Special

HsaINT0107833 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:7576]
Coordinates
chr14:23404296-23404822:-
Coord C1 exon
chr14:23404711-23404822
Coord A exon
chr14:23404389-23404710
Coord C2 exon
chr14:23404296-23404388
Length
322 bp
Sequences
Splice sites
5' ss Seq
AAGGTGCCA
5' ss Score
3.41
3' ss Seq
CAGTTCTGCTCCTTTCATAGGGC
3' ss Score
7.69
Exon sequences
Seq C1 exon
GGGAGAATCCGGGGCGGGGAAGACTGTGAACACCAAGCGTGTCATCCAGTACTTTGCCAGCATTGCAGCCATAGGTGACCGTGGCAAGAAGGACAATGCCAATGCGAACAAG
Seq A exon
GTGCCATGGGGGACACAGGCTCGGCAGAACAGGGGTTGGGGGGCAGGCTGACCCGAGTTACCCCTAACCCTCCCCTCCCTGTGACGTGGTGGGGACAGCCACACTGAGCTGGGCTCCCGATGGTCAGCCCAGTATGGAAGACCTTCCTGACAGGAGACACTCACCCTGAGGTCTGGGTAGGATCCTGTGGAGTCGCAGACCCACTAGCGGTTCACCCAGCCCCGCACCCCCATTCCTCAGGGCCAGGGCAGCCTCCCTGCCCTCTCACCACTGCCTGGAGGTGGATGGAGGATGAACCCATGCAGTTCTGCTCCTTTCATAG
Seq C2 exon
GGCACCCTGGAGGACCAGATCATCCAGGCCAACCCCGCTCTGGAGGCCTTCGGCAATGCCAAGACTGTCCGGAACGACAACTCCTCCCGCTTT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197616:ENST00000356287:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.132 A=NA C2=0.032
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(5.4=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.4=100)


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:
GGGGAAGACTGTGAACACCAA
R:
AAAGCGGGAGGAGTTGTCGTT
Band lengths:
190-512
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