Special

HsaINT0108821 @ hg19

Intron Retention

Gene
Description
myosin VB [Source:HGNC Symbol;Acc:7603]
Coordinates
chr18:47365514-47367824:-
Coord C1 exon
chr18:47367735-47367824
Coord A exon
chr18:47365665-47367734
Coord C2 exon
chr18:47365514-47365664
Length
2070 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
GCACGCCTCTCCCTCTGCAGGGC
3' ss Score
10.74
Exon sequences
Seq C1 exon
AAGCACAATGATGACTTTGAGATGACGTCATTCTGGTTATCCAACACCTGCCGCCTTCTTCACTGTCTGAAGCAGTACAGCGGGGATGAG
Seq A exon
GTGAGTGGGGAGCCAGGCACCCAGGAGGCATTCCTGCTTCATCCAAATGTGGTTGAGAAGTGCTTTGTATACCCTCAGAGGTCAGTGGGGTCTTTGGAGCACCCTTGGGGACCTCAGACCGTGGGCACACCTTATCATGCCTCGTGGCTGGAAGCAGCAATAAGGCCAGCCACAGGAGACCTGCCTCTAGGAGGCCTTGATGAGCCCAAGGGGCCCCAAAAAGCACTCCTGGGTTATGTAAGTAGAGTCTGCATAACCCATGATCAATAGAGGCCCTGGGAGTCTCCATGAAACTCTTGTAACCTGACATTTCTGTATCAGCTCTAGAAGCCCCACTGCAGTGGATACTGGCAGGGAGCTCAGTTGCCTAGTGGGTCACCCTGTCTCCTAAGCCAACTGATTAATCTGTCCATTTCAAGATAGACAAAGATGGCCACAAGAACAGAGGCACACCATAATCAGAACTACGTGTGTGCAAACTGACCTGGAGGCCCAGCTCCATGCATTTATCCAAATTGGATTCCTTGACCTGAGGCCCAACTACTAACCCCATCACTTCACAATCCACACCGGACCTGTAAGGCCCAGCTTTTTCTGGAACTCACATTCCTAGCTTTGGTCCCTGAAAGAACTTCTCCCATGCTCTGCACTCTGCCCAATGACCTAGTAATATGTGGCTTGTTTCCATTCTAGTTTCTCTGGTGAGAATCCCAGCTTGTTCCAGATATGCCCGCTCACAGGTTCCTGTAGGTCTTCCAACTTTTCTTCCCCTTCCTTTCACATATCTCACCATCCACCCTTCCCAAGGTCAAGACATAGTGTAAACCAAAATAGTGCGACCATTTTTAAAGCTTTATTCCATCTTTTGTGCCAGAACCAATTTTGACAGACTCTTCTCCCTGGGTTAGTAAAAGGATATGCCCTTCCTTTCAGTCTTACCTTCTTTGCAGTTGGCTTGACGCCATCTCTCTCCTAAGAACCAGCACTTCATTTGATGGCCTGCTTTTATTATAAAAGAGATGGGCCAAAGGTTAAAGAAATAGCCATTTCAAACCCCATGACTTCTGTTACAAAATCATAATATCCAAGCATTTACTTGAAGCATAGAACTACATGTAATGTTATTTCATTGAGGTCCATCACTTTACCCAATGTTATACACATTCTAAATGGGAGGTTATATAAGGCTAGGGCAGGACCTAGAACTCCATTACATTAGGTTGTGGTTACATGTGCTCATATTCTCTGGGTCAAGAGCTGAACCACAGCATGACCAGATCCGTGTAGTCCAAATAACAAGGAAGAATGATTGACTCTATCTTCATCATTACAATTATCCCCTTTTCTGCCTGCTTTTTTTCATATTAAGATGGCTTTGTATTTGACACAGTACAACAGGCCTTGCTGAAGATGGTTGCCCTTTTGGGAGCACTAATCTTTTTGGCAGATACTGGTTTCCCTAGGCCTGAATGAAAAGGACATTGGTCACATGAGCCCTTCTGATATCAGCAGTTCCCTTAACTTACATGTGATTTCATCTGATTAATACAGAAAGCTAAGAGGACACAGTGCGGTAGCTATGAAATCACTTTAGTTCATCTATTAATTCTGATAACCAGTGATAGAATCTGTATAAAATTTCTCCTCATACAAGCGTATAATCTGGCCCATGGCCACACTCCTTTAGAGGCTGCACATCATCTAACATTTTAGGGGGACCTGATATATTGAGGAAAGCGCTGGATGAAGGGAAAAAGCAGGGATCCCTTTCTCTGGACCTGGTACCAACCTAGGTTTTGCTACCGTAGGGAAATCACTTCGCCTCAGGGATTTGGACTGAGCGATTCAGGCTTTCTCTCTCATGTTGAGTTTTTCTACATCCTTCAAGTTCAAGGGTCATCAATGAGGCCTCAAAGAACTGACAGGCTTTTGTAAAACATCATCTACATAGGGAGGGCCTGAGTAGGCCCCCTGCCCACCAAATAGATGACTAAAGTTACCAGAGCCCTGGAAGTTGTGCTGGGCCCAGCAGACCAGAGAACTCAGTAGTGCACGCCTCTCCCTCTGCAG
Seq C2 exon
GGCTTCATGACTCAGAACACTGCAAAGCAGAATGAACACTGTCTTAAGAATTTTGACCTCACCGAATACCGTCAGGTGCTGAGTGACCTTTCCATTCAGATCTACCAGCAGCTCATTAAAATTGCCGAGGGCGTGTTACAGCCGATGATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000167306-MYO5B:NM_001080467:35
Average complexity
IR-S
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:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion 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