Special

HsaEX0012360 @ hg19

Exon Skipping

Gene
ENSG00000162949 | CAPN13
Description
calpain 13 [Source:HGNC Symbol;Acc:16663]
Coordinates
chr2:30973969-30977230:-
Coord C1 exon
chr2:30977156-30977230
Coord A exon
chr2:30975919-30976064
Coord C2 exon
chr2:30973969-30974117
Length
146 bp
Sequences
Splice sites
3' ss Seq
TGTATATCTGTTTTTAACAGGAT
3' ss Score
9.63
5' ss Seq
CAGGTAATC
5' ss Score
6.99
Exon sequences
Seq C1 exon
GTCTCAGGAGTGGGAGGAAACCTGTGATCCGCGGAAAAGCCAGCTACATAAGAAACGGGAAGATGGCGAGTTTTG
Seq A exon
GATGTCGTGTCAAGATTTCCAACAGAAATTCATCGCCATGTTTATATGTAGCGAAATTCCAATTACCCTGGACCATGGAAACACACTCCACGAAGGATGGTCCCAAATAATGTTTAGGAAGCAAGTGATTCTAGGAAACACTGCAG
Seq C2 exon
GAGGACCTCGGAATGATGCTCAATTCAACTTCTCTGTGCAAGAGCCAATGGAAGGCACCAATGTTGTCGTGTGCGTCACAGTTGCTGTCACACCATCAAATTTGAAAGCAGAAGATGCAAAATTTCCACTCGATTTCCAAGTGATTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162949_CASSETTE1
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.615 A=0.000 C2=0.130
Domain overlap (PFAM):

C1:
PF0064816=Peptidase_C2=FE(8.4=100)
A:
PF0064816=Peptidase_C2=PD(6.0=36.0),PF0106717=Calpain_III=PU(12.4=34.0)
C2:
PF0106717=Calpain_III=FE(35.8=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCAGGAGTGGGAGGAAACCTG
R:
TGGAAATCGAGTGGAAATTTTGCA
Band lengths:
211-357
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development