HsaINT0107907 @ hg38
Intron Retention
Gene
ENSG00000078814 | MYH7B
Description
myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]
Coordinates
chr20:35000293-35000893:+
Coord C1 exon
chr20:35000293-35000689
Coord A exon
chr20:35000690-35000767
Coord C2 exon
chr20:35000768-35000893
Length
78 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGG
5' ss Score
6.92
3' ss Seq
GAGACTCCTCTTCCCCTCAGAAC
3' ss Score
7.83
Exon sequences
Seq C1 exon
GCGCAACCACCAGCGAGCTGTGGAGTCCCTGCAGGCCTCCCTGGATGCAGAGACACGGGCCCGCAATGAGGCGCTGCGGCTCAAGAAGAAGATGGAGGGTGACCTCAACGACCTGGAGCTGCAGCTGGGCCATGCCACCCGTCAGGCCACAGAGGCCCAGGCTGCCACGCGGCTGATGCAGGCACAGCTCAAGGAGGAGCAGGCAGGGCGGGACGAGGAGCAGCGGCTGGCAGCTGAGCTCCACGAGCAGGCGCAGGCTCTGGAGCGCCGGGCCTCGCTGCTGGCTGCGGAGCTGGAGGAGCTGCGGGCTGCCCTGGAGCAGGGCGAGCGCAGCCGGCGACTGGCAGAGCAGGAGCTTTTGGAGGCCACCGAGCGCCTCAACCTTCTGCATTCGCAG
Seq A exon
GTGGGGACAGGAGTCCCTGGGGACAGAGCAGGTGCAGGCCTGCTGGCTGGCTGGCTCTGAGACTCCTCTTCCCCTCAG
Seq C2 exon
AACACAGGCCTCCTAAACCAGAAGAAGAAGCTGGAGGCGGACTTGGCCCAGCTGAGCGGGGAGGTGGAGGAGGCTGCACAGGAGAGGCGGGAGGCTGAGGAGAAGGCCAAAAAGGCCATCACTGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078814:ENST00000262873:37
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.729 A=NA C2=0.905
Domain overlap (PFAM):
C1:
PF0157614=Myosin_tail_1=FE(15.4=100)
A:
NA
C2:
PF0157614=Myosin_tail_1=FE(4.8=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:
GACTGGCAGAGCAGGAGC
R:
TTTTTGGCCTTCTCCTCAGCC
Band lengths:
172-250
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
- Pre-implantation embryo development