Special

GgaINT0115697 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr1:181404275-181405731:+
Coord C1 exon
chr1:181404275-181404400
Coord A exon
chr1:181404401-181405681
Coord C2 exon
chr1:181405682-181405731
Length
1281 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAGG
5' ss Score
9.33
3' ss Seq
TTGTGTTTTTTACCCTCTAGGTC
3' ss Score
11.68
Exon sequences
Seq C1 exon
GCAATAGCAGTTGAGAGCGCGAGTGTGTTGGTGCACTGCTCTGATGGCTGGGATAGGACGTCCCAAGTTTGTTCTCTTGGAGCTCTCTTGTTAGATTCCTATTACAGAACAATCAAGGGGTTCATG
Seq A exon
GTAAGGAAGCTGTTGTATTGTTGAATTGTTTCTTGCTAAATCAAAGAATGTAAAATGTTTGTGTGGAAGTGCACAGAGTAACTGAAGTGATGTTTGTTTTTTCTAATTACAAATATGGTACCATATCTGCAGAATTTGCGTTAGAAATAGTTTACAGTAGGGAAGCACTGTGCATTTAAAATAATATAAGAGACTGAAATACAAATAGCAGATTGTTTTAGGCACCGTGTGGAAATGCAGTAACTGCCTCTTTGATCTAAAATAACAAAAAGCTTACCTCTGAAATGCAGGCATTCTGAAGTGCTTATGAGATAGACAGACTAAATTCTAGCAGCTATGCACTTTCATTATTTGTCCCAAATCAACATCACTAAAATCTGAATGACATCCCTTCCACACAGCAGCACAGAGACCTGAACATATCTGAGCAACCTAAAGTACTTCATCCTCCTCGTGAGAGAAATGAAGGATTTTAGTGTGGTTATTTAAAATTTCAGAGTAGAAAGATGGACTTTGTCTTTGACATGGCTTGGTGTTATGGGAACACTTCAGTTAACACACGAATTGCATTCCATGTATTCATTACAGACTAACTGCCACAAATAATACAAGCCGCAAAAGCTAGAGTGAGAAGGAATTGGTGGATTAACTAATCATGGATAGTGGGAATGTCAGTAATCTTTAAGGACCTCATCTAATCAGTTATTTTACTTGTCCTTAGTCCTCGCTTTTGATTGGAAGTTTTGGGAAACCTTCTGCAATGAGCAATCAGTCCTCTGCTCTTTTTAGTGCTCGATATTCCAACTGGAGTGATAAAACAAGCTAGTGTTGATATTAGCAATTTTACTGCTATAAAACGTTAAGATGAAATTGTGTGATTTAATGGAAATTGTAATAGCAGGAGTGCAATACTAAACTTCTTCCCATACACCGCAGTTAATTTTTTGTAAATTGATAATTCATTTATGTGACTGCATTTAGATGTGAAACTGTGCAGTATTCATGTGCTTAAAGTATGTCAGTTCTAACAGTAGGTGTCTGATTGTCAGCCTGTTCAGCTCTTCTTACTAATTTTAGAAATACGACTTGCACATCTCGTGTAGGAAAGAAAAAACCTTCCAGGAAATGAAGGAACTGTGAAATGATACACAATTGCTCCTACTGTAGTTAAATTGAGTCGGATTTAAAATACGGTACATTGATAACCTGTGAGGTTAATTCTGCGGGGATGCAAGACTTAGTACAACTTTGCATTAATGTTTTGTGTTTTTTACCCTCTAG
Seq C2 exon
GTCTTGATAGAGAAAGACTGGATTTCTTTCGGGCACAAGTTCTCTGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000017112:ENSGALT00000027648:9
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:
PF066029=Myotub-related=FE(12.0=100)
A:
NA
C2:
PF066029=Myotub-related=FE(4.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
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]