Special

HsaINT0107876 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]
Coordinates
chr20:34982459-34984715:+
Coord C1 exon
chr20:34982459-34982555
Coord A exon
chr20:34982556-34984691
Coord C2 exon
chr20:34984692-34984715
Length
2136 bp
Sequences
Splice sites
5' ss Seq
GCCGTAAGA
5' ss Score
5.75
3' ss Seq
TGTCTGTCTTCTTCCCCCAGCAA
3' ss Score
9.9
Exon sequences
Seq C1 exon
CGGAGAGTCGGGGGCCGGTAAGACGGTTAACACCAAGCGGGTCATTCAGTACTTTGCCATCGTCGCTGCCCTGGGAGACGGGCCGGGCAAGAAGGCC
Seq A exon
GTAAGACTTGCCCACTCGGGCATGCTCCCCGTTGCTTCTCGCTGTTTTTCTTTTCTTTCTTCCTCTCTTTTTTTTTTTTCCCCCTTTTTAAAAATTTTACTCCCCAGAACCCTGAGCCCTGCCTGAGCCTCCCACCCTGGTGGGGGACTCTGGCCTGAGCAAGGCTTGACCACAAAGGCTGTGGCCACCTGACGCGCCTGCCTTCGCCTTCCCATTGGTAAACATGGAGGGGTGGGGCCACGTTGCCGTTTCTAAATTTGTGTAATTTTTATCTTCCATTGTGACCTTCATATATTGAAAGAGTTTACTAGATGGGCTGCTTTTACTAAGCGTTGTTGTCTTGGTTTCCCTGACAGTTACCTGCTGCTGACACATTAGACACAGAGGTTGGCTGGCATGCAGGGCACTGGGCATTCCCAGCAGCCGGGGTTGGCAGGGCAATTTTGTGCCTTGTGATTTCTGTACAGTTTTTGGAAATTTCTGAAACAATGGGGCCAAGTTTTTTTGTTTTTGTTTTTAAGGCATAACATTTCATCCCTAGCCTTGGGGCCAGTTGTTCAGAGCCCTGTGGCTACCCCTAGATGGGCTGCCTTTTTCCAGAAGCCCGAGGCCTCCCTCCCCACCCAGTCCCTGCTCCTGGTCCTGTTAAGCCTTGCTTTATTCTGGGTGTTTTTCTTGTTTTTCCCCTGTTTTCTTTCTTTCTTTCTTTTCTCTTTCTTTTTTCTTTCTTTTCTTTTCTTTTCTTTTTTTTTTTTTTTTTTTGCCTTTTCCTTTTTACCCATTTGATTGTCTTGATTTTTGATTTTCATTTCAGTTTTGTTTTGTTTTGTTTTTGCTGTTGACTTTTTGGTCCTTTTTCCTCCTTCCCTTTCCTGCCCTGTCTTCCAAATCCCTAAAAAGGTCTCTGGGGACGTAACAGAAAGTTGGGTGGGTCAAGTGACAGGAAGAGATGTCAGGGAGAGGCCAGAGCTGGCAGGGACACAGCTGGAAGGGCAGAGGAGCACCTGGGCAGAAAGGAGCTGGGACAGTGGAGCCCAGGGGAGAGGGTCGGGCAAGGGAGGGGTGGGAGAGGCTGCCCGCAGGAGCCATGGCTGCAGGAACTTAAAAGATTGATCAGCTCCCCTTACCTTGGCCCCAAATTTGGCCAAACGGGCTAGAGAGAGCCCTGCACAAAAGCACTGGATGGGAGTGTATTGGGGGGTTCCACCTCCCCTGCCCAATGTCCCTGTGGGTATTTTAACTCTTGGGCTCCCTGGAGGTGAATGAATGACCACAAAGTCCGTGGTGGTATATCTGTTCCCTCCAGAATCCATTCCTTCCCTTCTCTCCCTTTCTTCCTTGGCTCCCAGCATCCGGAGTAGGGAAGAGAAGGAAAGGAAAAGGAAGGGAAAGTGAGGATGAGGCTAGGATGGGGAGAAGGAGGATCTGCTCAATTCACTTAGTCCCCCTGGGTGACACACAGGACCGCTGTGGCGTCCAGGCGGCAGGATGCTGGGCACCTGCCCTGCCGCTCCTGACTTGCTGTGTGGCCTTGAGCAGATCCACTCCCTGCCCAGAGCTAAGTCTCCTCATTTGCAAATTAGGGCTAATAATGGGCACCTGGCAGGGCCTTTGTGCGCACTGGTAGGTATACAGGCAGACAAACAATGAAGACACACCCAGTTGCATTACAAAGGAGAGGTGTGTAAGGTCATAGTGGGAGGTTAGGGCAGGAAGGTTCAGACCAGGAAGAGGTCTATTCCAGCTTTGGAGCAGCCAGGAGGCCTTCCTAGAGGAGGGGGCACTTGGGCTGGGCTCTGGAGGGCCCTAGATTTTAGTCGGGAGGCCCCTGGGGCTTGGAGCAGGGCCACTGCATGGAGACTAGAAAATGAAGGGAGGCCAGAGGCCGGGCTGGGGCAGAGGAGGCTGCAGGTGGAGACTCTGGCTGGGGCTGTGCCACTCCCACTTTCCAGCATTTTGCCTCCTAACAGCTGCAGGAGGGTCAGGCCGAGGGGCTGAGGGTGGGGGCCATGCATTCCGGTGACTAACTCCACCCCCCTGTCCTGCTGCCCGCTGCCTCCCGCTGATACCCTGCCCCACCCCGCCCTTCCCCACCGGAGGCCTGGCCCTCTAATGTTGTCTGTCTTCTTCCCCCAG
Seq C2 exon
CAATTTCTGGCAACAAAGACGGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078814:ENST00000262873:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.121 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(4.7=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(1.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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