Special

HsaEX0055020 @ hg19

Exon Skipping

Gene
ENSG00000177359 | RP11-551L14.1
Description
NA
Coordinates
chr12:31285179-31286931:-
Coord C1 exon
chr12:31286813-31286931
Coord A exon
chr12:31286051-31286102
Coord C2 exon
chr12:31285179-31285262
Length
52 bp
Sequences
Splice sites
3' ss Seq
TTTGTGTTATTCTTTGACAGCCT
3' ss Score
7.26
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
Exon sequences
Seq C1 exon
GTAAAGTGAATATCACTGTAGTTGCTGAGTCCAAACAAAGCAGTGCTTGCCCAAATGAAGGAATGGAGCAGCAAAAGCTAAACTGGAAAGACACTGTGGTCAAAAGCTTCTTAGTAGAG
Seq A exon
CCTGAAGGTATTGAAAAGGAAAGGACCCAGAGTTTCCTTATCTGTACAGAAG
Seq C2 exon
GTGCCAAAGCCTCCAAGCAGGGAGTTTTGGACTTGCCAAATGATGTAGTAGAAGGGTCAGCCAGAGGCTTTTTCACTGTTGTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177359_MULTIEX1-27/38=26-28
Average complexity
C1
Mappability confidence:
89%=100=90%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.125 A=0.000 C2=0.000
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
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGTGCTTGCCCAAATGAAGGA
R:
CCTCTGGCTGACCCTTCTACT
Band lengths:
145-197
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development