Special

HsaINT0027387 @ hg38

Intron Retention

Gene
ENSG00000182472 | CAPN12
Description
calpain 12 [Source:HGNC Symbol;Acc:HGNC:13249]
Coordinates
chr19:38738574-38740219:-
Coord C1 exon
chr19:38740051-38740219
Coord A exon
chr19:38738649-38740050
Coord C2 exon
chr19:38738574-38738648
Length
1402 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGA
5' ss Score
9.45
3' ss Seq
CCATCCCATCCCCTGCCCAGAGT
3' ss Score
5.49
Exon sequences
Seq C1 exon
GCTCCACGGCTCCTATGAGGTGATGCGGGGCGGCCACATGAATGAGGCTTTTGTGGATTTCACAGGCGGCGTGGGCGAGGTGCTCTATCTGAGACAAAACAGCATGGGGCTGTTCTCTGCCCTGCGCCATGCCCTGGCCAAGGAGTCCCTCGTGGGCGCCACTGCCCTG
Seq A exon
GTAAGAGACCTGGACTCGCATGCGGAACCCCCACCAGGACCAGAGCACAGTCAGGGGTGTGGTGGGGTGGGCGGAGTGCTTCCTCTGTTCTCTGCTTCCGTTACTGGCTTAGGCTCGCTCATAAATCTAACTAGTCAAAAATAAATTCATTTGCTCTCATGAATCAGGGGCTTCAGGCACAGCTGGATCCAGATGCTGAGGGTGTTGCAACTATGTTTATTTCTCATTCTGTGTTAGTGTCACTCTCAGCCAGGCTCTCCCCTCATGGGCATAAAAGGATCCCCCATAGCTGCAGGTATCTCCTACCACCCTAGGGTTTATTTAAAAAAAAAAAAAAAAAGTGCCTCTTTCTGAGAATTTCAGTAAAAGTCCCAGGATTGATTCTCGTGGGCTTAGCTTGGGTCATGTGTTCATCTGTGACCCCATGACACACTCATTCATTCACTGAGTTGGTCTAACTCCTTCACTCATTCATTTACTTAAATCCTCTGAGTTACTGCTTCTCTTTTTCTTTTGTGTCTGTTTCTCTCTTCTGTATCTTTCTTTGTCTCTGTCTCTGTCTCTCTACTCTTTCCATCTTTTTTTTTTTTTTTTTTTTTTTTGAGACGGAATCTTGCTCTGTCACCCAGGCTGGAGTGCAGTGGCACGACCTTGGCTCACTGTAACCTCTGTCACCCAAGTTCAAGCAATTCTCCTGCTTTGCCTCCCGAGTAGCTGGGACTACAGGCGCCCGCCACCATGCCCAGCTAGTTTTTTGTATTTTTAGTAGAGATGGGGTTTCACTGTGTTAGCCAGGATGGTCTCAATCTCCTGACCTTGTGATCTGCCCGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCACAACAGGCCTCTTTCCATCTATTTTGTTTGTTTTTGTTTTTGGAGGCAGGGTCTCATCTCACTCTGTCACCCAGGCCAGAGTGCAGTAGTGTCATCATAGCTCACTATAGCCTTGACCTCTGGGCTCAAGGGATCCTCCTGCCTCAGCCTCCAGAGTAGCTGGGACCACTGGTGTGCACCACCACGCCTGTTGAATTTTTAAAATTTTTGTAGACTTGGGGTCTTGCTATGTTGCCCAGGCTGGTCTTGGACTCCTGGCCTCAAGTAGTCCTTCCACCTCGACCTCCCTAAGTGCTGGGATTACAGGCGTGAGCCCGTACCTCCATCTCCTTTTGTCTCGTTTCCATCTCCCTTCCTCTCCTTTTCTCTTTCGCCTTCAGTCACTAACCCTGACATGGTCTCTGAGCTGCGTGCCATTCAGTTCAGTGCTCTGGTTGGCTCCTGCCTTGGTGGCAGGAGGTTGGGGGCAGGGAGGAGCAGCTGCCCTCCTGTCCCCTACCTTGGCCTCACCATCCCATCCCCTGCCCAG
Seq C2 exon
AGTGATCGGGGTGAGTACCGCACAGAAGAGGGCCTGGTAAAGGGACACGCGTATTCCATCACGGGCACACACAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000182472:ENST00000328867:5
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(18.9=100)
A:
NA
C2:
PF0064816=Peptidase_C2=FE(11.8=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:
CCACGGCTCCTATGAGGTGAT
R:
GTGTGTGCCCGTGATGGAATA
Band lengths:
238-1640
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