Special

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


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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