Special

HsaINT0027389 @ hg38

Intron Retention

Gene
ENSG00000182472 | CAPN12
Description
calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]
Coordinates
chr19:38738273-38738503:-
Coord C1 exon
chr19:38738418-38738503
Coord A exon
chr19:38738348-38738417
Coord C2 exon
chr19:38738273-38738347
Length
70 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGA
5' ss Score
6.71
3' ss Seq
TCACACCACAGTCTCTCCAGCTG
3' ss Score
0.71
Exon sequences
Seq C1 exon
GTGTTCCTGGGCTTCACCAAGGTGCGGCTGCTGCGGCTGCGGAACCCATGGGGCTGCGTGGAGTGGACGGGGGCCTGGAGCGACAG
Seq A exon
GTGGGATGGGTCTGGGGTGGGTGTGGGGCTGGACCCCACCTGCCCGCCCCTCACACCACAGTCTCTCCAG
Seq C2 exon
CTGCCCACGCTGGGACACACTCCCCACCGAGTGCCGCGATGCCCTGCTGGTGAAAAAGGAGGATGGCGAGTTCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182472:ENST00000328867:7
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:
PF0064816=Peptidase_C2=FE(13.7=100)
A:
NA
C2:
PF0064816=Peptidase_C2=FE(12.3=100)


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:
GTGTTCCTGGGCTTCACCAAG
R:
CAGAACTCGCCATCCTCCTTT
Band lengths:
161-231
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