Special

HsaINT1010333 @ hg38

Intron Retention

Gene
Description
chymotrypsin C [Source:HGNC Symbol;Acc:HGNC:2523]
Coordinates
chr1:15440300-15440590:+
Coord C1 exon
chr1:15440300-15440391
Coord A exon
chr1:15440392-15440492
Coord C2 exon
chr1:15440493-15440590
Length
101 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGC
5' ss Score
9.88
3' ss Seq
CCCTCCCCACCCTCCTGCAGATC
3' ss Score
11.5
Exon sequences
Seq C1 exon
CCTCCAGCTGTGGGGTGCCCAGCTTCCCGCCCAACCTATCCGCCCGAGTGGTGGGAGGAGAGGATGCCCGGCCCCACAGCTGGCCCTGGCAG
Seq A exon
GTAAGCCTGTGTAGGGCTGGGAGGTACAGATAGAGAGGGTGGCGGGGTGAGGGTCCCAGGGACCTGCAGGCTGACACACAGCCCTCCCCACCCTCCTGCAG
Seq C2 exon
ATCTCCCTCCAGTACCTCAAGAACGACACGTGGAGGCATACGTGTGGCGGGACTTTGATTGCTAGCAACTTCGTCCTCACTGCCGCCCACTGCATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162438:ENST00000375949:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.286 A=NA C2=0.019
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=PU(6.0=45.2)
A:
NA
C2:
PF0008921=Trypsin=FE(13.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
CCTCCAGCTGTGGGGTGC
R:
GCGGCAGTGAGGACGAAG
Band lengths:
178-279
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains