Special

RnoINT0096570 @ rn6

Intron Retention

Gene
Description
myosin heavy chain 7B [Source:RGD Symbol;Acc:1307994]
Coordinates
chr3:151128568-151129316:+
Coord C1 exon
chr3:151128568-151128711
Coord A exon
chr3:151128712-151129159
Coord C2 exon
chr3:151129160-151129316
Length
448 bp
Sequences
Splice sites
5' ss Seq
TACGTGAGC
5' ss Score
4.3
3' ss Seq
ATTGTGAACTCTCTCCTCAGACA
3' ss Score
8.28
Exon sequences
Seq C1 exon
GTGCTGACAGTGCGTGAAACGGAAATGCAGCCCATGAACCCACCCCGCTTCGACTTACTGGAGGACATGGCCATGATGACGCACCTCAACGAGGCTGCAGTGCTGCACAACCTGCGCCAGCGTTATGCTCGCTGGATGATCTAC
Seq A exon
GTGAGCCCCGGGCAGGGACGGCTCAGCGGTGGGCGGGGCCACTAATGGGCGGGGTCTAAGGGCCCGAAGGAATGGCGTCTGGAGAGCTAGGCTAGAGGGGAGTTGGAAGTGAGCTCTGGGGCTGAAAGAGCAGAACTGAAGAGTGGCAAAGGAGAGGGCTAGAGGAACAAACTGTAGGTAAATGAGGGAGCGGCCTAGAGCGATGACTTGATGATGTCTAGGGTCTTGGAAGCAGAGCCAGGACCGTGTATGGGGCCTAGCTGCCTACTTGGCACCTCTGAAGGGTCGGTAAAGGGTTCTGTGGCTCAGGCTGGAACAGGAGAAAGGACTTTGCATAGGATATCTGGAGGCTTTTTGAATATTGCAGGGGTCATGGTGGGCCTGGGAATAGGAACTTGGACATCTTTCTTCCCGCCCCCAAAAGCTCTATTGTGAACTCTCTCCTCAG
Seq C2 exon
ACATACTCGGGCCTCTTCTGTGTCACCATTAACCCATACAAATGGCTCCCGGTCTACACAGCTACTGTGGTGGCCGCCTACAAGGGCAAGCGCCGCTCGGAGGCCCCGCCTCATATATATGCAGTGGCAGATAATGCCTACAATGACATGCTCCGCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000018997:ENSRNOT00000025859:3
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.146 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0273614=Myosin_N=PD(16.3=14.6),PF0006316=Myosin_head=PU(4.1=58.3)
A:
NA
C2:
PF0006316=Myosin_head=FE(7.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGACAGTGCGTGAAACGGAAA
R:
CGGAGCATGTCATTGTAGGCA
Band lengths:
295-743
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]