Special

HsaEX6012724 @ hg38

Exon Skipping

Gene
ENSG00000162949 | CAPN13
Description
calpain 13 [Source:HGNC Symbol;Acc:HGNC:16663]
Coordinates
chr2:30758046-30764306:-
Coord C1 exon
chr2:30764132-30764306
Coord A exon
chr2:30763082-30763156
Coord C2 exon
chr2:30758046-30758137
Length
75 bp
Sequences
Splice sites
3' ss Seq
TCTGCTTTTCTGCCTTGAAGCCA
3' ss Score
7.09
5' ss Seq
CAGGTAAGG
5' ss Score
11.08
Exon sequences
Seq C1 exon
GCTGCTCGGATCCTATTCCGATCTGCACTATGGCTTCCTCGAGGATGCCCTGGTGGACCTCACAGGAGGCGTGATCACCAACATCCATCTGCACTCTTCCCCTGTGGACCTGGTGAAGGCAGTGAAGACAGCGACCAAGGCAGGCTCCCTGATAACCTGTGCCACTCCAAGTGGG
Seq A exon
CCAACAGATACAGCACAGGCGATGGAGAATGGGCTGGTGAGTCTCCATGCCTACACTGTGACTGGGGCTGAGCAG
Seq C2 exon
ATTCAATACCGAAGGGGCTGGGAAGAAATTATCTCCCTGTGGAACCCCTGGGGCTGGGGCGAGGCCGAATGGAGAGGGCGCTGGAGTGATGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162949-'18-21,'18-18,20-21
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.120 C2=0.097
Domain overlap (PFAM):

C1:
PF0064816=Peptidase_C2=FE(19.4=100)
A:
PF0064816=Peptidase_C2=FE(10.3=100)
C2:
PF0064816=Peptidase_C2=FE(10.0=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:
CTGCACTATGGCTTCCTCGAG
R:
AATTTCTTCCCAGCCCCTTCG
Band lengths:
183-258
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains