Special

HsaEX0066072 @ hg19

Exon Skipping

Gene
ENSG00000184012 | TMPRSS2
Description
transmembrane protease, serine 2 [Source:HGNC Symbol;Acc:11876]
Coordinates
chr21:42852403-42861520:-
Coord C1 exon
chr21:42861434-42861520
Coord A exon
chr21:42860321-42860440
Coord C2 exon
chr21:42852403-42852529
Length
120 bp
Sequences
Splice sites
3' ss Seq
TCTTCTGTTTTCTCTGCAAGTGG
3' ss Score
5.37
5' ss Seq
GTGGTGAGT
5' ss Score
8.95
Exon sequences
Seq C1 exon
AGACTAAGAAAGCACTGTGCATCACCTTGACCCTGGGGACCTTCCTCGTGGGAGCTGCGCTGGCCGCTGGCCTACTCTGGAAGTTCA
Seq A exon
TGGGCAGCAAGTGCTCCAACTCTGGGATAGAGTGCGACTCCTCAGGTACCTGCATCAACCCCTCTAACTGGTGTGATGGCGTGTCACACTGCCCCGGCGGGGAGGACGAGAATCGGTGTG
Seq C2 exon
TTCGCCTCTACGGACCAAACTTCATCCTTCAGGTGTACTCATCTCAGAGGAAGTCCTGGCACCCTGTGTGCCAAGACGACTGGAACGAGAACTACGGGCGGGCGGCCTGCAGGGACATGGGCTATAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000184012_CASSETTE2
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

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

C1:
PF126692=P12=PU(21.4=70.0)
A:
PF126692=P12=FE(40.8=100),PF0005713=Ldl_recept_a=WD(100=92.7)
C2:
PF126692=P12=PD(36.7=83.7),PF154941=SRCR_2=PU(39.6=88.4)


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCACTGTGCATCACCTTGACC
R:
TATAGCCCATGTCCCTGCAGG
Band lengths:
202-322
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