Special

HsaINT0027477 @ hg38

Intron Retention

Gene
Description
calpain 3 [Source:HGNC Symbol;Acc:HGNC:1480]
Coordinates
chr15:42392639-42394341:+
Coord C1 exon
chr15:42392639-42392722
Coord A exon
chr15:42392723-42394255
Coord C2 exon
chr15:42394256-42394341
Length
1533 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGC
5' ss Score
9.85
3' ss Seq
GCTCTTTCTGTGTGCTTAAGGTC
3' ss Score
7.38
Exon sequences
Seq C1 exon
ACAATCATTCCGGTTCAGTATGAGACAAGAATGGCCTGCGGGCTGGTCAGAGGTCACGCCTACTCTGTCACGGGGCTGGATGAG
Seq A exon
GTAAGCCTGGTGGGGCTTGGTGGGGCAAGGGCACCCTCCTGGGTTAACCTCATGAAGTCAGGACTTAGCTGTTGGGGCCCCTTCCCTGTCTGCAGAGCTTGCCTCCAATCAGGACATTCAGTTCAAGGTCCAAGCCACGCCTGGGAGCAGAGGGGCCTGTGAAACTGGTAGAGGTGGATCCTGCCACAGTTGGTGCACAGTTTATCTTTGCTTTTCGTGCTAAAGATGGCAATTTTTCCAACATTTCCAATGAACAAATTGAAATATCACTTAACTTTGCTTTTACAAAGTTGGTTTCATGTGTTCTTGAGCTTCCTGTTCTCTCGTGTTCAGATAGCTACAGTTGTCTCTGGGTAGCCACGGGGACTGGTTCCAGAAGCCCCAACAGTAACAAAATCTGCAGATGCTCAAGTCCCTTCTGTAAAATGGAGTAGTATTTGCATATAACCTATGCACATCCTCCCATATACTTTAAGTCATCTCTGGATTACTTACGATACCTAACACAATGGAAATGCTATGTAAATAGTTATTGCACTGCATTGGGTTTTTTTGGTATTATTTTCTGTTGTTGTATTATTATTTTTTCTTTTTTTGAATATTTTTGATCCACAATTGGTTATATGCCAAAGCCATGGATACGAGAGGCTGACTGTTCTGTTTTGCTCCTTCTGGGACTTCTGGGTTTTCCTGGACCATGTCTGAGACAGGAACGTTGTAAGACCTGTTGCACACAGTTGGGCAGGTTGTGCCCTGTACAGAGGGATGGGCTGAGAGGGGCAGTTGCCTGCATCACCCATTGCAGCAGACTGGAGGGAGTCTGCTTGTTTGTAGTTCCTCAGTCAGCAGGGGCCTTTTGTCTTTCTTTCTTTCTTTTTTTTTTTTTTTTGAGACGGAGTCTCACTCTGTTGCCCAGGCTGGAGTGTAGTGGCACAGTCTCGGCTCACTGCAATGTCCGCCTCCTGGATTCAAGCGATTTTCCTGCCTCAGCCTCCTGAGTAGCTGGGATTACAGGCGCGTGTCACCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGATGGGGGTTTCTCCATGTTGATCAGGCTGGTCTCGAACTCCTGACCTCGTGATCCGCCCACCTCGGCCTCTCAAAGTGCTGGGATTACAGGCGTGAGCCACCACGCCTGGCCAGCAGGGGCCTTTTTTCTAATTTATATGAAGACACCTAATTTATATGTGTTAGCAGGGCCCTACTGTTTATGCCTCACCTCCTCCCCCGAAGCTCATAACGGCAGGATGTTCCTGAGAAAATTGCCTCTTAGAAGATAGAGAGGAGATGGCCAAGCCCTAAGTTAGGCAGACTCAGGAGGAAAGGTCTGACCCACCCCCTGCCATTCCCCAGCACACTTGTGATTAATCTCCTTGGCCAGAGCCAGGCAGAACACCCTCGCGTAAGAGATTTGCCCCCCAGCCCCGTCCCAGCCCTCAGCAAGACAGAAGATTCCCTTTCCAGAGAGGCTGCAGAGCATGAGAGCTCTTTCTGTGTGCTTAAG
Seq C2 exon
GTCCCGTTCAAAGGTGAGAAAGTGAAGCTGGTGCGGCTGCGGAATCCGTGGGGCCAGGTGGAGTGGAACGGTTCTTGGAGTGATAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000092529:ENST00000318023:6
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.036 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0064816=Peptidase_C2=FE(18.2=100)
A:
NA
C2:
PF0064816=Peptidase_C2=FE(18.9=100)


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