Special

HsaINT0108916 @ hg38

Intron Retention

Gene
Description
myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]
Coordinates
chr11:77204076-77205617:+
Coord C1 exon
chr11:77204076-77204229
Coord A exon
chr11:77204230-77205461
Coord C2 exon
chr11:77205462-77205617
Length
1232 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
GCCCACGCCTCCTCCTGCAGGTA
3' ss Score
10.17
Exon sequences
Seq C1 exon
CTGTGCTCAAGTACATGGGCGACTACCCGTCCAAGAGGACACGCTCCGTCAACGAGCTCACCGACCAGATCTTTGAGGGTCCCCTGAAAGCCGAGCCCCTGAAGGACGAGGCATATGTGCAGATCCTGAAGCAGCTGACCGACAACCACATCAG
Seq A exon
GTGAGCCAGGCACAGTGGGCGGATGAGGGGCAGACCTCACCTGCTGTGACGGGCAGCTCTTACCCTCCTGAGGCAGCTGCTGGCTCTGCCTGGATGCAGTCCTTCCTCACACAGAGCCGGGAGCTGCTCATGGGCCCCCTCACATCCTAGCTTGGCCCCAACGCCCAAGGAGGGCCTAGCAGGAACTGGGAGGTGGTGGATGTCTTCCTTTGAGTCTGTCCTCTAAGGGTAACAGCCCCAGCTCCTCCTAACGTTTGGCTGGAGCCTCGTCTGGATGCCCCTTCCCTGCCTAGACCCTGCTGTCTGCCTGCAGGTCCAGCTCAGTCAAGTGTCCCCTCCCTGGTGCAGGCTGGGCCGGCTGTCAGCTGGAAGCACTGGCTGAAAACTCTCATGGGTTTGAGTGTTGGTCCCAATGCCCAAAGGGTGCCACCTTCTCCTCCCGCTGGGACAGCCCAAGACAGGAGTAGAAAGTCAGGCACAGGCTCCTCTCAGAGTCTGAGAGAAGCTCCACCCTCTCTCCTTACACCCAGCCCCCCGCCTTCCTCCCCAGCTGTGTCACCCTCTACATCTCTTCCACAAATCCATCCTCAAACTACACATCAGCTCTTTTGACAGTGCCAAACCTTTGTACATACTGTGCCCACAGCCAGGAAAACTTTTCAGCCCCTTCTCTGCATGCCGTAATTTGCTTCATCCTTCAAAGCCTAGTTCAAATGCCACCTCCTCCTAGAAGCCCTCCAAACTTCCCACTGTCAGGCCCAAGAAGCTCAGAGTGGTGGCTGAAGGAGCCTGGGGTGGGACTGGTCTAACTCGTTGCCACTCAAAGTAGAGGTGAATTAAAGAGCTTCTGCGAAAATATAAATCACACTGCTTCCTTCATGGAGAAAGTCTTGCTATGGAAACAAACAAAAAGCCTCAGCTGAAGCAGAGTGCATGGTAACCCGGTGGCTTTTCATTGTGGCATAAGCCCCTTATCTCCACGTGGACTGGTAGCAGTGTGTGGCCTGGCGCGGTGGGCCAGGCACACTTTGGGTAGCACTAGTTGCATCTGGCTGTCAGGGAGAGGGGTCTGTAGGTAGGGTGAGGGGTCCTGAGATAGGGTAAAGGTCAGGAGGGACGGTGCTGCTGTGATGAGCAGCTGAGGGGTACATGGCCCCCTCACCCGGGGGTGCACAGGTCCTGTGACTCCCGATGGCAGCTGCCCCTGCTGGAGCCCACGCCTCCTCCTGCAG
Seq C2 exon
GTACAGCGAGGAGCGGGGTTGGGAGCTGCTCTGGCTGTGCACGGGCCTTTTCCCACCCAGCAACATCCTCCTGCCCCACGTGCAGCGCTTCCTGCAGTCCCGAAAGCACTGCCCACTCGCCATCGACTGCCTGCAACGGCTCCAGAAAGCCCTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137474:ENST00000409709:39
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=0.000
Domain overlap (PFAM):

C1:
PF0078412=MyTH4=PU(34.6=71.2)
A:
NA
C2:
PF0078412=MyTH4=FE(48.6=100)


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:
GCTCAAGTACATGGGCGACTAC
R:
CTCAGGGCTTTCTGGAGC
Band lengths:
306-1538
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