Special

GgaINT0130575 @ galGal4

Intron Retention

Gene
Description
myosin XIX [Source:HGNC Symbol;Acc:HGNC:26234]
Coordinates
chr19:8131683-8132437:-
Coord C1 exon
chr19:8132330-8132437
Coord A exon
chr19:8131754-8132329
Coord C2 exon
chr19:8131683-8131753
Length
576 bp
Sequences
Splice sites
5' ss Seq
GAGGTAACT
5' ss Score
8.77
3' ss Seq
CAACTCAATTTGTGCCTCAGGTT
3' ss Score
6.33
Exon sequences
Seq C1 exon
AGTTCACTTGAAAATCTCATGCAGATCTTGAACAGCACCGAACCACATTACATCCGATGCATCAAGCCTAATGCTGACTGCCAGGCAATGACTTTTAGAAAAGAAGAG
Seq A exon
GTAACTTCTCCATAAGCTTTCTTTACTACCTCAGAAGCTTCCCAGAAATAATGTGCAGGGCTTTGCACTGAGTCTCAGGTGGTTGTGATTCACTTGTAAATCTCTTTTCACAGTAGATTTGGAAAGAATGTTTTCTTCTTTGAAATTTCCAAGATAAATGTCCTTTCAGAATCAATGATGAAGCGTGTCTAAAATGGCACTGGTAAGCTCAGCAGCTCATTCAGATGCAACTTACTTGTTGCTGTATGGGAAATCATCTTACCACAGTGTTCATGGGTTATTTGGTATGATAGCTTCTCAGCTCATGAAGTAGATAAAGCTCATCTGGCTGTGGCTACCCTGGTCACAAAGATAACTTCACAGTGCAAACCCACAACAAAAGTCTGCTTGGGTATTAGAAAATGCTAACTAGCTGTGTAATCCCCTTCTCCACTCTCGCCATTTGTTCCCTAACCACCAGTGTGGTGGCTGAGCAGAGCTGAACGTGGCTTGGATTGAGTGCATGCCATGCACACCTTCACTGCAGCTTCCACAAAGAACAAGTGTTTTCCTAAAACAACTCAATTTGTGCCTCAG
Seq C2 exon
GTTCTTAGCCAGCTTCAGGCATGTGGAATAGTTGAAGCCATCACCATCAGCGCAGCAGGCTTCCCTATTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005374:ENSGALT00000039165:17
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:
PF0006316=Myosin_head=FE(5.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(3.3=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]