Special

GgaINT0015070 @ galGal4

Intron Retention

Gene
Description
myosin-11 [Source:RefSeq peptide;Acc:NP_990605]
Coordinates
chr14:7571868-7572665:-
Coord C1 exon
chr14:7572542-7572665
Coord A exon
chr14:7572040-7572541
Coord C2 exon
chr14:7571868-7572039
Length
502 bp
Sequences
Splice sites
5' ss Seq
AAGGTAATA
5' ss Score
8.49
3' ss Seq
TCAAATCTTTACTTTTTCAGTGC
3' ss Score
8.15
Exon sequences
Seq C1 exon
GAAAGAAAACTTCTTGAGGAAAGAGTAAGTGACCTAACAACAAATCTTGCAGAAGAGGAAGAAAAAGCCAAAAACCTTACAAAGCTGAAAAACAAACATGAATCCATGATTTCAGAACTGGAAG
Seq A exon
GTAATACAAAGATGCTCTGTGTCAGATATTTGCTTTGGTACATATAAAAAATAAACAACAATAAAACCCTAAAGAGAATCTGGAGTGAACTTCTAAAAACTATGTTTTCCAATTTCATATGCTGAAACCATTTTGTGAATGACAAATACTGAAACCCCAAGATGCATAAACCATTGATAGCTTTTCTTTATATATATAGAGGAGAGGAGAGGTAGTTGGGGGAAAAAAGTGTTTCTGGAGATATAATATATATATATATATATATATATATATATATATTTAGTGGCTGGAAATAAGTGATGATAGCAAGGTACTGCATGTTGCTTCAGAAAGACAATAACTCACACTCACTGAATATTACATATATCACTTAATTATCACACATATATACATAATATCACAGCCTTACTGAAGATGAGAACATTTTTGCATCCAAGTTCAAGATCAGATGAGTGCTCCTTGCACTAACCCACTCTCATGACTCAAATCTTTACTTTTTCAG
Seq C2 exon
TGCGACTGAAAAAGGAAGAGAAGAGCAGACAAGAACTGGAGAAAATAAAGAGGAAGTTGGAAGGAGAGTCAAGTGATCTGCATGAGCAAATTGCAGAGCTCCAGGCACAAATTGCTGAGCTGAAGGCACAGCTAGCCAAAAAGGAGGAAGAGCTGCAGGCTGCTCTAGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006520:ENSGALT00000010534:25
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.857 A=NA C2=0.603
Domain overlap (PFAM):

C1:
PF0003816=Filament=PU(3.4=19.0)
A:
NA
C2:
PF0003816=Filament=FE(23.9=100),PF093045=Cortex-I_coil=PU(48.4=75.9),PF0157614=Myosin_tail_1=PU(2.9=43.1)


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:
AAAACTTCTTGAGGAAAGAGTAAGTG
R:
CCTGCAGCTCTTCCTCCTTTT
Band lengths:
278-780
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]