HsaINT0108650 @ hg38
Intron Retention
Gene
ENSG00000136286 | MYO1G
Description
myosin IG [Source:HGNC Symbol;Acc:HGNC:13880]
Coordinates
chr7:44970040-44970737:-
Coord C1 exon
chr7:44970592-44970737
Coord A exon
chr7:44970155-44970591
Coord C2 exon
chr7:44970040-44970154
Length
437 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
3' ss Seq
AAGGCCCACCCCACCCCCAGTTT
3' ss Score
4.14
Exon sequences
Seq C1 exon
GCAGTGTACCAGCGGCTGTTTGAGTGGGTGGTGAACAGGATCAACAGTGTCATGGAACCCCGGGGCCGGGATCCTCGGCGTGATGGCAAGGACACAGTCATTGGCGTGCTGGACATCTATGGCTTCGAGGTGTTTCCCGTCAACAG
Seq A exon
GTGGGTGGCTGGCCAGCCACATCTCCACCTCTGACACCCAGCAGCTTTGCCCACTTAGTTCTGGAAAGCTCGGCTGGGGCTGGGCAGCAGGAATGTTGGGGTTTCTCCCGGCTGGTCCCTGGGCCCAAGGCTCATGCCTCCCAAACCTGCCTCACCTGCACCCTCTGACCATTGATGTCCTGATGGAAGGCAGAATTACGGGGCATGAGTAATTCCTGGTTGTGACTCCCAAGTCCACTCCAGAACGTGCATGCAGGAGGTGTGGGTGGGGTAAAGGAGTCCAGGGCAGGGATGCATAAGCCACAGGGAAGCCACACAGGGTGCTGGCACCAGAACCCTCAATGAACATTAGCAGAGATGTTCAGGGGAGCAGCCACCCATTACCATGCACTCCACAAGCAGCGACCTCCCCTCTGAAAGGCCCACCCCACCCCCAG
Seq C2 exon
TTTCGAGCAGTTCTGCATCAACTACTGCAACGAGAAGCTGCAGCAGCTATTCATCCAGCTCATCCTGAAGCAGGAACAGGAAGAGTACGAGCGCGAGGGCATCACCTGGCAGAGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136286:ENST00000258787:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.122 A=NA C2=0.000
Domain overlap (PFAM):
C1:
PF0006316=Myosin_head=FE(7.0=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(5.6=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
GTACCAGCGGCTGTTTGAGTG
R:
CTCTGCCAGGTGATGCCCTC
Band lengths:
255-692
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