Special

HsaINT0108917 @ hg19

Intron Retention

Gene
Description
myosin VIIA [Source:HGNC Symbol;Acc:7606]
Coordinates
chr11:76916507-76917247:+
Coord C1 exon
chr11:76916507-76916662
Coord A exon
chr11:76916663-76917141
Coord C2 exon
chr11:76917142-76917247
Length
479 bp
Sequences
Splice sites
5' ss Seq
GAGGTACAG
5' ss Score
6.62
3' ss Seq
TGCCCCTGCTGCCTTTTCAGAAA
3' ss Score
10.01
Exon sequences
Seq C1 exon
GTACAGCGAGGAGCGGGGTTGGGAGCTGCTCTGGCTGTGCACGGGCCTTTTCCCACCCAGCAACATCCTCCTGCCCCACGTGCAGCGCTTCCTGCAGTCCCGAAAGCACTGCCCACTCGCCATCGACTGCCTGCAACGGCTCCAGAAAGCCCTGAG
Seq A exon
GTACAGCGGCCACCAGGGGCAGGGACAGACACTGGGGCGGGCTCCTGGCCACGCGGGGCTTGTGGGATGAGCCCCTTGGGGATGAGGACCACATAGCAGTTGGGCCCACCCCTGGGGTACCTCAACTGCCAGCTAGACGGAGGTGCGGATCCTGCAGCTGCTCAGGATGCAGCTGGAGAGTCCGGCTGCTCGGGAGTGCTCAGCCCAGAGCTCCCAGGCTATCGGGTGGGCACAGACACCTGGGCCCACTTCATACTCTCCGAGGGCACTTGTGTTCTTCACTTTGCTGGGCCTCTCCACACCCATCGTCCCATTTTACAGATGAGGAGCTCAAGGCTCTGGGAGACTCAGTGGCCGGTCACATCATAGGAAGTGGCAGGCGGGGATCAGAACTGGGGTTGTCTGCCTCCAAGTGTCCCGGTCCCCTGGTCTCCACAGTCCCACGCACATGCCCCCTGCTGCCCCTGCTGCCTTTTCAG
Seq C2 exon
AAACGGGTCCCGGAAGTACCCTCCGCACCTGGTGGAGGTGGAGGCCATCCAGCACAAGACCACCCAGATTTTCCACAAAGTCTACTTCCCTGATGACACTGACGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137474-MYO7A:NM_000260:40
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0078412=MyTH4=FE(48.6=100)
A:
NA
C2:
PF0078412=MyTH4=PD(15.9=47.2),PF093795=FERM_N=PU(8.5=22.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAGGAGCGGGGTTGGGAG
R:
TCGTCAGTGTCATCAGGGAAGT
Band lengths:
254-733
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