Special

GgaINT0000976 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:253902-254592:+
Coord C1 exon
chrE22C19W28_E50C23:253902-253959
Coord A exon
chrE22C19W28_E50C23:253960-254541
Coord C2 exon
chrE22C19W28_E50C23:254542-254592
Length
582 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGT
5' ss Score
11.45
3' ss Seq
AACTTGACTTTTCCCTCCAGGCA
3' ss Score
9.1
Exon sequences
Seq C1 exon
GTGGAGATTTACGTTCTATTTAAGTATATTTCTTTATGGAATCAGGTTTCTCTGGACG
Seq A exon
GTGAGTTGATCTGGCACATCCCTCTGCACCCTCCCACCTGGTTTTTCTGTGTGTTGTGCCACTGAGTTAGCACTGCAGTGCTGAAATTTCAGGGCTTTGACTACAGTGACCCTTCTGTTCTCCCACCTAGCTTCAAACGAGGGGAATTTAGTGATAGTCACCTCCATGTACCCTTATTTGAGATCCTGGAGTTTTTATTTAAAGGCCACTTTGACAGTATGAGAAAGTTTCTAAACAAATCCGTCATTATGGAAATGCTAAAAGTTTGTTTGTTCTTTTACACCAGAATAGGACAGACCTGCTTTCTTGGTGTGGAGAGGTTTTGTTTTCTTCCCATAGGAATACGCATTTATCTCTGAGTCTTTATTATTAGAGCTGCCTACTTATTCTTTGAATTTCTGCTGCATTACAGTTTGCCTTTGGGTGCAGAATGATTATTTCAAATCATTATTATGTCTTACAGTAAATTTAGCTTGGAACAAAGGTAAAATTTCAGTGAACTGTTCAGTGTATTCGTTGATGCCTTAGATAATAGGGAATTAAAAAGACCAGCAGAATAATAAACTTGACTTTTCCCTCCAG
Seq C2 exon
GCACCCTGGTTTTGGGACACACGACAGTGCTGGTACAGCTACCCCTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006184:ENSGALT00000009980:4
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:
PF0379811=TRAM_LAG1_CLN8=FE(9.8=100)
A:
NA
C2:
PF0379811=TRAM_LAG1_CLN8=FE(8.2=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]