Special

HsaINT0027500 @ hg38

Intron Retention

Gene
Description
calpain 5 [Source:HGNC Symbol;Acc:HGNC:1482]
Coordinates
chr11:77119030-77120909:+
Coord C1 exon
chr11:77119030-77119152
Coord A exon
chr11:77119153-77120712
Coord C2 exon
chr11:77120713-77120909
Length
1560 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGG
5' ss Score
9.16
3' ss Seq
GCCCCTCCCGCCTCCTGCAGGTG
3' ss Score
12.5
Exon sequences
Seq C1 exon
TACATCTTCGAAGTCAAGAAGCCAGAAGATGAAGTCCTGATCTGCATCCAGCAGCGGCCAAAGCGGTCTACGCGCCGGGAGGGCAAGGGTGAGAACCTGGCCATTGGCTTTGACATCTACAAG
Seq A exon
GTGAGGCCAGCCGGGTCCCCTGCCGTGGGTGGGGAGAGGGAGGGAGCTGGAGTTTGGACTGCCCATGCCTGAGGAAGAACGCTCTAGAACACCTTGGTCACTGCCGCTGCCCTGGCTGCCGTGGCAGACATTGTGAGGATGCCGTGGCATGGGCCCCACTTGAATATTCACAGAGGGCCCAGCCTGCCCAGCCTTGGCTTCTGTGGGAGCTCTCAGCCTGATTTCTTTCTGCCTAAGACCCACAGGCCTGGGATGTTTGGTGGATGAGGAAGGGGAAGATTACTGGTGGTTGGGGCCGGGCCCTGGGAGGCTCTGGGCATCTACTGGGCCCCCACTGCTCCTCCCTCAGGCCTCAGGGCCCCTTGCAGCCCCTTAGCCTTCCTGCATTGGAGGCCTTGCTGGGCACCAGGAGGAGGCATCCTTGAGCATAGCCAGGTGGGGTCACCTATGGCCGCACCGCCTGGCCTGGAACCTGAGGCCTTCCACGTGTTGTGATGCCCAGTGTGTGGTGACAGTCAGCATGGCGGGACCCCATGTGCCTGTCAGACCTTGAGAACGGAATGAAGCCACCGGGCCCTGCAGAGGCTGGGTACATGCTGAGTCCTTGGCATCTGATGTGCCTGGCCACGCCGTGGCACTTTGTTTATACTCTTGTGCTGGTACATTCATTGCATGCTAGTGTCTTGTGACATATTGTTGTGACTTTGCCATGTGACGATCTTCACTAGTGTGACCAGAACACTTTTTTCAGGATTGTCAGGCAGGTCCTGGCAGCTGGTGATGGCATTTCGTGGACAGGTGCTGTGACCTCTGCAGATCCTGATACTTGGTTGTGCTGTTGGAGTCAGAAACCCCACTGACATTGTTACCAGGGGGATTCCTATTGCCCTCTATTTTTTTTGTTTGTTTGTTTTACAGAGGGTCTTGCTCTGTAACCCAGACCAGAGGGCAGTGGTGCTGTCATAGCTCATTACAGTCTCAAACTCCTGGACTCAAACGATCCTCCCACCTCAGTCTCCCTAGTAGTTGGGACTATAGGTGAACACCACCATGCCTGGCTAATTTTTAAGTTTTTTGTAGAGCTGGGGTCTCGCTTTGTTGCCCATGCTGACCTTGAACGTCCAGCTTCAAGTGTTCCTCCCACCTTGGCCTCCCAAAGCGCTGGGATTACAGGCATGAGCCACTGCGCCCAGCCTCCTTTAATAGTTTTTATTGAGATATAATTCACAGAGCATGCAATTCAGCCATGTAAAGTATACAATCTAATGACTTTTGTGTGATCAGAGTTTATGCAACCATCACCACAATCAACTGTAGAACATTTTCATCTCCCCAAAAGAAACCCACTCCCTTTAACCACCACCACCCATTCCCATTGACCTCTTCCCTTCAGCCCTGGGCAAACACGAATCCGCTTCTGTTATTATAGATTTGCCTGTTCCGGACATTTCATATAAAGGGATTCCATCGTCCCTTCCATGGTGGTGAGGGGGAGGCGGGGTGGGCCAGGGTGTTGTAGGGTGTGTCTCCGCGTGGCCCAGCCCCTCCCGCCTCCTGCAG
Seq C2 exon
GTGGAGGAGAACCGCCAGTACCGCATGCACAGCCTGCAGCACAAGGCCGCCAGCTCCATCTACATCAACTCACGCAGCGTCTTCCTGCGCACCGACCAGCCCGAGGGCCGCTATGTCATCATCCCCACAACCTTCGAGCCAGGCCACACTGGCGAGTTCCTGCTCCGAGTCTTCACTGATGTGCCCTCCAACTGCCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000149260:ENST00000278559:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.083 A=NA C2=0.045
Domain overlap (PFAM):

C1:
PF0106717=Calpain_III=FE(27.8=100)
A:
NA
C2:
PF0106717=Calpain_III=FE(45.1=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:
ACATCTTCGAAGTCAAGAAGCCA
R:
GGCAGTTGGAGGGCACATC
Band lengths:
318-1878
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