Special

HsaEX6084609 @ hg19

Exon Skipping

Gene
ENSG00000185873 | TMPRSS11B
Description
transmembrane protease, serine 11B [Source:HGNC Symbol;Acc:25398]
Coordinates
chr4:69094975-69098134:-
Coord C1 exon
chr4:69098096-69098134
Coord A exon
chr4:69096921-69097098
Coord C2 exon
chr4:69094975-69095234
Length
178 bp
Sequences
Splice sites
3' ss Seq
TAAATAAATCCTTTCTCTAGGTT
3' ss Score
8.7
5' ss Seq
TAAGTAAGT
5' ss Score
8.07
Exon sequences
Seq C1 exon
AAATCAGCAAGGCTGCTTCTGAAATGCTTACCAACAACT
Seq A exon
GTTGTGGGAGACAAGTAGCCAACAGTATCATAACTGGCAACAAAATTGTGAATGGAAAAAGCTCCCTGGAGGGGGCATGGCCATGGCAGGCCAGCATGCAATGGAAAGGCCGTCACTACTGTGGAGCCTCTCTGATCAGCAGCAGGTGGCTATTATCTGCAGCTCACTGCTTTGCTAA
Seq C2 exon
GAAAAATAATTCAAAAGATTGGACTGTCAACTTTGGAATTGTAGTAAATAAACCATATATGACACGGAAAGTCCAAAACATTATTTTTCATGAAAATTATAGCAGTCCTGGGCTTCATGATGATATTGCCCTTGTGCAGCTTGCTGAAGAAGTTTCTTTTACAGAGTACATTCGTAAGATTTGTCTTCCTGAAGCCAAAATGAAGCTCTCAGAAAATGACAATGTTGTAGTTACAGGTTGGGGAACACTTTATATGAATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185873-'5-7,'5-5,7-7=AN
Average complexity
A_C1
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:
NO
A:
PF0008921=Trypsin=PU(19.5=73.3)
C2:
PF0008921=Trypsin=FE(38.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCAAGGCTGCTTCTGAAATGC
R:
AGAGCTTCATTTTGGCTTCAGGA
Band lengths:
242-420
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains