Special

HsaINT0108824 @ hg19

Intron Retention

Gene
Description
myosin VB [Source:HGNC Symbol;Acc:7603]
Coordinates
chr18:47361714-47363255:-
Coord C1 exon
chr18:47363081-47363255
Coord A exon
chr18:47361795-47363080
Coord C2 exon
chr18:47361714-47361794
Length
1286 bp
Sequences
Splice sites
5' ss Seq
CAGGTACAG
5' ss Score
8.68
3' ss Seq
TCCGTTTTTATCCCCAACAGATT
3' ss Score
9.64
Exon sequences
Seq C1 exon
GTACAATATAAGTCAGCTTGAGGAGTGGCTTCGGGGAAGAAACCTTCACCAGAGTGGAGCAGTTCAGACCATGGAACCTCTGATCCAAGCAGCCCAGCTCCTGCAATTAAAGAAGAAAACCCAGGAGGACGCAGAGGCTATCTGCTCCCTGTGTACCTCCCTCAGCACCCAGCAG
Seq A exon
GTACAGTCACTTTGCACCTCTGTCAACATGGTATTCCAAGGAAGCCCTGAGTCCATTCCAAGTCTGTTCTCGTTGGTGGTTATTTGTTAGTGTTGCACTCCCACCCTTTATATACCCCTAATGAGACAATTTTGAAGTGCAGCTGATGGGATATTCCTAGATGAACCAAAAACCATTTGGTCTGTGAAACAAGATGCCACAGATACTGTTTTCTAGTAACTCTCTATCCCTCTTACTCACTTAAAAAGATAAGGTAGCAAACTCACAAAACGTTAAGTTTAGGTAAAAACTTCTTTAAATATAATGAATTCTGGAATGTTTCTTACATAGAAATCCACAAATTTTCAGAAATTGGCAGCATCAGGTATTTGCTTTCTTTACAAATATAACTGTAAGAAAAACCTTTTCTTTAAAACTAATTGCAATATGGTCATATTTTCACTCACACTCATTTATATTGTTTTAAATGAAGTCATTAAGAACTTAGGGGCATTTAAGTGTTACTTTCCTTTTCCCTAAAAAATGTATAACCATGATTCAGTTGCCGACACATTGCCAGTCCCTGAAAGATAAATAACAAAATCCAAACTCAGTACAGAAAAACACATCTTAATATAGCAAAGTGAACACCTTTCCTTACCTCCTCTGCTTACTATTAAAATATTAAATATCTAACTCTTTAAAAAACTGCTTCCTTCTGTAAACATTTCCAGAAAGTCTTCAAACATTTTTCTTCTCTTTAAATACATTTCACTTAAAGTAAGTTTCCTTCTAGATGCAGCTGGCATTGCATTTGGGCAGTCTACTTCCACCAAACCAGTGGTAGGCAGACAAAAGAGTATCTCCTGTTCAAATACTCATTTGTAAACAATGTTGGGGGACAGGGGGTAGTTAGGTATTAAACAAGACCTTTCTCATCTAAGGTAAGATCTCCAGTACTCTTCAGAAGAAACCTTTAAATTACTAGTAGATATGAGGCTGAGGATTTCAGGCAACTGCATTCTAAACTCCTCATTGTGTATACCAATGAGCATAGTGGGGAGGGGCAGGTGGGTTTACAGGAGACATGAGTTCGGTGAGAGGGCTCAGATCCACCTGACAAAGCTGTGGGCTCTAGTTTCCTGGATGCAGGCTCCAAGTGTAAATGTCAGTCCAGCTCCATCTGTGTTGTGGGCCTTGTCTAAAGAGGATCATACTCTTGTACCAATGTCACATATTCTTTAAAGTTCAAAAGTTGTCTCATGTTCATTTAGCTCTGTGCTAAATTCCGTTTTTATCCCCAACAG
Seq C2 exon
ATTGTCAAAATTTTAAACCTTTATACTCCCCTGAATGAATTTGAAGAACGGGTAACAGTGGCCTTTATACGAACAATCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167306-MYO5B:NM_001080467:38
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:
PF0184314=DIL=FE(54.7=100)
A:
NA
C2:
PF0184314=DIL=PD(12.3=48.1)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
ACAATATAAGTCAGCTTGAGGAGTGG
R:
CTGGATTGTTCGTATAAAGGCCAC
Band lengths:
254-1540
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