Special

HsaINT0107511 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 11 [Source:HGNC Symbol;Acc:HGNC:7569]
Coordinates
chr16:15741760-15745237:-
Coord C1 exon
chr16:15745129-15745237
Coord A exon
chr16:15741892-15745128
Coord C2 exon
chr16:15741760-15741891
Length
3237 bp
Sequences
Splice sites
5' ss Seq
AAAGTGAGT
5' ss Score
8.4
3' ss Seq
GGCTAACCGTGTGTGTGCAGGTG
3' ss Score
6.66
Exon sequences
Seq C1 exon
GGCTTTTGCCAAGAGGCAGCAGCAGCTGACCGCCATGAAGGTGATTCAGAGGAACTGCGCCGCCTACCTCAAGCTGCGGAACTGGCAGTGGTGGAGGCTTTTCACCAAA
Seq A exon
GTGAGTGCTCTGCCCCAGCCCCCTTCCCAGGGGCCCCCAGCCCTGCTTCTTCACTCTGGAGCCTTCACATTTGGGACAGGAGGTGGTCGCAAGTGGGTGTGGAATGGAGGGCTCGAACTCAGACCTTGAGCATTGGCGGTTCTCTGGCCCGAGGAGGCCCTGTCCTTTGGCACATAGGCTATAGCCAGGACCTTAACACAAAGTATTAATATTTCCATCCGCACTGGAATCCCTCGTGTGGCCCATTTATAGCCACACCCACTTCCTCCGTAGCCATGGAAACCACTCTGTTCTCCAGTTCTGTAATTTTGATGGTTCAAGAATGCTGCCGGGGGCGGCGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCAGGCGGATCACTTGCGGTCAGGAGTTCAAAACCAGCCTGGCCAACATGGCAAAACCCTGTCTCTACTTAAAATACAAAAATTAGCTGGGTATGGTGGCAGGCACCTGTAATCCCAGATACTCAGGAGGCTAAGGCAGGAGAATCTCTTGAACTCAGGAGACAGAGGTTGCAGTGAGCCAAGATCATGCCTGCACTCCAGCCTGGGTGAAAGATTGAGACTCTGTCTCTTCTTTCTTTTTTTTTTTATTTAAAAAAAAGGCCAGGCACGGTGGCTCACGGCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACAAAGTCAAGAAATCAAGACCATCCTGGCCAAGATGGTGAAACCCTGTCTCTACTAAATGTACAAAAATTAGCTGGGCGTGGTGGCAAACGCCTGTAGTCACAGCTACTCAGGAGGCTGAGGCAAGAGAATCACTTGAACCTGGGAGGCAGAGGTTGCAGAGAGCTGAGATCGCGCCACTGTACTGCACTCCAGCCTGGTGACAGAGCGAGACTCCGTCTCAAAAAAAAATAAAACAAATATTCTATACATGGAATTAGAGAGCATCCAGACTGTTGCATGTATCAATACTGCAGGTTTTTTTTTTTTTACTTTTTGCATTTTTTGAAATGGAGTCTCACTCTGTTACCCAGGCTGGTCTTGAACTCCTGACCTCAAGCAACCCTCCTGCTTCAGGCTCCCAAAGTGCTGGGATTACAGGCATGAGCCACCTCATCTGGCCATAGCATATTATTTTTTATTTCTGGCAGAGTCAGGGCCTCCAGAGGACTCAACTGGTTCCTGTAGTGGCACTGGTTGCATTGTCCCCATGGCACAAAGACATGCTCTGTTGCAATAGACTAGGCTTCTCCTTATATGCCCTTGAGTGTATCCACTGGTGCAAGGCTTTTTCACCAAGCAAACAGACATTGAGTGCCTGCTGTATCCCAGGCACATGCTAGGTGCTGGGGGTGCAGCTGTGAACACACACCATGGTCCCTGACCTCCATGAATATTCTAGCCGAATTGGTGGGGAGTAAACAATAAACAGATAATCACAGAGACAGATACATAATGGCAAACTGTGATAAGTGCATGAAGCAAGCTGCTGGAGTACATAGCAGGGGCTTCCTTGTGCCAGGCAGGGGCTTGAAAACAAAGAGTTAGGAGGCAGCCCAGGGAAGGACAGCAGATGCTGCTTTTTGGAAATGTTCGTCCCCACTGAACCAACTTCTGAAAAACTATCCTAAGAAAATCGTCTTAGCCAGGTGTGGTGGCTCATGCCTGTAATCCCAGCACTTTGGGTGGCCAAGGCAGGAGGATCACCTGGGTTCACGAGTTCGAAACCAGCCTGGCCAACATGGCGAAACCCTATCTCTACTGAAAATACAAAAATTAGCCAGGTGTGGTGGTGGGCACCTGTAATCCCAGCTACTCAGGAGATTGAGGCAGGAGAATCACTTGAACCGAGGAGGCAGAGGTTTCAGTGAGCTGAGATCGTGCCACTGCACTCCAGCCTGGGTGACAGGGCGAGACTCCACCTGAAAAAGAGAAAAGAAAATCAAGAGTTAAGGGCATTCATTATGGCCTTATTTACAATAGCAGAATTTCAGTGTCCAGTCCTAGCTGAATGATGAGTTCAATAATGGTTCATCTATCAATGGAATGTTTTCAGCTATTAAAATGATGGCTTTGGCTACTGAATAGGTCTGCTAAAAAAAAAAAAAAAAAAGACTTCTACCTAGCTGTCTAGTTGGACACTGTGGCATGTGCCTGTAGTCCCAGCTACTCTGGAGCTGGGGTGGGAGGATCGCTTGAGGCCAGGAGTTCAAGGCTGCAGTGAGCTATGATTGTGTCACTGCACTCCAGCCTGGGTGACAAAACAAGACCATCGCTAAATAAATAAATTAACTTAAAAGATGGCTATGTAAAGTTGTAAGAATGATGTAACAGCATGGGGTAATACATATCTTATAATTTTTAAAAAAATTTTATTTGTGGAGACAGGGTCTCACTGTGTCACCCAGGCTGGAGTGCAGTGGCACAATCGTGGCTCACTGCAGCCTCAGCCTGCAGGGTTCAAGCGATCTTCCTGCCTCAGACCCCTCACTAGCTGGGACTACAGGCACACACCACCATGCCTGGTTACTTGTTTTTGTAGAGATGGGGTCTCATGATGTTGCCCAGGCTGGTCCCAAACTCCTGGGCTCAAGCGCTTGCCTCGGCCTCCCAAAATGCTGGGATTACAGGCATGCATCACTGTTCCTGTCTGTATCATATAATTTTAAATAATAAAAGCAGCCTCTACAACTAGGCAGCATGGTCTTAAGTCTATTTTTTAAACATAGAAAAAGAGCCAGGAAGGAAATGTAAACAATGTTAATAATGACTTTGATAGGGAGGTGGGTGGGATATGAAAGATTTTTTTTCTCCCTTTTGTCCTTGGAAGGAAATATCACTTTTCAGCAGTAGTTCTCTGTTGGGATGGTTCTAAAGTGGGGAAGATGAGACTTTTTCCTTTCACTTTGTACCTTTTCTGGTGCTCTGATTTAGAGCTCCTCAGTCTTGCCACTGTTGATATTTTGGGGTGACTAATTCTGTTGTGGGGGCTGTCCTGTGCACTGTAGGGTGTTTAGCAGTATCCCTGGCCTCTACCCACTGGATGCCAGAGGCACCCCCCACCCCAGCTGTGACAATCAGCAGTGTCTCCAGACAATATCCCCTAGTGGGGATCGGTGGGGGCAACATTGTCCCTGGCTCGGAACCACTGATCGAATTTATTATGACAACATATCCCTTTGCCACAAAAACAAATGATGGGCTAACCGTGTGTGTGCAG
Seq C2 exon
GTGAAGCCACTGCTGCAGGTGACACGGCAGGAGGAGGAGATGCAGGCCAAGGAGGATGAACTGCAGAAGACCAAGGAGCGGCAGCAGAAGGCAGAGAATGAGCTTAAGGAGCTGGAACAGAAGCACTCGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133392:ENST00000300036:20
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=0.773
Domain overlap (PFAM):

C1:
PF0061222=IQ=PD(14.3=8.1)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development