Special

HsaINT0108982 @ hg38

Intron Retention

Gene
Description
myosin VIIB [Source:HGNC Symbol;Acc:HGNC:7607]
Coordinates
chr2:127565233-127566827:+
Coord C1 exon
chr2:127565233-127565385
Coord A exon
chr2:127565386-127566642
Coord C2 exon
chr2:127566643-127566827
Length
1257 bp
Sequences
Splice sites
5' ss Seq
TATGTGAGT
5' ss Score
5.56
3' ss Seq
ACCACCTGCTTCCTTCCCAGACA
3' ss Score
9.55
Exon sequences
Seq C1 exon
GAACACTGGATCCGAGCAGAGGACTTTGGTGTCCTCAGTCCCATGCACCCCAACTCAGTCCAGGGTGTGGACGACATGATCCGCCTGGGGGACCTGAACGAGGCAGGCATGGTGCACAACCTCCTGATCCGCTACCAGCAGCACAAGATCTAT
Seq A exon
GTGAGTCTCCCCAGCCCTGTGTCCACAGGGGAGCCCCTCACAGGTGCCAACCTCCTGGACAGGGAGAAGAAAATGATGCACAGGGGGCACTGCCCCCCATGCCCTCACTGAGGGAGGTGGGCGAGGTGCCTAACTTTTCCCAATCTCTGCTGCCCAGTCCCAAACAAGGAGGGTGATCCCACCCTGGAGGGGAGGAAGCCAATGCGTAGAGTGACAGCACAGTGCCTGGCACAGTCTCTGCTCAGTGAGGGCTGCAGATGGCCATCAGGTGGCCATCATCCTCTGCCCTCTCCTTCCCAGGCATGTTGTAGAGACAGAGTCACTAGACAGAAAGCCCCTGGCCTCCCAAGAGTGAGGCCCGTGACAGCCCAGATCCCAAGGTCCTGATTCACCAGACGAGGGGGCCATGGGGATGGATGTGGGCCCTCCGTGCAAACCTGGCCTGGATGGAGGTTCACTCCAGCCTGAAGCTCTCATCCTGGTTCCAATGCAGATTTTTCCAGGGGAGGTGGTATTCCAAAACCGACACCAGTTCGGCCTAAGTAGGTGTGGCCTGCAGAAGCCACTGCCTGCCTGGGCCTCTCTGGTCTGGAGGGGTGGCTAGCTTGGTTCTGACTGGCCCTTCTGGGCTGCTCAGAGGAAAGCAGCTTGTGCTTCCAAAGGGCTTTTGCCTGCACTCCTCATCTGGTGGCACAGCCTGAAGCCAGAGGGCACGTCCTCTCCTTTCCTAAAGTGAAAACCAGGACACCATGGTCATGTGGCTTATTGTGCAGGCTCTGCCTGCCGCACCCCCTGAGGGGCAGTGGGGCTGGGTGGGGGCTCCAGATGGGCAGCTGATCCAGGGCGGAGGTCCCAGGGGCACACAGAATTTGGGGTTGGGGTCCGTGAGGCCCAGTTGTTGACCAGCCTATATGAAAGCCCCTGCGGGATGCAGGTGAAAACCCATTTCATACTTAGTCCATTTTTATCGAGCCCCTTCTAAATACCAGGCAGGGTACAAAACAGTTAACATTTGATCTTCCTGGAAATATGTTCCCTGGGAGCTCACCTTCCTGGTGGATATCCCATCTTCCCAGAGGAGAGATCTGCGCAGCTGAATGTCTGATCTCCCTGGCCCAGAATCAGATTCTACTTCCCCACCAAAGTCAGTGGCCCTGATAACCCCGAGGGCAGAGCCAGAGCCAAGGCCAAGGCCAAGGCCAGGGCCGAGTACCTCTGCCAGGGGCAGAGGGCACTGACCACCTGCTTCCTTCCCAG
Seq C2 exon
ACATACACAGGCTCCATCCTGGTGGCCGTCAACCCGTTCCAGGTGCTGCCGCTCTACACCCTGGAGCAGGTACAGCTCTACTACAGCCGCCATATGGGCGAGCTGCCCCCGCATGTCTTTGCCATCGCCAACAACTGCTACTTCAGCATGAAGAGGAACAAGAGGGACCAGTGCTGCATCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000169994:ENST00000409816:3
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:
PF0006316=Myosin_head=PU(4.1=54.9)
A:
NA
C2:
PF0006316=Myosin_head=FE(8.9=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:
GAACACTGGATCCGAGCAGAG
R:
CTGATGATGCAGCACTGGTCC
Band lengths:
338-1595
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