Special

HsaEX6094932 @ hg38

Exon Skipping

Gene
ENSG00000182472 | CAPN12
Description
calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]
Coordinates
chr19:38742410-38752098:-
Coord C1 exon
chr19:38751998-38752098
Coord A exon
chr19:38743033-38743102
Coord C2 exon
chr19:38742410-38742528
Length
70 bp
Sequences
Splice sites
3' ss Seq
GAATCCCCCACCACCCACAGGAG
3' ss Score
5.17
5' ss Seq
TGGGTGAGA
5' ss Score
6.04
Exon sequences
Seq C1 exon
GGGCAGCATCAGTCTTCAGCTGCTAAGCCGAGAAGATCTGGGAAGGAGTCAGTCAGAGAGCCTTGGGCCAGAGTTCCAGGGGCTCTGGGAGTGGCTGCCAG
Seq A exon
GAGTTCTGTGCTGAGCCGAAGTTCATCTGTGAAGACATGAGCCGCACAGACGTGTGTCAGGGGAGCCTGG
Seq C2 exon
GTAACTGCTGGTTCCTTGCAGCTGCCGCCTCCCTTACTCTGTATCCCCGGCTCCTGCGCCGGGTGGTCCCTCCTGGACAGGATTTCCAGCATGGCTACGCAGGCGTCTTCCACTTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182472-'5-5,'5-4,7-5
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=NA A=0.030 C2=0.000
Domain overlap (PFAM):

C1:
NA
A:
PF0064816=Peptidase_C2=FE(21.7=100)
C2:
PF0064816=Peptidase_C2=FE(13.1=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GCCGAGAAGATCTGGGAAGGA
R:
AGCCATGCTGGAAATCCTGTC
Band lengths:
171-241
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains