Special

HsaINT0108909 @ hg38

Intron Retention

Gene
Description
myosin VIIA [Source:HGNC Symbol;Acc:HGNC:7606]
Coordinates
chr11:77192051-77194524:+
Coord C1 exon
chr11:77192051-77192278
Coord A exon
chr11:77192279-77194353
Coord C2 exon
chr11:77194354-77194524
Length
2075 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
CGAGGCCTCCCCCCACCTAGGAG
3' ss Score
5.93
Exon sequences
Seq C1 exon
GTGTCCTCCCTGGGCAGCGGCAGTGACCACGTCATGGACGCCATCTCCCAGTGCGAGCAGTACGCCAAGGAGCAGGGCGCCCAGGAGCGCAACGCCCCCTGGAGGCTCTTCTTCCGCAAAGAGGTCTTCACGCCCTGGCACAGCCCCTCCGAGGACAACGTGGCCACCAACCTCATCTACCAGCAGGTGGTGCGAGGAGTCAAGTTTGGGGAGTACAGGTGTGAGAAG
Seq A exon
GTGAGTGGGAGGGAATCTTCCGCCAGGCTGGCTTGGCTCACAGCCTCCTGCTTTCCACGTTTGGGCTGAGTGCTCCTCTGTGAGCCATCATTAGCTCAGGCTGGGGTGAGCCTGACTGCAACCAGGCACTCTTCAGGCTCCTGGATGGACACCGCCTACTTCAGGGGGCTCGTGAGGAGAGGCGAGATGGCGGGAGCAAGGGCTTCTGAGGATGTCCTGAATTCCACCAGTGGAGGAGGCCCCCACACTGCTGTAGTGACTGTGCGTGCTACAGAGGACGTGCCGCAGGACCTGCTGCACCATTCTGAGTATATCTAGTAAGCGCTGCATTAAATGAGAAATACAGCCATTCCTTGAGATCAGAATTTGCAAATGTGTATTCTTTTTTCTCCTTCTGAGGACAGGAGTTATGTGGTTGTTTTGTTTTCGATAATGGTAATGGTAGCTATGGTTCTGTTGGTGATTGTGATGGAGGGATGAGAAAGGAGGTGGTGGAAATGAAGAGGATAGTTGGTGGTAGTAACGTTGGTGGAGGTAGTGATGATGGTTGGTGGTGATGGTGGAGGTAGTGATGGTGTTGGTAATGATGATGGTGGTGATGGTGGAGGAGGTAGTGATGGTGTTGGTGATGGTGGAGGGTAGTGATGGTGTTGTTTGTGATGGTGGAGGTAGTGATGGTGTTGGTGATGGTGGAGGTAGTTGTGATGGTGGAGGTAGTGATGCTGTTGGTGATGGTGGAGGTAGCGATGGTGTTGTTGGTGATGGTGGAGGTGGTGATGGTGTTGGTGATGGTGGAGGTAGTTGTTTGTGATGGTGGAGGTAGTGATGCTGTTGGTGATGGTGGAGGTAGCGATGCTGTTGGTGATCGTGGAGGTAGCGATGGTGTTGGTGATGGTGGAGGTAGTGATGTTAGTGATGAGGTATTGTTGGTACTGATGACTATGGTAATATTGGAGGTAGGGATGATGTTAGTGATGGTGGTGGTGGTGGTGATGGTGGAGGTAGTGATGGTGTTGGTGGTGATGACAGTGTTGTGGGTAGTGATGATAGTGGTGATGGTAAAGGTAGTGATGGTGGTGTTGACAATGACAGTGTTGTTGGTAATGATGGTGATGGTGGAGGCAGTGATGGTGTTGGTGATGACAGTGTTGTTGGTAGTGATAATGATGGTGATGGTGGAGGCATAGTGTTGGTAGTGATGATGGTGGTGATGGTGGAGGCAGTAATGATGTTGGTGATAGTGTTGGCAGTGATGGTGGTGATGGTGGAGGTAGTGGTGGTAGTTTTGTTGGTGATAGTGGTGATGATAATGGTGGTATTGGTGGTAAGCAAATATTCAGGCGGAGTGCATTAGTATAGCCACATCAGTTGCTAAAATTCTGAAATATTTCAAACTGGTTGGAAAATATCTATTGCCTCCAAGGCCCCCAAGAGCCTTTCTCTATGCCCTTGCTGCTGGAGCCCTGGGGAGCTCTAGGTAGGCATCACTGGGGCTGCTGTGCACCAGGCCAGGCAGAGAAGGGGCAAATGCCCAGTGGCCACTTGGCTCTCTGAACCCTCTGCAGTAGATCCTGCCAGCTGTTAACCACTTTAACTGTCCCCCAAGTGCTTAACGGTGGTAATGGTGATGGAGGCAGTCACAGTGATGCACTTCCCTCACTCTGACCCTGCCAGCAGACCCTAGGTGTCTCCCATTCTCCAGGGCAGACACTTCCTCTTCTGCTGTTTGTCAGCTCTGGTCGCTGTCTCACAGGGCTGAGTGTGCAGTGGCTGCTCGATGGGCTGGCTTGTTTCTTTGCATCACTTCATGTGCCCCTGGGCAGAGTCCAGCTCCATGCCAGTGCCAGAGGGATCCAGGAGAAGGTGAGGGTGTGGCCCTGCCCTTGGGGAGCTCATGGTTCCTCTGAGCAGACAAGAATTCCCTGGTGAATCAGTGAGAAGCCTGGGTCCCAAAGGCCAGGCTCTGAGAGCTACAGGAGGCAGGGCCAGGAGAGGGGCCTGGAGCCTTTGGTGGTGTGGAAGGGCTTCCTGGAGGGGCCTGGGCCAATGCATGACCGAGGCCTCCCCCCACCTAG
Seq C2 exon
GAGGACGACCTGGCTGAGCTGGCCTCCCAGCAGTACTTTGTAGACTATGGCTCTGAGATGATCCTGGAGCGCCTCCTGAACCTCGTGCCCACCTACATCCCCGACCGCGAGATCACGCCCCTGAAGACGCTGGAGAAGTGGGCCCAGCTGGCCATCGCCGCCCACAAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137474:ENST00000409709:31
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.013 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF093795=FERM_N=PD(47.3=56.6)
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