Special

HsaINT0108939 @ hg38

Intron Retention

Gene
Description
myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]
Coordinates
chr11:77181380-77182154:+
Coord C1 exon
chr11:77181380-77181589
Coord A exon
chr11:77181590-77181950
Coord C2 exon
chr11:77181951-77182154
Length
361 bp
Sequences
Splice sites
5' ss Seq
GAGGTACCA
5' ss Score
6.43
3' ss Seq
ATACCTCTTGTCTCCTTCAGGAC
3' ss Score
11.62
Exon sequences
Seq C1 exon
GAGCGCCTGGCCCAGCTGGCTCGTGAGGACGCTGAGCGGGAGCTGAAGGAGAAGGAGGCCGCTCGGCGGAAGAAGGAGCTCCTGGAGCAGATGGAAAGGGCCCGCCATGAGCCTGTCAATCACTCAGACATGGTGGACAAGATGTTTGGCTTCCTGGGGACTTCAGGTGGCCTGCCAGGCCAGGAGGGCCAGGCACCTAGTGGCTTTGAG
Seq A exon
GTACCAGGCTAGGGACAGGGGCTCCAGAGGCCCACACACACCGCTTGTGTTGATCCTCCCTCCTTCTGTGCCCTTGGCCTTAAAGCCCACCCAGTCCCTCTGAACAGTGGGGAGCAGAGATGAACTGGGTCCGGGCTGCAGGTCCCAGGTCCTGTCCCTCTCCAACGCCCTTCTCAAGTTTTTTTTTTTGTTTTTTTTTTTTTTTTTTTTTTTGAGATGGGGTCGTACCCTGTTGCTCAGGCTGGAGTGCAGTAGCGTGATCACAGCTCACTGCAGCCTTGAACTTCTGGGCTCAGGCGATCCTCCCACCTGAGCTTCCTGAGTAGCTGGGACTCCAGGGCATACCTCTTGTCTCCTTCAG
Seq C2 exon
GACCTGGAGCGAGGGCGGAGGGAGATGGTGGAGGAGGACCTGGATGCAGCCCTGCCCCTGCCTGACGAGGATGAGGAGGACCTCTCTGAGTATAAATTTGCCAAGTTCGCGGCCACCTACTTCCAGGGGACAACCACGCACTCCTACACCCGGCGGCCACTCAAACAGCCACTGCTCTACCATGACGACGAGGGTGACCAGCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137474:ENST00000409709:23
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.773 A=NA C2=0.485
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAAGGAGAAGGAGGCCGCTC
R:
TCGTCGTCATGGTAGAGCAGT
Band lengths:
357-718
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