HsaINT0107889 @ hg38
Intron Retention
Gene
ENSG00000078814 | MYH7B
Description
myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]
Coordinates
chr20:34990234-34990825:+
Coord C1 exon
chr20:34990234-34990310
Coord A exon
chr20:34990311-34990737
Coord C2 exon
chr20:34990738-34990825
Length
427 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
TCACTCTTCCCCACTGCCAGGAG
3' ss Score
7.35
Exon sequences
Seq C1 exon
CTGAGCCCCCCAAGTCTGGGGTGAAAGAGAAGCGTAAGAAGGCAGCATCGTTCCAGACGGTGTCCCAGCTGCACAAG
Seq A exon
GTAAGGCCCCATCTGGGAGACAGACCCTCCCTCTTGGCAGCCTCCAGCCCCGTCCTTCACCCCCTGCCCTGTCCCCTGTGCCTTGGGCGGGCGGCTGTTAAGACTTGCAGTGATGTTTAACTCCTCTCCACGTGAACATCACAGCAAGTCTGTGCTGCTTCCCGTCCCTACGCTGCCTGGGCAGGGTTTGTGGGGAAGGGGTGGGAGCCCTGGGGCTCTGGGAGGGACGGGGATTTGGCAGGGAAGTGAAGACTTTGGTGGTGGTGATGGGAGACAGCGAAGGGTCTCCCATCACCAGAATGAGAGTGAAAGAGCAAAAGTGCAGGGCACTTAGGGCCCTGCTCCCGTCTCGGTCCTGACCACTGCGGCATCCAATTCTGGTTCTCTGCCCCCTTTGTGCCTTTCCCTCACTCTTCCCCACTGCCAG
Seq C2 exon
GAGAACCTCAACAAGCTGATGACCAACCTGCGGGCCACACAGCCCCACTTCGTCCGCTGCATTGTCCCCAACGAGAACAAAACCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078814:ENST00000262873:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.462 A=NA C2=0.033
Domain overlap (PFAM):
C1:
PF0006316=Myosin_head=FE(3.6=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.2=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Cow
(bosTau6)
No conservation detected
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
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
- Pre-implantation embryo development