Special

HsaINT0027378 @ hg38

Intron Retention

Gene
ENSG00000182472 | CAPN12
Description
calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]
Coordinates
chr19:38734319-38734870:-
Coord C1 exon
chr19:38734813-38734870
Coord A exon
chr19:38734390-38734812
Coord C2 exon
chr19:38734319-38734389
Length
423 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGT
5' ss Score
10.1
3' ss Seq
TGACTTTGTTTTTCCTGTAGCCA
3' ss Score
8.85
Exon sequences
Seq C1 exon
GAGGAAGAACTCAATGCCTCTCAGCTCCAGGCCTTACTAAGCATTGCCCTGGAGCCTG
Seq A exon
GTGAGTTGGCTGGGATAGGGGCAGGAGGAGGGGTCTTAGCCAGGGGTCCTGCAACCAGAGCCGGTGCCACCCTATGTCTATGAACCCACCGCGCTGCTGGGAGTTGGGCTCAGGAAGCCAGGGCTCAGCCTGGCAGCATCTCCCTGCAGGGGATCTTGTGTGGGCCCCGTGACCTGGGCCACGGCTGCTCGCAAGCTCCCCTTCCGCTGAAAGGCAAGGCTGCCTTGAGCACAGACTGGGCACCCCCTGCCTGGATTTGAATCCCAGCTCTGCTAGGCGCAGCAGTCACTGGCTCCCTGTGCCTCGGCTTCTATAATATGGGACTGACAACATCACCTGCTTAAGGGAGTCACATCCACCCAGCCCTTAAAGTGGTGGCCAGAATGCAGGAAGTGCTGTGGTTTGACTTTGTTTTTCCTGTAG
Seq C2 exon
CCAGGGCCCATACCTCCACCCCCAGAGAGATCGGGCTCAGGACCTGTGAGCAGCTGCTGCAGTGTTTCGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182472:ENST00000328867:15
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
NO
A:
NA
C2:
NO


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

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development