Special

HsaINT0027326 @ hg38

Intron Retention

Gene
Description
calpain 1 [Source:HGNC Symbol;Acc:HGNC:1476]
Coordinates
chr11:65209849-65210096:+
Coord C1 exon
chr11:65209849-65209917
Coord A exon
chr11:65209918-65210017
Coord C2 exon
chr11:65210018-65210096
Length
100 bp
Sequences
Splice sites
5' ss Seq
CTGGTAGGT
5' ss Score
8.37
3' ss Seq
ACCCTCTGCCGCCACCTCAGTCC
3' ss Score
3.54
Exon sequences
Seq C1 exon
CGTGATGGCAATGGGAAGCTGGGCCTGGTGGAGTTCAACATCCTGTGGAACCGCATCCGGAATTACCTG
Seq A exon
GTAGGTTGTCCCCACTCACCTCAGTCATGCAGGTGCGGGCCGGGCAGGTGGGAAGGGCCGGGTGACTCAGCCTGGCCCTCACCCTCTGCCGCCACCTCAG
Seq C2 exon
TCCATCTTCCGGAAGTTTGACCTGGACAAGTCGGGCAGCATGAGTGCCTACGAGATGCGGATGGCCATTGAGTCGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000014216:ENST00000533820:18
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=PD(29.5=78.3),PF134991=EF-hand_7=PU(5.5=21.7)
A:
NA
C2:
PF134991=EF-hand_7=FE(28.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGATGGCAATGGGAAGCTGG
R:
CTGCCGACTCAATGGCCATC
Band lengths:
147-247
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