Special

HsaEX0066837 @ hg19

Exon Skipping

Gene
Description
TNF receptor-associated factor 5 [Source:HGNC Symbol;Acc:12035]
Coordinates
chr1:211499957-211529810:+
Coord C1 exon
chr1:211499957-211500231
Coord A exon
chr1:211527752-211527809
Coord C2 exon
chr1:211529709-211529810
Length
58 bp
Sequences
Splice sites
3' ss Seq
ATTTTAATTTTTTTCTCCAGAGA
3' ss Score
9.31
5' ss Seq
GAGGTAAGA
5' ss Score
10.06
Exon sequences
Seq C1 exon
AGACGCACGTGAGGGAAATCAGATGACTGGACTTGTAGATACTAACGGTTCTGAAGCGGGTAGGTTAGCTTTCCAACCGCCTGGATGACGGTCTCAGCCTCCTCCCGACCCCTTCCTGCGCGTCCGCTCTTCCCCTGCGCCCGCCCGCGCCCCTCCGCCCGCGCCCCGGCCCCGCCCCAGGCCTCGCCTCCGCTTCGCCGCCGCCGCCGGCCGCAGCCAGGAGCAGCAGCCGCGCCTGCAGACCGGCCTCGCGGAGCCCGCGCGCCGAGCCCCAC
Seq A exon
AGAATTAAACACAGTGCCAATCTGCCCTGTAGATAAAGAGGTCATCAAATCTCAGGAG
Seq C2 exon
GTTTTTAAAGACAATTGTTGCAAAAGAGAAGTCCTCAACTTATATGTATATTGCAGCAATGCTCCTGGATGTAATGCCAAGGTTATTCTGGGCCGGTACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000082512_MULTIEX1-3/11=C1-4
Average complexity
C3
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

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

C1:
NA
A:
PF0009720=zf-C3HC4=PD(25.6=50.0)
C2:
PF059116=DUF869=PU(4.5=26.5),PF086146=ATG16=PU(13.9=32.4)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CGTCCGCTCTTCCCCTGC
R:
ACTTCTCTTTTGCAACAATTGTCT
Band lengths:
187-245
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development