Special

HsaINT0107588 @ hg38

Intron Retention

Gene
Description
myosin heavy chain 14 [Source:HGNC Symbol;Acc:HGNC:23212]
Coordinates
chr19:50252639-50255318:+
Coord C1 exon
chr19:50252639-50252753
Coord A exon
chr19:50252754-50255219
Coord C2 exon
chr19:50255220-50255318
Length
2466 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGG
5' ss Score
9.2
3' ss Seq
CATCTGTCCTCACTCCCCAGAAC
3' ss Score
10.16
Exon sequences
Seq C1 exon
GTCGACTACAAGGCCAACGAGTGGCTGATGAAAAACATGGACCCTCTGAATGACAACGTCGCAGCCTTGCTCCACCAGAGCACAGACCGGCTGACGGCAGAGATCTGGAAAGACG
Seq A exon
GTGAGGACCCACTTCCCCCACCCCGGCTCTAGGGGTCTGTGCGGCCATTCTCCAAATCCACAGCGTGAGCACCTTTGTTTCAGAGGCGGAGGTCTGAACCTGAGTTTTCTGCTCAGACCCAGAATAGCCAGTGTCACAAATAGTATTTCAAATCAGTGATGGATGGATCCATAGATTAATTGATTGACTATTGATTTGATTGATAAGCCAGCATCCTTCTCAAGGATAAAGCACTCCGCCTTAATCAGAAACGTGGCAAAGATACCCACTAACACTACTGTTAAACATCGTTTTTTTAGCAATACTAGCCTATGCAATCAGACCAGAAAAAGTATGAATATCGAACAGGAAGAAGTAAACTTATTATTTTTAGATGGCCTGTGTTCCCTAAACAATTAGGAGATTTGGCTGGGCATGGTGGCTCACACCTGTAATCCCAGCACTTTTGGGAGGCCAAGGTGGGCGGATCACTTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAAGTACAACAATTAGCCAGATGTCCTGGTGCATGCCTGTAGTCTCAGCTACTAGGGAGGCTGAGGCAGGAGAATCGCTTGAATCTGGGAGGTAGAGGTTTCAGTGAGCCAAGATTGTGTCACTGCAATCCAGCCTGGGTGACAGTGTGAGACTCTGTCCCAAAAAAAAAAAAAAAATTCTACTGAGAAATAATTTATAACAATAAGAGAACACAGAATGATGATCTTTTGCAGGTCAGTCAACTTTTAGGCTTTGCTTTCTTTGTTTTCTTACAAAGTTCCCTTCACGCCCCCAGGGAAGAAGAAAGAAAAAACAGACTGAGATACAGTTTTGGAGGGCTTTCCTGCCCCCAAAAGGCCCCCATGAGTGTGACTGTCTTTTTGGATTGACACTTCTAGGGGTCATAGGCAGAGATGCCAAATGCCCTGTGGTAGGACTCTGACCTTTTCCAAGCCTTTTCTGCCACTGCCCCTGCCCCCCCATCCTTAGAGGAGGTTTGAGAAATGGTTTTAGAAAGCTGGCAGAACTGGCATCCTGTTTTTTCCAGGTTCCAAGTTTCTGGCATTTGTCAGTTTGCCTTAATCTTTTATTGACATGAAAAGGTAGCTGTAGAAATACCAGTCCATGCAATTTGGCAAGAAAACAAAATGAGCGGCCAGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCAAGGTGGACGGGTCACCTGAGGTCGGGAGTTTGAGACCAGCCTGACCAACATGGAGAAACCTCATCTCTACTAAAAATACAAAATTAGCTGGGCGTGGTGGCACATGCCTGTAATCCCAGCTACTCGGGGGGCTGAGGCAGGGGAATCGCTTGAACCCGGGAGGTGGAGGTTGTGGTGAGCCGAGATCGTGCCATTGCACTCCAGCCTGGGCAACAAGAGTGAAACTCTGTCTCAAAAAAAAAAAAAAAGGAAAAAAAAAGAAAACAAAATGAGCAAGGTGAGTGGTTCCCAAAACACACTCACAGAGCAAAACAGCATGGAGGGTCTTGATCTTGTGAGCTCATGCTAGAAAGATAGATTTTATTTTTATGTCTCATATAGTATTTACACAAGGAGATTGGAAAGCAGAGTTTGATGTTCAGGAACAGAACCAGATTATGCTACGAGAATCATCTCCCGGCTGAAAATCTGCTGCCCTTTTAAAATATTTGTGCTGTCTTCATAAACACATGATTCTCCACAGTGAGCCCTCATTTGTCACACTCTGTGTGTGCCTGACTCTCAGAGGGTTCCAAAAGAAAAAGTGGAAGCTGCAAAACCTCCTGGCTCAGCCTCCCGAGTAGCTGGGGAGCTGCCATAATGTCACTTCCTCCATAATCCTCCTAAACAAAGCTAGTCACAAGGTCTTCCCAGATTCAAGGAGCTGCAAGACACAGGCAAAGGGTGTCAATACAGGGGAAAGTGGGGAATCGGGGCCATTTTTGCCCAATCTCTGCTAGAGCTGCTTTGAGCCCAGAATTGGATGCCCAGCATCCTGACAGCCCAGGGAAAAACGGAAATGAGATTAGCTCTCCTCTGAGAGGCAAAAACAACAAGTGGCCTGGGAGCATCAAGTTCATTCTTGAGCTTCCTGGCAGCCAGAGCAAAAAGGGCAACCTACTAAAACAGACACAACCTCTAGAGGGAGAGATTTTTTATTCTTTGCACTGAATTCTTACAGAGGACATTCGTCCTTTTGGCCAACAGTGTGTGGATACAAAGATGAACAGGAGTTCAGAAGTTTATGGCCAACATTCTGGTTTTCCATCTTGCTTTGCTCTGTACTGTTGACTAATAACCCTCTCCTCTTTTTCTTCCTGCCACCTCCTCTCCTTCCCCTCTTTTCATGCATCTCTCTCCGCCATCTCTCTGCCATCTCCCCTCCACCCACCCACACATCTGTCCTCACTCCCCAG
Seq C2 exon
AACATGGGGGCTTCCAGCAGTTCTCTTTCCTTGGCTCCTTCCCACCGTCGCCCCCAGGATCTGCAGAGAGGTGCAGCTCTGCTATTTCTCCGCCAGGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105357:ENST00000601313:16
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.015 A=NA C2=0.265
Domain overlap (PFAM):

C1:
PF0006316=Myosin_head=FE(5.6=100)
A:
NA
C2:
PF0006316=Myosin_head=FE(4.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping 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