Special

HsaEX6006260 @ hg38

Exon Skipping

Gene
ENSG00000184012 | TMPRSS2
Description
transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:HGNC:11876]
Coordinates
chr21:41471806-41476620:-
Coord C1 exon
chr21:41476577-41476620
Coord A exon
chr21:41473325-41473496
Coord C2 exon
chr21:41471806-41471981
Length
172 bp
Sequences
Splice sites
3' ss Seq
CTCCTGTTTGTCATCCTCAGCCT
3' ss Score
7.65
5' ss Seq
AAAGTATGC
5' ss Score
5.06
Exon sequences
Seq C1 exon
TGATGCCTGTTCTTCAAAAGCAGTGGTTTCTTTACGCTGTATAG
Seq A exon
CCTGCGGGGTCAACTTGAACTCAAGCCGCCAGAGCAGGATTGTGGGCGGCGAGAGCGCGCTCCCGGGGGCCTGGCCCTGGCAGGTCAGCCTGCACGTCCAGAACGTCCACGTGTGCGGAGGCTCCATCATCACCCCCGAGTGGATCGTGACAGCCGCCCACTGCGTGGAAAA
Seq C2 exon
ACCTCTTAACAATCCATGGCATTGGACGGCATTTGCGGGGATTTTGAGACAATCTTTCATGTTCTATGGAGCCGGATACCAAGTAGAAAAAGTGATTTCTCATCCAAATTATGACTCCAAGACCAAGAACAATGACATTGCGCTGATGAAGCTGCAGAAGCCTCTGACTTTCAACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000184012-'34-26,'34-24,36-26
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
PF154941=SRCR_2=FE(15.6=100)
A:
PF154941=SRCR_2=PD(5.2=8.6),PF0008921=Trypsin=PU(19.2=75.9)
C2:
PF0008921=Trypsin=FE(25.8=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATGCCTGTTCTTCAAAAGCAGTG
R:
CGTTGAAAGTCAGAGGCTTCT
Band lengths:
218-390
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains