Special

RnoINT0096349 @ rn6

Intron Retention

Gene
Description
myosin heavy chain 11 [Source:RGD Symbol;Acc:3136]
Coordinates
chr10:819510-822189:+
Coord C1 exon
chr10:819510-819703
Coord A exon
chr10:819704-822067
Coord C2 exon
chr10:822068-822189
Length
2364 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGG
5' ss Score
7.13
3' ss Seq
TCACTGGCCTCTTCCCACAGTCT
3' ss Score
9.61
Exon sequences
Seq C1 exon
TGGACCGCATTGTGGGGTTGGACCAGATGGCCAAGATGACTGAGAGCTCACTGCCCAGTGCCTCCAAGACCAAAAAGGGCATGTTCCGCACCGTGGGCCAGCTCTACAAAGAGCAGCTGGGGAAGCTGATGACCACACTGCGCAACACCACGCCTAACTTTGTGCGCTGCATCATCCCCAACCATGAAAAGAGG
Seq A exon
GTGAGGCATGTCCTAACCTGGGCCTCCTGCCTATGGGATAGTGCTGGCATGGTGTGGCATGGGGGGGGGGATCTATAGAGAGGAACCGGGGAGACAGCAAGGTACACCAATGAGGTAGACAGGCAGAAAGAGAGGTCTGACCTTGGTTCCTGCCCTGAGTGTCCTCAAGGAAGTCCTGCACCTGGAAAGTTATCTGGATTTGGGCCTATTCCTCATGCCTGAAAGCAAAGGACAGCAAGGAAGGAAAGAAGGGATAGAGGGAGGGAGAGGACAAAGGAGGGAGGGAGAGAACAAAAGAGAGAGGGAGGGAAGAATGAGGGGAATCTTTCCAGAGAATGTTCAGCCAGTTAGAAGCATGAGGTGTGAGGCCACCAATCCTTCCACTCTTCCAGTAAATGCATGCCAAGCTGCCACACAGTGTTGAAGAAATCACTGGAAACACATTTGCTTGTCACAATGGGAAGAGGATTGCTACAACATCTAGTAGAGAGAGACCAGGAAAGTTGAGGGACAGCTCAGTATGTTCCCACAACAGAGAATTAGTGGGCCCAAAAATGTCATTGATGCTGAGGTTATGAGAGATCACAGGGACCTTGACACATAGGCTAGAAACACGATGGTAAATTTGGAAAATAGCAAAAAATCTGGGCTAGCTATCTCTGCCTCAAGAACTTTAAGAATGGGTAGATGGTCTGGAGAGATAGCTCAATGGGTAAAGGCTCTTGCTGCCAAGGCTAAACCTGAGTTCCATCCCTGAGACCCACATAATAGAAGGAAAAACTGACTGCAGCAGGATGTCCTCTGACCTTCACATATGTACTATGGCATAGCTGTGCCCATACTTACCCCATATACAACATAAATAAATAAATGTCATTTAAAAAGGCATGGGTATCATCAACCTGGTGAACTGCATAGTGGGGTATGAGTTTTAAGCCAAGATCTCGATAAGAAAATGCATAGAGGTGAGAAATTAAGTCTAGGCAAGAAAACTATAGCTAGGTAATTTTGTATTGCTTTTGTTTGTGTTTGTGTGTGTACATGTATGTGTGGATGTGGGGTATACATACACAGTGTACTATAGAGGTTGGAACACAAGCCCTGGTATCACTCCTGAGGTGCCTTCCACTCTGTGTGGGCCAGCTTTCTTACTGGCCTGGAGCTTTACCATGCAGAGCTGTTGAGCTGGTCTATGAGCTTCTGCAATTCTCCTGTCTCTGCCTCCCTTCTTACAGCTCTAGAATTATAGGCCCAGGCTATGCCCAGCTTCTTCCATGGGCTGCATGAATTGAACTCTTCTGGGTCTCATGCTTACAAGGCAGGCACTTGATGGATGGAGGTATCCTCTCAGATACTTTGTTTCATATGAATACAAAAAGGTATTAAATAGGGATGGGACTATAATAGCTTATGGAGTTCCTTTTATGATAGCTGGAGATTGGCATCCTGTCTGTAGGAAACTACTTGAAGGAGTTTAAGCAGTAGGTCATGAGCAAAATTATCTTTTCGACCAAATGAGTTAGAGGAGGCAGTCAGGGCTGAGGGGAAATGATCAAGTTAGAAGGTGCACTTGTCTGGGCAGAGGAGACAGACAATGGCCTAAAAAAGTAGGCTGGGGAGATGCCTTAATCATTTAAAGTTCTTGCCACACAAGTGGGACTTGGAACCCCGGAAGCCCACATAAATACTAGGTGGGTATGGTAGCCCACTTGTAACTTTAATCTCAAAAGACAGAGACAGGGAATCCCCAGAATTCCAGCCAAGAAACTAATGGTACTGGAGACCTTTGAATTTGAGTGAGTGAATGAATGAGTTAATGAATAAGCTAGAAGAGTGATTGAGAATTATGTCTGACACCAATTTTGTGCATCCAAATGTGTACAAAAACATATGAACATACAGACATCACACAATGCACATCCACATCACATCCACAAGCACATTTTACATATGTACATGCATCACACACATCATGTACACATACACGTTTGAACATGTGTGCTCTTGTAGACATGCAAAAACATGAATGTATACATATGTACACCACATCTGTTTTTGTTTATATTTTTGTTTGTTTTTTTTAAAGAAACTTACTGGGGAAGACATGGGAGGCAAGAGCTAAGGGTGGTGATGGCCCAGAAGTAAGGGAGAGGGTAGTGAGGGAATAACAGCTTCAGCTTTTAGCCAGGGATATTGGCACCACCAAACACAATGGAGATTATAAGAAAAATAGTGCCAAATTGTGAAAACCCACACTGGTAATAATGCACACTGTCCCTCAGCTAAACCCTGTTAAGACCCTACAGACTGCCAGGTATGCTTTCTGGCAGGGCTCCTCCATTGATCACTGGCCTCTTCCCACAG
Seq C2 exon
TCTGGCAAGCTGGATGCATTTCTAGTTCTGGAGCAGCTGCGGTGCAATGGTGTGTTGGAAGGCATCCGCATCTGCCGTCAGGGCTTCCCCAACAGGATTGTCTTCCAAGAGTTCCGGCAACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000057880:ENSRNOT00000084608:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.044 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=PD(0.4=15.4)
A:
NA
C2:
PF0006316=Myosin_head=FE(5.8=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
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]