTCAGGCTTAATTTCATCTGCATGACAAACAATGGCTTTTTTTTTTGTTCTACATCAACAG
Seq C2 exon
ATTCCTTAGCCCCTCCAATCAAGCAGAAAGCTCGTTTTAAAATTAAAGATGCAAAGTGCCACTTACGGCCTCGCAGCAAAGAAAAAACAAAAGATGCTGGGAAGCAAGCTGTGTTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000014178:ENSGALT00000022933:12
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=0.225
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


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:
AGAGAACAGCTACACGTTGAGC
R:
CTAACACAGCTTGCTTCCCAG
Band lengths:
206-1582
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]