Special

HsaINT0027441 @ hg38

Intron Retention

Gene
Description
calpain 2 [Source:HGNC Symbol;Acc:HGNC:1479]
Coordinates
chr1:223764150-223766431:+
Coord C1 exon
chr1:223764150-223764207
Coord A exon
chr1:223764208-223766366
Coord C2 exon
chr1:223766367-223766431
Length
2159 bp
Sequences
Splice sites
5' ss Seq
AGCGTGAGT
5' ss Score
8.2
3' ss Seq
ACACTGATTTTGTCTTTTAGGCC
3' ss Score
10.85
Exon sequences
Seq C1 exon
GATGCGGAGATCTCTGCCTTTGAGCTGCAGACCATCCTGAGAAGGGTTCTAGCAAAGC
Seq A exon
GTGAGTATCCCCTCATTGCAAAACCTCATCCTGCTCTTTCCCCTGTGGATGGGAGGGAACATGGAAATCTTTCCCCCTCCATGTCTGGCTGCTGTGACTAAACCACCACCCTCCATCCCCTCCAAGAAGTGGATGAAGGATTTGTATGATGTGATGAAAAAGAACAAGTGTTTGTAGCATCCACAGATCAAAGATCAAATCCAGGTTTCCACTACATACTAGCTTTGTGTGATCTATTTTTTTAATTTATTTTATTTTATTTTTGAGACAGAGTCTCACTCTGTCGCCCAGGCTGGAGTAAAGTGGCACAATCTCAGCTCACTGCAATCTCTACCTCCCAAATTCAAGCGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGAATCACAGGCAAGTGCCACCACAGCCAGCTGACTTTTGTATTTTTAGTAAAGACAGGGTTTCACCATATTGGCCAGGCTGGTCTTGAACTCCTGACCTCAAGTGATCCACCTGCCTTGGCCTCCCAAAATGCTGGGATTACAGGCATGCACTACCACATCCAGCTAATTTTTGTATTTTCCTAGAGATGGGGTTTCTCCATGTTGGCCAGGCTGGTCTTGAACCCCTGGCCTCAAGTGATCTGCCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCGTGCCCGGCCACATCTTGTAACTAACTATTTCTTAAGCAAAAAAATGTCAGAGGATTGATTGTTCAACCCCTTACTGTGGATCACCAGCAGGGAGGAGCGGGAAACACAACACAGAGACATTTTTTCCCCTCAAATTATCAAAAGAATCACGCTGCATTTGTTAAGAGAGCAACTGGCAATCCAGGAAGCAGAGTTTTGAACATATCAGAAGTTAGGAATCTGCATCAGAGACAAATGCAGTCATGGTTGTTTGCTGCATACCAGCCCTAGGGATCATCTCGAGAAGCCTCATGGACTTCAAGGGACATCATTCCCTCTGACAAGATGGCCTCTAGCCTAACTCCATGAGATAAAATAAATCTGCCTTTCAGAGCCAAAGAAGAGTCCAGGGCCAGCTGGGTCTTCCCTCCCAGTGTGAACCAAGAGGGCTGGGCCAGTCAGGTTACGGTCAGTCCAGTGCAGGGCCTCCCCAGAGGAGACCCAGTCTGCACCCGCCCTCCTCTAATTTTCAGGGAAGGCAAGAAGATTGTGTTTACCCTGGAGGCCACCAGGCACAAGTGAGGTCACAGAGCTCTTCAGATATGCAGTCCTCATGAGCTGAGGAGACTAAAGCCTCATTGTTTCTGCACAGATGGAGGGTGGGGCTGGGAGGTGGGGAAGAAGCGGGCCTTGCCTGGATTCAGCCCGCTCCTTGCTGGGGGAGCAGCATTCGCTCCGCGCGTGCCTCTGAGCTTACTACCCTACCCCTAGCTGCCTGCTGACTCCAGCCTTCTGGAGGGCTCCACACCAGAGTCTGCATGCACAGCTGCTGGGCCAGAGCCTTATGACCATCTAAGGGGTTGGTGCCCAGAGTGGCAGCTTTGAGGCAGGTCAGGCTCTAACCTCTTTCGGGGACATAACAAAAAGGCTGGGCTTTTCGTGAAGTCTGTGGGGAGCCAGGTTCACATTGGTGACTAGGGAGGGTCTCATGCCACCTGCCAAACACCAAGTGGACAGGACTCACTTAGTGCAGCACAAATAGCTCGTGGATCGATCCCAGTTCCTCAGGTTTCTCAGTCAGCTGGGGACACAGTCCATAAATGTCTGCAGATGGACAGTTCAAGTAAACCTCTTTCTCTCACGGGTCATAGCCTAGAATTAACACACCTGCTCTCTGTTTTCTTTTTCCCTGCCCAACAACTACAGGTGACTTTATATCCTGTGGGCACCTAAGGCCCAACCATTGATCATTCTGTTATTTATTTGTTCAAAAAGCACTTTTTAAAGCCCTGTTTGCCCACGGCAAATATACAGAGACATCAGGACAATGTGGACATCATCTGCACTGTCCCAGTCTGGTAGTCACTAGCCACATGTGGCTATTTAATATAATGGAAGTGGCTTCTGTATGTGAAGGGCACAGATAAAGAATATCTCCATGATTGTGGAAAGTTCAGTTGGACATCACCGCTCAGAGATTTTTCCTGTCACACTGATTTTGTCTTTTAG
Seq C2 exon
GCCAAGATATCAAGTCAGATGGCTTCAGCATCGAGACATGCAAAATTATGGTTGACATGCTAGAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162909:ENST00000295006:15
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:
Associated events
Other assemblies
Conservation
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