Special

HsaINT0108782 @ hg19

Intron Retention

Gene
Description
myosin VA (heavy chain 12, myoxin) [Source:HGNC Symbol;Acc:7602]
Coordinates
chr15:52611257-52613706:-
Coord C1 exon
chr15:52613556-52613706
Coord A exon
chr15:52611540-52613555
Coord C2 exon
chr15:52611257-52611539
Length
2016 bp
Sequences
Splice sites
5' ss Seq
TTGGTAAGG
5' ss Score
8.92
3' ss Seq
CAATTGAAATACTCCTGCAGTCT
3' ss Score
2.96
Exon sequences
Seq C1 exon
GGCTTTATGAAGCACAACACATCTCGCCAGAATGAACACTGCCTCACCAATTTTGACCTGGCTGAGTATCGGCAGGTGCTGAGTGACTTGGCCATTCAGATCTACCAGCAGCTCGTGCGGGTGTTAGAGAACATCCTTCAGCCAATGATTG
Seq A exon
GTAAGGCCAGGGCCCCACTGGGCATTGCAGCCTGCCTATCATTCATGCCCATCGATAAGTAGCCACCAGTGGCACATGTTTCAGGGCAGGTATTCATTTGGGGAGCATAAAGTAGTAAGATACAGGGCTAAAATTAGCCGAGGAATCCCAGAAACCCAGCCATAGTTAACTGGGATACATCGAAATCACTGTTTCCACAAGACTGAAACAGTAGTATATGGTTTCCTTCCCTAATGTTTACTGTTTAAATTCAGTTGAATGCATTGAATTTTAAAAAATTGTCTTAAGTTACCAAACATTGTTATCTTCCAGCAAATTATCAGCAGGCTCCCTTTTTTTTTTTTTTGAGACAGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCGATCTCAGCTCACTGCAAGCTCTGCCTCCCGGGTTCACGCCATTCTCCTGCCTCAGCCTCCCGTGTAGCTGGGACTACAGGTGCCTGCCACCACGCCCAGTTAATTTTTTGCATTTTTAGTAGAGACGGGGTTTCACCGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGAGCCACTCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCCCTGCACCCAGCCTATCAGCAGGCTCTTAAGGCTACTTCCAGCTACACTTTCTTTCCCCATGCATGCATTTTCCATGTTTCCACAACTTCTTCATTTCCCTTCTGTGGGCTCATAGTGTTCCCTTTGCTTTCATAGGCCACAGTTAACTAGCTATTTGAGACATCAAAAGCTGAAGAAGCCATGGGAGATGGCAATGTTTTCTTCAGATGTCCCTTAAAACGTCATTAAAGCACCCTAGGTTGGCAAAAATTTAGGAGGTAACACAGATACCAAGGTCAACTTCAGCCAGTTTTTCTATTGCTTTGCCTGTTTCTATTGGCTGAATAAGAAGTTCGCCTCAAAGAAGCCCCAATCTAAATCCTTACCCCCATCTCCCAGTCATTTAACAGCAACAACAAACATGCCGGTTCTAGGGAATCTGTGTTTAGCACAATTAAATAGCAAGATGAACCAGACGTGGCCTTTGCTCTCAAGGGGCTTGCTGTCAGGGAGTGGACATCTCAGAAACATTCTAAGGGAGGCATAAGCCAAATGCTAAGAGAGCACAACAGGGAAGCAGCCGGGCCACAGGTGAGAAGACGAATTCTGGGAGATGGAGGTCAGCCCAAGGGCCCACTGCTGTTGTGGGAAACCCAGAATAAGGAAGGGCCCAGCTCTCCAGACCCATACCACTCCCCTCTCCCACGTTTTCTCCAAGATGGTTGTCAGTGCCCTGCTTTTCTTACTGTTTTTGCCTCTGGGGCTCAGATAACATGGAGAATGCTTATCTTAACCCGAACTGCTACCTACCACTCTCAAAAGCCCACCCAAGACACACACACTTGTTCTATCACAAGGCTACTGCTTCTTAACGCTTCTTATTTTAGAAAAGACACCATTAAGTTTACTTAGATTCATAGTAAATTTTTGCAATTAAGAATTATTCCTTCAGTAAAGTTTAAAATCCGGAAGCCCTTTTGTAGTGAAGTTCCTTTTCCCTCTATTTTGGCACCCAGATCATTTTTTTCTTTTTTGAAATGGAGTCTCTCTCTGTCACCCAGCCTGGAGCCCAGATATGTGGTCTCAGCTCACTGCAGCCTTTGCCTCCCAAGTTCAAGTGATTGTCCTGCCTCAGCCTTCTGAGTAGCTGGGATTACAGGCACACGCTACCACGCCTGGCTAATTTTTGTATTTTCAATAGAGACGGGGTTTCCTTATGTTGGCCAGGCTGGTCTTGAACTCCTGGCCTCCAGTGATCCACCCACCTCGGCGGCCTCCCAAAGTGCTGGGATTACAGATGTGAGCCACCGTGCCCAGCTAATTTTCCTAAGTTGAATGTGCATGTGTTTGTGCACATGGATATGTGCACATGAAAGGTTCCCTTCCACATCATCTCCTCTAACAATTGAAATACTCCTGCAG
Seq C2 exon
TCTCAGGCATGCTGGAACATGAAACGATTCAGGGCGTGTCTGGGGTGAAGCCCACAGGGTTGAGAAAGCGAACCTCCAGTATCGCCGATGAGGGCACCTACACACTGGACTCCATCCTCCGGCAGCTCAACTCCTTCCACTCGGTCATGTGTCAGCATGGCATGGACCCTGAACTGATCAAGCAGGTGGTCAAGCAGATGTTCTACATCATAGGGGCCATCACCCTGAACAACCTTCTCCTGCGGAAGGACATGTGCTCCTGGAGTAAAGGCATGCAGATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197535-MYO5A:NM_000259:37
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.039 A=NA C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0184314=DIL=PU(31.1=34.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
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