Special

HsaINT0107473 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:7568]
Coordinates
chr17:8508554-8509949:-
Coord C1 exon
chr17:8509812-8509949
Coord A exon
chr17:8508678-8509811
Coord C2 exon
chr17:8508554-8508677
Length
1134 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGA
5' ss Score
6.91
3' ss Seq
AGTCAATTTTTCCTGTCCAGGAA
3' ss Score
7.22
Exon sequences
Seq C1 exon
GACCTGGAAGAACAGCTAGACGAGGAGGAAGGGGCTCGGCAAAAGCTGCAGCTGGAAAAGGTGACAGCAGAGGCCAAGATCAAGAAGATGGAAGAGGAGATTCTGCTTCTCGAGGACCAAAATTCCAAGTTCATCAAA
Seq A exon
GTAAGAGAGTGTTCCCACAAAAAGCTGATTTTAGTTACAGAAAATATTTATATAATATTATGTTGATACACTCATTGAAAGTGAACTCAAACAGAAATTTCTCAAGATTTTAGGTTCATTTACTGAATTTTCTCTGTAAGTCTCTACTTGTATAGATTTCTAAAGATACAGGCACCATTGAATTTTTTAAACCTTATCAAATATCCTGATAATCTTTTAGACTTGTAACATGTGCAGTTTGTGCATAATGGTCACTCAATGATGACTTGTCTCCATCTGTGCAAGCATTAATTCATCCACCATTGACTGTGGGACTCTGAATACCAGGCAGCTGGGCCAAGCTCCCGGGGTGGGCACCAAGACGTGTAAGCCTTTCTGCCCTTTTGGAGTACAGTCGTGTGTTGTTTAACGATGAGGACACATTCTGGGAAATGCATTGTGAAGTTATTTTATCCTCGTACAAACATCATAGAGTGTATGGACACAAACTAGATGGTAGAGCCTGCTATACACCTAGACCAGACGCTGGGCTGATTGCATCTAGGCCACACACTTGTACAGCATGTTACTGTCCTGAATACTGTAGGCAGTTGGAACACAGTGCTAATAAGTACTTGTGTATCTAAACATATCCACACAAAAGTCCAGTAAAAATATGATAGAAAAGGTACGGTAAAAATGATAGAAAAGATTTAAAATGGCACACCTCTATTGGGCACTCACCATGAACGGAGCTTGCAGGACTGGAAGCTGCTCTGGGTGAGTCAGTGAGTGAGCGCTGAGTGAATGTGAAGGCCTAGGACATTGCTGTACATGACTGCAGACTTTATCAACATGGCACACTGAGGCTGCAGTACATTTATTTTAAAAATAGAGTAATTGCACTGTGGTGTTATGACAGCTCTCGATGAAGTTTTCAGCTCCATGATCATCTTAGGAGACCACTGTCGTGTATCCGGTTCATCATTGTCCAAAACATCGTTCTGCAGCATGTGATTGTGTACAGTCTGCTGGGGGAGGCAGTGCCGATAGAACTTATTTTCTCTCGAGTCAAAGTTGACCTTTATGAGGAATACAGAACCCAAGTGGTCATTCTGAATGGCTTTTCTGAAGCAGTCAATTTTTCCTGTCCAG
Seq C2 exon
GAAAAGAAACTCATGGAAGATCGCATTGCTGAGTGTTCCTCTCAGCTGGCTGAAGAGGAAGAAAAGGCGAAAAACTTGGCCAAAATCAGGAATAAGCAAGAAGTGATGATCTCAGATTTAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000133026:ENST00000269243:23
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.370 A=NA C2=0.524
Domain overlap (PFAM):

C1:
NO
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:
ACCTGGAAGAACAGCTAGACGA
R:
ATCTGAGATCATCACTTCTTGCT
Band lengths:
254-1388
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