Special

RnoINT0096378 @ rn6

Intron Retention

Gene
Description
myosin heavy chain 11 [Source:RGD Symbol;Acc:3136]
Coordinates
chr10:800444-801658:+
Coord C1 exon
chr10:800444-800536
Coord A exon
chr10:800537-801594
Coord C2 exon
chr10:801595-801658
Length
1058 bp
Sequences
Splice sites
5' ss Seq
TTTGTAAGT
5' ss Score
7.4
3' ss Seq
ACTTGTTCTTCTCTTGGCAGGGC
3' ss Score
10.07
Exon sequences
Seq C1 exon
GGGGAGCTGGAAAAGCAGCTTCTACAGGCAAACCCAATCCTGGAGGCTTTCGGCAATGCAAAAACTGTCAAGAATGACAACTCCTCCCGCTTT
Seq A exon
GTAAGTAGCAGAGCCATATGGGCTTTTCTGGGACTGAGTGGCCACCCAGTGTCATATATCCCCTAAGAACACAGACTCTAAGAGTATAAGGAGAGTTCTGACTAAAGGACTAGAGGCGATAGAGGATAGCCATATATGCTCCCTGTCTTCCAGTCCTCACCCAACATTTAACATTTGTGATTTATCTAACATTTACTGAGCACCTAGACAATGTTAATACTCATCCATACATTCAACAAAGCATGAACTTCTCTATAGTACATACATCTGTCCACTACCAAATATTGACTATGCACCAACTACACAGACTCATTCTGGTGAACACTTTTTATAGATCGTTCCCTCCCATTTTAATTTTTGAGTTGGTTTTTTATTAAGCACACAGACCTAGGTACCAAAAATCACAATGAATAATCCAATGTGGCTCCAGACACAGAAAGAAGACCTGCTTTGGGGAGCAGCAGCCAGTGAGGACTGCTGTAAACCCAAGGTCCTGAACCTGTAAGAAGAAAAACCAAGACATGGTGACATGTGCTTACAGTCACAACACTGGGGAAGCAGAGACAGGGTAATCCCTGGAACTGCCTGATCAACTAGCCTAACTTGCCTAGAGAGTTCCAGGCTAGTTAGACTGGTAGTGTGTACCTCAAGTCCCCACCCCCTCACCCCCCCACCCTTGCTACCATCACACACACATGAACAAACATTTCAGTCTCTCACTGCTCAGGCCAGACCTTGGTGTAGAAAAGCCTGTGACTGACTGAAGAGCAACATCCTGCCAGGCCACTTAACCTATGTCAACCTCACTTTCTCTACCACATAGAGACAGCCATGAAGGACTTAGTTGTTTCTTGAGATGATGATGTTTCCTGCATGGGTTTGGGAGGCTTCGGGAGGGGGTGTCCCAGCTCAGATGCTGGTTGTTGTGGACTGTGAAGTTCTGAGTCCTTTCAGAGTCTCTCCTGCCTCCACGGGGCGCCTAACACTTCCTCACTTGCCTGTGGTGTGTAGGGTCTGTGCTGAGCCTGGCCCACATTGACTTGTTCTTCTCTTGGCAG
Seq C2 exon
GGCAAGTTCATTCGCATCAACTTTGATGTCACTGGTTACATTGTGGGTGCCAATATCGAAACAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000057880:ENSRNOT00000084608:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0006316=Myosin_head=FE(13.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(3.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
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]