HsaINT0027363 @ hg19
Intron Retention
Gene
ENSG00000137225 | CAPN11
Description
calpain 11 [Source:HGNC Symbol;Acc:1478]
Coordinates
chr6:44150856-44151500:+
Coord C1 exon
chr6:44150856-44150972
Coord A exon
chr6:44150973-44151441
Coord C2 exon
chr6:44151442-44151500
Length
469 bp
Sequences
Splice sites
5' ss Seq
TCAGTGAGT
5' ss Score
7.68
3' ss Seq
CCGCTTCCTCTGTAACGCAGCAT
3' ss Score
4.69
Exon sequences
Seq C1 exon
GCATCAAGCTGAACAACAAGGTAATGCAGGTCCTGGTGGCCAGGTATGCAGATGATGACCTGATCATAGACTTTGACAGCTTCATCAGCTGTTTCCTGAGGCTAAAGACCATGTTCA
Seq A exon
GTGAGTTAGGCATCTACCCACTCCCCAGCCTAGGCCAGGGGCCGCGGGCCCTTTCCCAAACACCCACCCTGATGGGTGCTGCTCCAGATCCCCTCCCCCTTACAAGGCACACATGAAATGGATTCAAAGCCCAGCTCCGCCACTTGCTGGCAGAGGTGACTTGAGCAAGTCACTTAATCTTTCTGTGCCTCCATTCCCTCCTCTTTAGAATGTGGATAATAATAGTACTGCCCTCAAAGGACTGAGGTGCAGGTTAAACCAGTTAGTCTATGGAAGGCAATCAGAACTGGGCCTGGCTCCTGGTGAGGCTATGTGAGTTGCTATCATTAATTCCCCACTTGGCTAGGGGATTTATGTGGGGAACAGCCAGGAACACCTGGTGTCGCCCCTTCCTACCTAGTTGGGAGTGGTTCTTTCGGAACACTGACTTAGCATTCAGCCCCTCTCCCCCGCTTCCTCTGTAACGCAG
Seq C2 exon
CATTCTTTCTAACCATGGACCCCAAGAATACTGGCCATATTTGCTTGAGCCTGGAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137225-CAPN11:NM_007058:21
Average complexity
IR-C
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:
PF134991=EF-hand_7=FE(41.1=100)
A:
NA
C2:
PF134991=EF-hand_7=FE(20.0=100)
Main Inclusion Isoform:
NA

Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)