Special

HsaINT0108179 @ hg38

Intron Retention

Gene
Description
myosin X [Source:HGNC Symbol;Acc:HGNC:7593]
Coordinates
chr5:16681871-16683935:-
Coord C1 exon
chr5:16683880-16683935
Coord A exon
chr5:16682014-16683879
Coord C2 exon
chr5:16681871-16682013
Length
1866 bp
Sequences
Splice sites
5' ss Seq
TAGGTAAGC
5' ss Score
8.89
3' ss Seq
CTTCTCATCTTGTGGCTCAGACC
3' ss Score
5.81
Exon sequences
Seq C1 exon
GGCACCTTGGATGTGGGGCTGATTGATTCTGTGTGTGCCTCTGACAGCCCTGATAG
Seq A exon
GTAAGCTCAGATGTGGCTCTTAACAAAAACAGCTCATCACCTGTGTGTGTCCACAGGTGTCTGTGCTGCTGGGTCACGACCCTCTTCACAGGGCTGTGAAATCACGCAAGGCTGTGTGTTCCCACCTTGTCAACCCCAGCAATCCAGTCTTCCTTCTTGGTACCCAATTTTACATCACCTGGAAGTCTCCTTCTCTGGGTATCTTTGGAGTCCTGGGGAAAACCGTGGGAACCTGGACAATTTTAAAAAGCATGAGGAATATTTTTAATGTGTATACAGGGACAAACTTGGGATTTATACAGGAAGAAAATGCCTGTTTAGGAAAATGATATTCCAGCAAAGGGGAAGGGAGTCATTCTCCTTTCTGAACTTAACGATAAACTTGAAAAGGATTTTGATGATAATGTATATGTAGAGTATTAATAAACCACAAACATTGATTTTCCTTGACATTTCTTCTTTCTTGGCACCCTTTTTGGTTTTGATTTTTGAAGGCAAATCATCTTTGGAGATGATCTTACGCGTCTTTGTGCCCAGTGAACTTCATCTTTATTGTCTCTGTTTTTCTGTATTATCTTGTAAGTTCTACTTCTGGCCTGCAGCAGAATTTAAGAAAAGTTTCTCTAGGACGGACCAGAGAAAGAATCAAAATTGTCTTCTGCCCTCAGTAAGATGCTGGAAAGTGAATACGAGTGTGTTAAAATTGACAACAAAATATAGTGCCTCCTTGGCAGAGTTAGAGTGCTGGGGTCTCTGTCAGTCACCCTCCCGTTGACAAGAGCCCTTCTGAACCATGGGTCCTTTGTTTTTAGTAGTCAGCTTGCACCCCTTATAACTGGCTCAGGAATCTTTAACACGTATGTGTCATATCCGTAATCAAAGCCCTGGTGCTTCTTATTCTGGTATGTGAGTTTCTACCTTACCTTCTCCACATCTTTACTCTCCCAAGCCCTTCACTCCTCCAGGCTGGGCATGTGATGATCCATCCTTAGAATTTTGCATCCTCATTCAGGGTTTTCTCTCTTCCTCAACTGGCCACTTTTCTCCCTTGCCAACTATAGAAAAAGGCTTTTTTTATTTTTTATTTTTAAGGGGCACCTCAAGTTTAGCCTGTTTGCATAGCTTTTCCTGTGTCCTGCAGTCCAGTTACTCTTTTTCTTAAATTTTTGTGTCACCTAACTACAGTGAACATTTGAAGACTTGCAAGAAAGAGTTCACATTCTCTAGCTTAAGCCGTTAGATAGAGGAGTTAGTATTTATATTAGCAAGGGCCTATGAGAGAGGTTCAGGGCATTTCCAGACAAAAAGAGGTGAGGGAGAAAGTAAATTTCCATTATCACGTTATCCGTGACTAGGAAATGCACCCTTGTTAGATCACTTTGGAAACCCGGACCCAGGTGGCTTTTTGTATAAAGCGTAATCAAGCATTTAAGATGCTCCACCTACACCTATTTACTGATCCTCTTTTATTGCTGGTGTCTGACATTTCATTACCAACCCACAGAAATATTACCCAAGGCAGGAAGAAATTGACTTTGGAGAGGCATCAAAAAAAAATTTTCCCTCATGGTCACCTTGTTTAGCCTTCCCGGAACTGAGTTTCATCTGGAAAGTTTTGCATGAAGAAATGTTTTCCCTTCCAGGACCTTCAGAATGAATGTGTTGCTCCAAGTTTAAAGGTTAATGATGCGTAAAAGAAATTCTGCAGAAATGAGCAACGTTTGCCTTAATAAAAGCACAGATAGCCTAGCAGTGTATATCCCGTGACCCAGAAGCCAGGAAGAAGGCACTGAGTCTCGGTTCACACAGAGGTGATGCTGACGGTAGGGCTAAGGGGCTTTGTTTCCTTCTCATCTTGTGGCTCAG
Seq C2 exon
ACCCAACTCGTTTGTGATCATCACGGCCAACCGGGTGCTGCACTGCAACGCCGACACGCCGGAGGAGATGCACCACTGGATAACCCTGCTGCAGAGGTCCAAAGGGGACACCAGAGTGGAGGGCCAGGAATTCATCGTGAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145555:ENST00000513610:30
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:
NO
A:
NA
C2:
PF0016924=PH=PU(3.8=8.2)


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:
GCACCTTGGATGTGGGGC
R:
CTCTCACGATGAATTCCTGGCC
Band lengths:
198-2064
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