Special

HsaEX1029707 @ hg38

Exon Skipping

Gene
ENSG00000172460 | PRSS30P
Description
protease, serine, 30 pseudogene [Source:HGNC Symbol;Acc:HGNC:28753]
Coordinates
chr16:2839568-2841848:-
Coord C1 exon
chr16:2841680-2841848
Coord A exon
chr16:2841163-2841328
Coord C2 exon
chr16:2839568-2839931
Length
166 bp
Sequences
Splice sites
3' ss Seq
ACCCGCCCATCCCTCTGCAGAAT
3' ss Score
11.53
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
Exon sequences
Seq C1 exon
CACAGAGGGCTCCAGCGTGATTGCCACTGGTTAATGACCTGCCACCCCCGCCCCCCCAACCTCTGGTGCCGTCCAAGGACTCTGACCCCAGTGCAGTGTCTGTAGGGAAGAGGAGCCATGGGGCTTCGGGCAGGCCCCATCCTGCTTCTGCTGCTGTGGCTGCTGCCAG
Seq A exon
AATGCGGCCACTCCAAGGAGGCCGGGAGGATTGTGGGAGGCCAAGACACCCAGGAAGGACGCTGGCCGTGGCAGGTTGGCCTGTGGTTGACCTCAGTGGGGCATGTATGTGGGGGCTCCCTCATCCACCCACGCTGGGTGCTCACAGCCGCCCACTGCTTCCTGAG
Seq C2 exon
GGTGACTCCGGGGGGCCGCTGGTCTGCCCCATCAATGATACGTGGATCCAGGCCGGCATTGTGAGCTGGGGATTCGGCTGTGCCCGGCCTTTCCGGCCTGGTGTCTACACCCAGGTGCTAAGCTACACAGACTGGATTCAGAGAACCCTGGCTGAATCTCACTCAGGCATGTCTGGGGCCCGCCCAGGTGCCCCAGGATCCCACTCAGGCACCTCCAGATCCCACCCAGTGCTGCTGCTTGAGCTGTTGACCGTATGCTTGCTTGGGTCCCTGTGAACCATGAGCCATGGAGTCCGGGATCCCCTTTCTGGTAGGATTGATGGAATCTAATAATAAAAACTGTAGGTTTTTTATGTGTATTTTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000172460-'4-7,'4-4,7-7
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

NonCoding

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

C1:
NA
A:
NA
C2:
NA


Main Inclusion Isoform:
NA


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Primers PCR
Suggestions for RT-PCR validation
F:
TGTAGGGAAGAGGAGCCATGG
R:
CCCAGACATGCCTGAGTGAGA
Band lengths:
246-412
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains