Special

GgaINT0129035 @ galGal4

Intron Retention

Gene
Description
myosin, heavy chain 13, skeletal muscle [Source:HGNC Symbol;Acc:HGNC:7571]
Coordinates
chr18:309018-309618:-
Coord C1 exon
chr18:309229-309618
Coord A exon
chr18:309145-309228
Coord C2 exon
chr18:309018-309144
Length
84 bp
Sequences
Splice sites
5' ss Seq
AAGGTTAGA
5' ss Score
6.12
3' ss Seq
TGCTTTCTGTGTCTTAACAGAGC
3' ss Score
11.08
Exon sequences
Seq C1 exon
GCTCGTACAGAAGAATTGGAGGAGGAAATTGAGGCTGAACGTGCAATCCGTGCAAAGACTGAAAAGCAGCGAGCTGACCTCTCCAGGGAGCTGGAGGAGATCAGTGAGCGCCTGGAGGAAGCAGGAGGGGCTACAGCAGCTCAGATCGAGATGAACAAGAAGCGTGAGGCAGAATTTCAGAAGATGCGCCGTGACCTCGAAGAGGCCACGCTGCAGCACGAAGCCACGGCTGCTGCCCTGCGGAAGAAGCATGCGGACAGCACAGCGGAGCTTGGGGAGCAGATCGACAACCTGCAACGTGTCAAGCAGAAGCTGGAGAAGGAGAAGAGTGAGCTGAAGATGGAGATTGATGACTTGGCCAGCAACATGGAGTCTGTCTCCAAAGCTAAG
Seq A exon
GTTAGATTAAATATTTCTCACCACTGCAGTCATTTTTCTGAACAATTAAATGAGCTGATAGGTATGCTTTCTGTGTCTTAACAG
Seq C2 exon
AGCAATCTGGAAAAGATGTGTAGAGCTCTCGAAGACCAGTACAGTGAAGTCAGAACTAAAGATGATGAGCATATGCGGCTAATTAATGATATGAACACACAGAAAACACGTCTACAGACTGAGAATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000000779:ENSGALT00000001184:25
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=0.953
Domain overlap (PFAM):

C1:
PF0003816=Filament=FE(50.6=100),PF0157614=Myosin_tail_1=FE(33.6=100),PF123293=TMF_DNA_bd=PD(50.0=30.8),PF131661=AAA_13=PU(18.0=35.4)
A:
NA
C2:
PF0003816=Filament=PD(10.2=60.5),PF0157614=Myosin_tail_1=FE(10.9=100),PF131661=AAA_13=FE(16.4=100),PF059116=DUF869=PU(25.6=46.5)


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:
CTGCAACGTGTCAAGCAGAAG
R:
AGCCGCATATGCTCATCATCT
Band lengths:
179-263
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]