Special

GgaINT0041857 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr6:28915490-28916188:-
Coord C1 exon
chr6:28915877-28916188
Coord A exon
chr6:28915643-28915876
Coord C2 exon
chr6:28915490-28915642
Length
234 bp
Sequences
Splice sites
5' ss Seq
GATGTAAGT
5' ss Score
9.11
3' ss Seq
TATATGTTTCATTCTCTTAGGTA
3' ss Score
9.19
Exon sequences
Seq C1 exon
TACAAATACAGAGAAGCCTTCCTTCGAGACAGAGGCCAGAGGATTGGATTCTTCAGTGCAAATGATGATGCCCACACCAGACATGTCCTCAGAGTAGGGAAACTCCAGAGCGACAACCTGTACAGGAGCGGATACGCCCAAAACAGAGGACATTTTCAGAGTCACCTTAACCAGCCTGGGTTCCTCCATGCTAAGAGAAGCCAGCAGCTTGCCAGCAATGTTAACTACAAGCAGCCCTTGCACCAATACACTTGTGATCCTGAGCAGCTAAATGTGAAACATGCAAAGCAGGCCTATAAGCTGCAAAGCGAT
Seq A exon
GTAAGTACAGCTGAGAGGTACTGTCCTTCCCAGTGCTAAGAGCTGTCTGTGTGGCAGTGTCATCACAGACCTTATTTATCAACAAAATCATCCTTAAGAGATCTACAATCTGTTTGCAGAAAACACAATTTATTTGTTTACTACTGAGCCTGTTCCTCTTTCTATTCTCTCTCTCAAAAACACAGAACATGCGGTTAATAGTAACACGTGCTATTATATGTTTCATTCTCTTAG
Seq C2 exon
GTAAAATACAAGTCTGACCTGAACTGGCTCAGAGGCATTGGCTGGACTCCTCCAGGTTCTTACAAAGTGGAAAGGGCAAGAAGAGCTGCTGAGCTGGCGTACCTTCGGGAAATGGGGTTGCAGGCTGCTTCTGCTCAGTATGGACCTGAAGCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000008914:ENSGALT00000014498:36
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.106 A=NA C2=0.146
Domain overlap (PFAM):

C1:
PF0088013=Nebulin=PD(37.9=10.6),PF0088013=Nebulin=WD(100=27.9),PF0088013=Nebulin=WD(100=20.2),PF0088013=Nebulin=PU(55.2=15.4)
A:
NA
C2:
PF0088013=Nebulin=PD(37.9=21.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCAGAGCGACAACCTGTACA
R:
AGCAGCTCTTCTTGCCCTTTC
Band lengths:
299-533
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]