Special

HsaINT0108177 @ hg38

Intron Retention

Gene
Description
myosin X [Source:HGNC Symbol;Acc:HGNC:7593]
Coordinates
chr5:16683880-16685831:-
Coord C1 exon
chr5:16685738-16685831
Coord A exon
chr5:16683936-16685737
Coord C2 exon
chr5:16683880-16683935
Length
1802 bp
Sequences
Splice sites
5' ss Seq
GTGGTACGG
5' ss Score
6.61
3' ss Seq
TACTTTTTGTTCTTTTCCAGGGC
3' ss Score
11.41
Exon sequences
Seq C1 exon
CCAGTGGTTCAGCGTGCTGAGTCAGGTCCACGCGTCCACGGACCAGGAGATCCAGGAGATGCATGATGAGCAGGCAAACCCACAGAATGCTGTG
Seq A exon
GTACGGGAGCACTGTGTGGGATGGGGGTGGGGCGTCTAGGGGCAGGGACGGGGAGGGCGTCAGGATGGTAAAAAAGGGAAAGATTGGGAATTTCCAGACAGTCTTTTTTTAAAAGGTAAATATAGAATAATTAAGGAGAAAAACAGGACCATTTGAGTTTAGAATCAATACAATAATAAATATAATAAGTGGTACAATATAATACAATAATAAATACAGTAAATTAAGTTGGACACTGTGGCTCATGCCTGTAGTCCCAGCACTTTGGGAGGCTGAGGTGGGAGGATCATTTGAGGCCAGGAGTTCAAGACCAACCTGAGAAACATAGCAAGACACTGCCTCTATGAAAAAAATTAAAAATTATCCAGGCATGGTATTATGGGCCTGTAGTCCCAGCTACTTGGCAGGCTGAGGCAGGAGGATTGCTTGAGCCTGAGAATTCGAGGCTACAGTGAGCTATGATTGCGCCACTGAACTCCAGCAGCCTGACCCTGTCTCCTAAAAAAACAAACAACAAAAACGAATAAATTACAGAAGGTTGTAAGTAGTAATACATTCCAGTTCTCTCACCTCAAACCTTTAAAAGAACAAAAGAAATAATCCTACTTTTTATGAAGTCACGGAAGTACACATCACACTTACTCTTCAGAGGACTTGGTGAAATCTAAATTGTATTCTTATTTTTTTTTTTTGAGATGGAGTCTCACTCTGTCACCCAGGCTGAAGTGCAGTGGCGAGATCTCAGTTCACTGCAACCTCCGCCTCCAGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCTTGCCGCCACACCCGGCTAATTTTTTGTATTTTAGTAGAAACAGGGTTTCACTATGTTGCCCAGTCTGGTCTGGAACTCCTGAGCTCAGGCAATCCACATGCCTCAGCCTCCCAAAGTGGTGATACAGGCGTGAACCACTGTGCTGGGCCGAAATCCAAATTGTATTCTTTGTCTTCCCTCTATCCCAGACACAAAGTTACAAAACCCTGCTTTGGAAACCAAGTTTTATTTCCTCATCAGAAAATCTTGAAATAAAGTTTCTTAGGAGAAGAAGTGTAAGATTTAATTAAAGGACACAATATAATCAGGAAATTTGTACTATTGAAAGAAGGTCATAAACACTGTTCACTGAACATATTTTAAGAATAAGAGGGGCCAGGTGCGGAAGCTCAGACCTGTAATCCCAATACTTTGGGAGGCCAAGGCGGATGGATCACTTGAGGCCGCCAGGAATTTGAGACCAGCCTGGCCAACATGGCGAGACCCCATCTCTACTAAAACACAAAATTATCCAGGTGTGGTGGCCCACACCTGTAGTCCTAGCTACTTAGGAGGCTGAGGCACGAGAATCACTTGAACCTGGAAGGCAGAGGTTGCGTTGAGCTGAGATCACACCATTGCGCAGCCTGGGCAACAGAGTGAAACTCTGTTTCAAAAACAAACAAATTAAATTAAAATAGAGGTACTTGTAGAAAACTTAGTTAAAATATTTTTAAAAACAAAGAAATAAATTATTGAAAGGTTAAGAGGTAATGATTAACTTGTAATTTTAAAAAATAAATGGCCTATAGATTCTGCTCCGTGTAGAGGCTATTTGTACTCACACAACAGAGGAGTCGTCTCATAGATAACTATTATTTTGAAGTTAAAAAGAAAAGAGCCTTTTCTGTCTGATTGGGAGTTGTGGGCTAGAGGTATTACTGTAGTGTGCACCCTACTTTAGTGCTTCTCTCATTCTGTTTACTTTTTGTTCTTTTCCAG
Seq C2 exon
GGCACCTTGGATGTGGGGCTGATTGATTCTGTGTGTGCCTCTGACAGCCCTGATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000145555:ENST00000513610:29
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.500 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0016924=PH=PD(11.2=34.4)
A:
NA
C2:
NO


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:
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