Special

HsaEX0017913 @ hg38

Exon Skipping

Gene
Description
chymotrypsin C [Source:HGNC Symbol;Acc:HGNC:2523]
Coordinates
chr1:15440300-15442572:+
Coord C1 exon
chr1:15440300-15440391
Coord A exon
chr1:15440493-15440590
Coord C2 exon
chr1:15442447-15442572
Length
98 bp
Sequences
Splice sites
3' ss Seq
CCCTCCCCACCCTCCTGCAGATC
3' ss Score
11.5
5' ss Seq
CAGGTGTGC
5' ss Score
6.46
Exon sequences
Seq C1 exon
CCTCCAGCTGTGGGGTGCCCAGCTTCCCGCCCAACCTATCCGCCCGAGTGGTGGGAGGAGAGGATGCCCGGCCCCACAGCTGGCCCTGGCAG
Seq A exon
ATCTCCCTCCAGTACCTCAAGAACGACACGTGGAGGCATACGTGTGGCGGGACTTTGATTGCTAGCAACTTCGTCCTCACTGCCGCCCACTGCATCAG
Seq C2 exon
CAACACCCGGACCTACCGTGTGGCCGTGGGAAAGAACAACCTGGAGGTGGAAGACGAAGAAGGATCCCTGTTTGTGGGTGTGGACACCATCCACGTCCACAAGAGATGGAATGCCCTCCTGTTGCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162438-'3-7,'3-6,4-7
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.286 A=0.019 C2=0.000
Domain overlap (PFAM):

C1:
PF0008921=Trypsin=PU(6.0=45.2)
A:
PF0008921=Trypsin=FE(13.7=100)
C2:
PF0008921=Trypsin=FE(18.0=100)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GAGTGGTGGGAGGAGAGGATG
R:
ACAGGAGGGCATTCCATCTCT
Band lengths:
169-267
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