Special

HsaINT0027365 @ hg19

Intron Retention

Gene
ENSG00000137225 | CAPN11
Description
calpain 11 [Source:HGNC Symbol;Acc:1478]
Coordinates
chr6:44137018-44137712:+
Coord C1 exon
chr6:44137018-44137268
Coord A exon
chr6:44137269-44137642
Coord C2 exon
chr6:44137643-44137712
Length
374 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGC
5' ss Score
7.93
3' ss Seq
CCTTTATTCCTTCACTGCAGGAT
3' ss Score
10.53
Exon sequences
Seq C1 exon
AGCCCACTTTTACTGATACGGGAATGGTGGCTCACATAAACAACAGCCGGCTCAAGGCCAAGGGCGTGGGCCAGCACGACAACGCCCAGAACTTTGGTAACCAGAGCTTTGAGGAGCTGCGAGCAGCCTGTCTAAGAAAGGGGGAGCTCTTCGAGGACCCCTTATTCCCTGCTGAACCCAGCTCACTGGGCTTCAAGGACCTGGGCCCCAACTCCAAAAATGTGCAGAACATCTCCTGGCAGCGGCCCAAG
Seq A exon
GTGGGCACTGGAAGGGAGGCATGGACTCATGGATGGAAGGGAGCTTGTAGTGATCCCTCTATCACTTTTAGAATCTTCAATCTTCAACCCCCCACTACCCCATTCTGACCCTGGCACTAGGCCCCACCTTCATCAGAGCTGGGGACAGTTCTGAATATGCTTAAGCCAAACCTCCTAGGTAACCCTAAGGAAATCACCCACCAACCTCTGCTATCACAAGCTGCAGCTATGCCAAGTTGGTCCTGTACCCTCTCCCTGCCCCTCATATCTGTTCCCCTGGAACTTCAAGGTGGGCATCATTCCCCAGCAAAAGTGGGAGAAAGGTGGGGAGGGGGTGTCCTGGGCCCCCTGAAACCTTTATTCCTTCACTGCAG
Seq C2 exon
GATATCATAAACAACCCTCTATTCATCATGGATGGGATTTCTCCAACAGACATCTGCCAGGGGATCCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137225-CAPN11:NM_007058:3
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.250 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0064816=Peptidase_C2=PU(11.3=40.5)
A:
NA
C2:
PF0064816=Peptidase_C2=FE(31.1=100)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GCCCACTTTTACTGATACGGGA
R:
GAGGATCCCCTGGCAGATGTC
Band lengths:
319-693
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