Special

HsaINT0027366 @ hg38

Intron Retention

Gene
ENSG00000137225 | CAPN11
Description
calpain 11 [Source:HGNC Symbol;Acc:HGNC:1478]
Coordinates
chr6:44169906-44172420:+
Coord C1 exon
chr6:44169906-44169975
Coord A exon
chr6:44169976-44172301
Coord C2 exon
chr6:44172302-44172420
Length
2326 bp
Sequences
Splice sites
5' ss Seq
TCGGTGAGT
5' ss Score
11.11
3' ss Seq
AGCCCTGCCTGTCTTTCCAGGGG
3' ss Score
9.7
Exon sequences
Seq C1 exon
GATATCATAAACAACCCTCTATTCATCATGGATGGGATTTCTCCAACAGACATCTGCCAGGGGATCCTCG
Seq A exon
GTGAGTGGGGCACAGGAAGCTGGTCTCCACCTGGGCAAGAGGATTGGGGGAGGGGTGCCAGGGTGTCTTTTGAAGCTGGGAAACAGGGAGCCCTGAGGTCAGACAGCCTGCTTCTGTTCCCCTGTCCCTCCCCTTCTGAGGAGATGACAGTGAGAACACCGTGCATTCTTCCTGCCCCTCCCAAGTCTGGATGCCACTCCCTGCCTGCTGCAGCCTGGGTCTTGCGGGGGGAATATTAGTTACATTTGACTACATAATAAATTACCTAGGACTTAGCAACTTAAAAAAAAAATTTCTTATCTCACGGTTCCTGTGGGTCAGAAATTCAGAAGCAGAATCACTGGATGGGTCTAGTTCAGGGTTTATCAGGAGGTTACAGTCAAGACGTCTGCAACCTGTGATCATCTGAAGGCTCGCCTGGGGCTGGAGGGTCTGCTCCTAGGAGGGTGCACTTACGTGGCAGGAGCTCTCAGGTCTTTGCTGGCTGTTGGCAGGAGGCCCCAGTTCCTCACCACATAGGCTTCTCCATGGGGCTGCTTGAGTGTCCACGCAACGTGGTAGCTTGCTCTTCCAAAGCGAGTTATCTAAGAGAGAGGACAAGGAGGAAGCCATAATGCCTTTTCTGACCTAGTCTCAGGAGTTGCACATCATCACTTCCACCATATTCTATTTGTTAGAAGCAAGCACTGAATCTGGTCCACACTCAAGAGGAGAGGAATTAGGCTCTACCTTTGGAAGGGAGGATGGTCAAAGAATTTGTAGAAACCACTACAGGTGCTAGAACCCGATCAATCTGGGGTATCAAATAGGAGGGCAACGGGGTCTACTCAGCCCACTCTCACAGGGCTCCCATAGAAAGCCCCAGGGTAGATCTTTCTCCCTAAGTCTGGTCCCGTTCAAGGGTTTCTTCCAGATCCCTCGCTGCCTCTTTAGGGATAAAGCCAGGGTGGGCTTTCTCTGAGACTGAATTCTGTCCCCTTGGGGCAGAAAAAAGGGCAAGGTGTGGGCAGAGCAGAGGCCAAGGAGACCTTAGACCCCAGGGCCGCTGCTGTGGCCGCTGTGGCTCAGTAGGCTGGAGGGACAATGGGCTGGAGGAGGGAATTCACTTCTCCGAGGCACTCTAACAGTGAGGGGGATTGGAGCGCCCTTGATATTCCTCTCTCCAGGCAGCCAAGAGGCCATTGGTAATCATAGAAACTTTCTGCTCCCTCAACCTCAGCCTGGCGTAGGATGCACAGCACCCTGCCCCTGGACCCCACCCAGCAAGGGCTGAGATGCCTAGGAGACAGGTGGCAATGGAGGTCTGTAGTGCTCATCTCCCATAGGATTCCCTTTAGCCGAACTTCAGGCCAGGGACACTGCCTCATACCCACTTCAATGCCTAGCTCCAGGGACCCTGCTGGGGCACATACTGAGCCCTGGGTCCCCAATATAATGTGGGTGACATGAGGGAGAGACCTCTTGGGAACTTCGTGGCCACACCAGTGTACTCACAGGGTGCAGGAAGGTGACTGGATCTGTTGGAAGAATGTGGAGAGTATTGGCTCTGTCTCAAAGAAAGCAGGTTACTGGTCAGGTGCAGTGGCTCATACCTGTAATCCTAGCACCTTGGGAGGCCAAGGCAGGAGGACTGCTTGAGCTCAGGAGTTCAAGACCAGCCTAGGCAGCATAGTGAGACTCTGTCTCTACTTATATATAAAAATTTACTTTAAAAAAAAATAGGTTCCTAGAGCCTGAGGCCAAAAGTACCTCTTTTCCAAACTCAAGAAAAACAAAAGGATGTGTCTCTCACATAATAGAAAAGGTACAGCCAGGCACTGTGGCTCACACCTGTAATCCCAACACTTTGGGAGGCCAAGGCTGGCAGATCTCTTGAGGCCAGGAGTTTAAGACCAGCGTGGCCAACATGGTGAAACCCCATCTCTACTAAATATGCAAAAATTAGCCAGGTGGGGTGGCGGGCGCCTGTGGTCCCAGCTACTCAGGAGGCTGAGACAGGAGAATCGCTCGAACCCAGGAGGCAGAGGTTGCGGTGAGCTGAGATCATGCTATTGCACTCCAGCCTGGGTGACACAGCAAGACACTGACTCAAAAAAGAAAATGTACAGAAACTCACCTTACTAGAGTCTCTCCGCCTTCAGTTTCTCCCTGTTTACCTCCTTCCTGAACACTCTTTAGTGGGAGGGCTGAGGGAGGGTGCCTCTCCGCCGGGGGGGTGAGAATGGGGTACAGGGTCAAGTTCCTGCTCCCCTAGGCCTTGGATTCTGAGGCCCACCCACACATATGGGGTTGCTCAGGGGTGGCAAAGCCCTGCCTGTCTTTCCAG
Seq C2 exon
GGGACTGCTGGCTGCTGGCTGCCATCGGCTCCCTTACCACCTGCCCCAAACTGCTATACCGCGTGGTGCCCAGAGGACAGAGCTTCAAGAAAAACTATGCTGGCATCTTCCATTTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137225:ENST00000398776:4
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:
PF0064816=Peptidase_C2=FE(31.1=100)
A:
NA
C2:
PF0064816=Peptidase_C2=PD(20.3=88.2)


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

  • Autistic and control brains
  • Pre-implantation embryo development