Special

HsaINT0027434 @ hg19

Intron Retention

Gene
ENSG00000214711 | CAPN14
Description
calpain 14 [Source:HGNC Symbol;Acc:16664]
Coordinates
chr2:31415997-31417349:-
Coord C1 exon
chr2:31417275-31417349
Coord A exon
chr2:31416161-31417274
Coord C2 exon
chr2:31415997-31416160
Length
1114 bp
Sequences
Splice sites
5' ss Seq
CTGGTATTG
5' ss Score
3.14
3' ss Seq
TTTCCTTCTTCTCTCCACAGGAT
3' ss Score
14.53
Exon sequences
Seq C1 exon
TTCAAGTAAATGGGAGCTGCTGAGCCCCAAGGAGAAGATTCTGCTTCTGAGGAAAGACAATGACGGAGAATTCTG
Seq A exon
GTATTGGACTTAGGGACTTGGACAAATGTCCTGGCCTACATTTGAAAACCCATCCAGCAGACATTTATTGGATGCCTTATGGGTGCCAGGAACTTCATGTACAGAGATCAATAAGGCACCATCCCTTTAGGAGCTCACGGTCTAGCAGGACAAACAGTGCCTGTAAATAAACGGTCACTGTCTTTGTGATGAGAGTAGAGGCCACTAGGGTGGAGCTCAGCGAGGGCTCAGCCAGGCTGTTTCCTCCTCTCTGGCTTCCTCTCTGCTCTCTTGCTCAGTGTATTCAAAACAGGTTTTGCCTTTTTTGTCCTGAAAAGGCCATGAGGTAGGAAGAGACTGCAAAGTCTTGTCATAGGATAGGCCCCTGACCAGTGCCCTCCAGAGCAGAGTAACACTGCCACCCACTCTGGGGCTGCTCACCTCATTTTTTGAAAGGCCACCAAGACATCCTGAGCTGATGCTGCTTCTAGGTGTCTGAAATGGACCCATCAGTTCTCCTTTGCTTTTGCTCACCACCGTTACTGTGAATGTCAACCCTCGTTCCAAGGACTGCTCCCATTAACCATCCAGTACAGCCTGCCACCGCCCTCTCCCTTTGGAAGGTCTTTCACTGAACTCAAGCTCTGCAAATTCCTGTTTTTTCCACTTTATGGTTAAGTAAACTGAGCATCAGACAGCTTAAATAGAGTGTCGCAGGCCACAAGTTAGCAAGTAGGGGCAAAGATCTTCATGAATTAATGATTAAGAACTGATATGTAATTCTTATTGAACATTTATAGATAAAACAAATGACTAGTTAGCTATGCCTTAATTCAGCTGCTATCACCATGATTCCAGAAACTGGAACATCTCCCCCGGTCAGCCATGTGGCCGGCTGCTTCCAGCCAGAGGGTGGGGCTTCTCAGTAGCTCCAGCCCCCCACGATGGACCCTCACAGGGATCTAGCCAGCCCCAGCTGATGTGCCTATCGTCAGCTCAGCTCTGCACAAGAGCTGGTGTCTTTGTCCATGAGAGGGCTGGGATGCCCACTGCTCCGTTTCACCCTCCCCATGGGTCCTGATAACTAGGCGTTATCTGGTCCATCTCTTTGTGCTTTTCCTTCTTCTCTCCACAG
Seq C2 exon
GATGACGCTGCAGGACTTTAAAACACATTTCGTGCTCCTGGTTATCTGTAAACTGACCCCAGGCCTGTTGAGCCAGGAGGCGGCCCAGAAGTGGACGTACACCATGCGGGAGGGGAGATGGGAGAAGCGGAGCACAGCTGGTGGCCAGAGGCAGTTGCTGCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000214711-CAPN14:NM_001145122:9
Average complexity
IR-S
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(8.5=100)
A:
NA
C2:
PF0064816=Peptidase_C2=PD(6.5=33.9),PF0106717=Calpain_III=PU(16.4=44.6)


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:
TCAAGTAAATGGGAGCTGCTGA
R:
CTGGCCACCAGCTGTGCT
Band lengths:
222-1336
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