Special

HsaINT0027358 @ hg38

Intron Retention

Gene
ENSG00000137225 | CAPN11
Description
calpain 11 [Source:HGNC Symbol;Acc:HGNC:1478]
Coordinates
chr6:44180748-44180997:+
Coord C1 exon
chr6:44180748-44180805
Coord A exon
chr6:44180806-44180932
Coord C2 exon
chr6:44180933-44180997
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:ENST00000398776:17
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:
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:
NA
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