Special

HsaINT0107884 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 7B [Source:HGNC Symbol;Acc:HGNC:15906]
Coordinates
chr20:34987765-34988262:+
Coord C1 exon
chr20:34987765-34987914
Coord A exon
chr20:34987915-34988091
Coord C2 exon
chr20:34988092-34988262
Length
177 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGG
5' ss Score
8.41
3' ss Seq
CAGGCCCCTCCCTCTTGTAGTTC
3' ss Score
7.56
Exon sequences
Seq C1 exon
GTGGTGTTTGCTGTGGGGGCTCTGGCCAAGGCCACCTATGACCGGCTGTTCAGGTGGCTGGTGTCTCGGATCAACCAGACCCTGGACACAAAGCTGCCCCGGCAGTTCTTCATCGGGGTTCTGGACATCGCTGGGTTTGAGATCTTTGAG
Seq A exon
GTGAGGACAGGCCCTCACCTTGGCCTCTGTTCTCTCCAAGGTAGAGGACATGGGCCTGTGGGGGGGCAGAAGCCCTGGCCTTCTGCCTGGAAGTTGGGGGTGAACTCATGCCCCTCCCCGGGCCTCCCTTTCCCCATCTGCGAGAGGTCTGCTGAGCCAGGCCCCTCCCTCTTGTAG
Seq C2 exon
TTCAACAGCTTCGAACAGCTGTGCATCAACTTCACCAATGAGAAATTGCAGCAGTTCTTCAACCAGCACATGTTTGTGCTGGAGCAGGAGGAGTACAAGCGGGAGGGCATCGACTGGGTCTTCATCGACTTCGGCCTTGACCTGCAGCCTTGCATCGACCTCATCGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078814:ENST00000262873:16
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=FE(10.9=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(12.5=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:
CTATGACCGGCTGTTCAGGTG
R:
CGATGAAGACCCAGTCGATGC
Band lengths:
242-419
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