Special

HsaINT0027358 @ hg19

Intron Retention

Gene
ENSG00000137225 | CAPN11
Description
calpain 11 [Source:HGNC Symbol;Acc:1478]
Coordinates
chr6:44148485-44148734:+
Coord C1 exon
chr6:44148485-44148542
Coord A exon
chr6:44148543-44148669
Coord C2 exon
chr6:44148670-44148734
Length
127 bp
Sequences
Splice sites
5' ss Seq
AATGTGAGT
5' ss Score
7.8
3' ss Seq
ACCCCTTCCCTTCCTCACAGTCA
3' ss Score
10.9
Exon sequences
Seq C1 exon
GGCAAGGAGATAGGGGTGTATGAGCTCCAGAGGCTGCTCAACAGGATGGCCATCAAAT
Seq A exon
GTGAGTCTTCCACTCCTGCTGCACACGACCCCTCCCCCATATTTTGTGCCCCTCTTGATCACTCCCAGTGCCCCCACGATACCTCATTTACCCTGTCTCTCCTTTCTACCCCTTCCCTTCCTCACAG
Seq C2 exon
TCAAAAGCTTCAAGACCAAGGGCTTTGGCCTGGATGCTTGCCGCTGCATGATCAACCTCATGGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137225-CAPN11:NM_007058:17
Average complexity
IR-S
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:
PF138331=EF-hand_8=FE(31.1=100)
A:
NA
C2:
PF138331=EF-hand_8=FE(34.4=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:
GGCAAGGAGATAGGGGTGTATG
R:
ATGAGGTTGATCATGCAGCGG
Band lengths:
119-246
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