HsaINT0107834 @ hg38
Intron Retention
Gene
ENSG00000197616 | MYH6
Description
myosin heavy chain 6 [Source:HGNC Symbol;Acc:HGNC:7576]
Coordinates
chr14:23403715-23404388:-
Coord C1 exon
chr14:23404296-23404388
Coord A exon
chr14:23403779-23404295
Coord C2 exon
chr14:23403715-23403778
Length
517 bp
Sequences
Splice sites
5' ss Seq
TTTGTGAGT
5' ss Score
5.91
3' ss Seq
TCTGTCCCATTCGTCCCCAGGGG
3' ss Score
12.07
Exon sequences
Seq C1 exon
GGCACCCTGGAGGACCAGATCATCCAGGCCAACCCCGCTCTGGAGGCCTTCGGCAATGCCAAGACTGTCCGGAACGACAACTCCTCCCGCTTT
Seq A exon
GTGAGTGCCTTTGACCACTCCCAGTGGCCTCATCCAGCCTTGACAAGAAAAAGGGGGTGCTGTTTTGCCACACCCAGTTGATTGTACTGTATCTGGCTTTGGGATATCAACATGCACACGTTGGTGGGAAGAGAGCATAGGCTTTGGAGCCAAAGGTCTGACTTTCCACTTGCTCAGCAAGTCCTTACACCTCTCTGAGCCCTAGTTCCTTCACCTGTGAAACAGGGGGACTAATATCCACCCTGCAGATTACTGGGAGGATTAGGTGAGATCATATGAGAGGTATGAGCAGGAGGCATTCTGTATGTGTTCCCCTCTGGGCCGAGGTTCCACTAGGAGGTCCCTGCACAGTGTGTGAGGGTGGCATCCTCTGCCCGGCTTCACTTATACTCAACTGAGACACCAAAGAGGTCGTTTACATTTCCAGAACCATCCAGGGCTTCTGGGCTGAACAGAGGGCCAGGATTTCACTCTGTCCTTCCCGCCAGTTCCCTCACTCTGTCCCATTCGTCCCCAG
Seq C2 exon
GGGAAATTCATTAGGATCCACTTTGGGGCCACTGGAAAGCTGGCTTCTGCAGACATAGAGACCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197616:ENST00000356287:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.032 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0006316=Myosin_head=FE(4.4=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(3.1=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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