Special

HsaINT0108908 @ hg38

Intron Retention

Gene
Description
myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]
Coordinates
chr11:77190697-77192278:+
Coord C1 exon
chr11:77190697-77190870
Coord A exon
chr11:77190871-77192050
Coord C2 exon
chr11:77192051-77192278
Length
1180 bp
Sequences
Splice sites
5' ss Seq
AAGGTATGG
5' ss Score
9.26
3' ss Seq
CCTCCCCTCTGTGCCCACAGGTG
3' ss Score
13.59
Exon sequences
Seq C1 exon
GCCACCAAGTCCAAGAAGCCAATCATGTTGCCCGTGACATTCATGGATGGGACCACCAAGACCCTGCTGACGGACTCGGCAACCACGGCCAAGGAGCTCTGCAACGCGCTGGCCGACAAGATCTCTCTCAAGGACCGGTTCGGGTTCTCCCTCTACATTGCCCTGTTTGACAAG
Seq A exon
GTATGGCCGCCCGGAAGCACCTCCTCCCGGAAGCACCTCCTCCCGGCCCCACTCCGGGCTGCCAGTGCTGCCACCTACTTGCCGGGGCTATTCACCCTTGAGCACCTCGGTTTCCCCCTGAGCCTGTGCTAATTGGCTCTGCCTGACTCCTCAGGACTGCCGAGAACTCGGCCAGGTGCGGTGGTTCACACCTGTAATCCCAGCACTTTGGGAGGCTGAGGCGGGCAGATCACAAAGTCAGGAGTTCGAGACCAGCCTGGCTAATGTAGTGAAACCTCGTCTCTACTAAAAATACAAAAATTAGTGGAGCACGGTGGCGCACGCCTGTAGTCCCAGCTACTCGGGAGGCTGAGGTAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGTGGTGAGCTGAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCATCTCAAAAAAACAAACAAACAAAAAACTGCTGAGTGCTCTTCAGCACCTGAGGGAAAACCCAGCAGTAGGATGTCCTCAGTCCTGTGTCCTCAGGCCCAGTGAATCCTCTCCTGGTGCTGAAGGAAGAGCATGGCACAGGCTGATGGGAGGGCTGCGCAGCCCTTGTGTGCAGATGGGAATGGAATTCCCTCTCAGGTTGCCACGGCATCTGATGGAGAAACTCCTCAGCAAACAGGAGTTCCTTCACACTTGCCCTGAAGCAGCTGGAGTGTGGGCGTCCCGCAGACTCACCTCGGAGGCTGGAGCCTCCTCGGCTGAGCGGGACCTGGGGCTTGGGTGATTTTGCCTCCACCCCCAGCAACGTCATGCTCAGCAGAGGGGCCCCCGCCCACAAGCCCAGGGGAGGTACCGTGTTGCTGGACACAGTTTGCCTGGATTTTTCTCACCGATGCTCTTATGTTTCCAGGTACTGTCTGTTCAGTTTCCCAAAAAGCTTCCACTAGAAAATGGGAATTCCCACGTCACCGTGCCCAGAACTGAGGCTAGGAAGGCAATGGTGGGGGTGCGGCTTAGAGCCCAGGGCTAGAATCTGGTCTGCCTCCTGGGGGCCTTGGACGTGTCCCTGCCCCTCGCTGGGCCTCCGTTTTCTGTCTGAACTGACCGTTGGCCCCGTTGAGGCTCCTCATAGTCCTTCCCTGACTCTGTGCCTGCTCCCCTCCCCTCTGTGCCCACAG
Seq C2 exon
GTGTCCTCCCTGGGCAGCGGCAGTGACCACGTCATGGACGCCATCTCCCAGTGCGAGCAGTACGCCAAGGAGCAGGGCGCCCAGGAGCGCAACGCCCCCTGGAGGCTCTTCTTCCGCAAAGAGGTCTTCACGCCCTGGCACAGCCCCTCCGAGGACAACGTGGCCACCAACCTCATCTACCAGCAGGTGGTGCGAGGAGTCAAGTTTGGGGAGTACAGGTGTGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137474:ENST00000409709:30
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.013
Domain overlap (PFAM):

C1:
PF0078412=MyTH4=PD(1.9=3.4),PF093795=FERM_N=PU(50.5=79.3)
A:
NA
C2:
PF093795=FERM_N=PD(47.3=56.6)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCACCAAGTCCAAGAAGCCAA
R:
GTAGATGAGGTTGGTGGCCAC
Band lengths:
353-1533
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