Special

GgaINT0127797 @ galGal4

Intron Retention

Gene
Description
myosin, heavy chain 1A, skeletal muscle (similar to human myosin, heavy chain 1, skeletal muscle, adult) [Source:RefSeq peptide;Acc:NP_001013414]
Coordinates
chr18:436927-437518:-
Coord C1 exon
chr18:437400-437518
Coord A exon
chr18:437124-437399
Coord C2 exon
chr18:436927-437123
Length
276 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
AAACACTCTTGTTACTCTAGGCC
3' ss Score
6.42
Exon sequences
Seq C1 exon
GTGAATATTCACGACAAGTGGAGGAGAAAGATGCTCTGATATCTCAGCTGTCTCGAGGCAAGCAGGCATTCACCCAACAGATTGAGGAACTCAAGAGGCATTTAGAGGAGGAGATAAAG
Seq A exon
GTGAGGACGTTTTCCAAAATTCTGTCTTATCCAGTGGATTTTCCTGACTAAGAGGTGCTTCAGACAAGCATTTAATGACAGAACTAGTATGATGACATAGATGAAAACAGTGTGACTCTCCATGTTAGCTCTGCTGCTTTTCATTGTTCTTGTTGTGAATACTCAACACTTTCTTCTTCCTTGAAAGGACTTTTTTAATTTCATAAAGAAACAATTTTTGAAAACATTTCAGTTTGAAAGCTTCCATTCATTTTCCAAACACTCTTGTTACTCTAG
Seq C2 exon
GCCAAGAGTGCCCTGGCCCACGCCTTGCAGTCAGCCCGCCATGACTGTGACTTGCTCCGGGAACAATATGAGGAGGAGCAGGAAGCCAAGGGTGAGCTGCAGCGTGCCCTGTCCAAGGCCAACAGCGAAGTGGCCCAGTGGAGAACCAAATATGAGACGGATGCTATTCAGCGCACAGAGGAGCTGGAGGAGGCCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000026748:ENSGALT00000039878:30
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.250 A=NA C2=0.424
Domain overlap (PFAM):

C1:
PF0003816=Filament=PD(4.9=35.0),PF0157614=Myosin_tail_1=FE(4.5=100),PF0003816=Filament=FE(12.5=100)
A:
NA
C2:
PF0157614=Myosin_tail_1=FE(7.5=100),PF0003816=Filament=FE(20.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CACGACAAGTGGAGGAGAAAGA
R:
CTCCTCTGTGCGCTGAATAGC
Band lengths:
293-569
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]