Special

HsaINT0027382 @ hg38

Intron Retention

Gene
ENSG00000182472 | CAPN12
Description
calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]
Coordinates
chr19:38730965-38731223:-
Coord C1 exon
chr19:38731107-38731223
Coord A exon
chr19:38731024-38731106
Coord C2 exon
chr19:38730965-38731023
Length
83 bp
Sequences
Splice sites
5' ss Seq
TCTGTGAGT
5' ss Score
7
3' ss Seq
CCCTGCCCCTCTCTGCACAGGCC
3' ss Score
11.33
Exon sequences
Seq C1 exon
GCTTCCACCTGAACAACCAGCTGACCCAGACCCTCACCAGCCGCTACCGGGATAGCCGTCTGCGTGTGGACTTCGAGCGGTTCGTGTCCTGTGTGGCCCACCTCACCTGCATCTTCT
Seq A exon
GTGAGTACCACCCCGGCATGGTGGGGCATGGGGGGAAGGGGTACGGGGACTGGTGGGCACTCACCCTGCCCCTCTCTGCACAG
Seq C2 exon
GCCACTGCAGCCAGCACCTGGATGGGGGTGAGGGGGTCATCTGCCTGACCCACAGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182472:ENST00000328867:19
Average complexity
IR
Mappability confidence:
NA
Protein Impact

Alternative protein isoforms

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

C1:
PF134991=EF-hand_7=PD(46.3=77.5)
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:
TTCCACCTGAACAACCAGCTG
R:
GTCTGTGGGTCAGGCAGATGA
Band lengths:
172-255
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development