Special

HsaEX0055021 @ hg19

Exon Skipping

Gene
ENSG00000177359 | RP11-551L14.1
Description
NA
Coordinates
chr12:31270354-31286102:-
Coord C1 exon
chr12:31286051-31286102
Coord A exon
chr12:31285179-31285262
Coord C2 exon
chr12:31270354-31270418
Length
84 bp
Sequences
Splice sites
3' ss Seq
AATCAGTATTTTCATTCTAGGTG
3' ss Score
7.25
5' ss Seq
TGGGTAAGT
5' ss Score
10.24
Exon sequences
Seq C1 exon
CCTGAAGGTATTGAAAAGGAAAGGACCCAGAGTTTCCTTATCTGTACAGAAG
Seq A exon
GTGCCAAAGCCTCCAAGCAGGGAGTTTTGGACTTGCCAAATGATGTAGTAGAAGGGTCAGCCAGAGGCTTTTTCACTGTTGTGG
Seq C2 exon
TAAGGTACCTGCCGTGGGCAGATCTGAGCTTTCTTCTTGGACACCCCATACCCACAGTCCTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177359_MULTIEX1-28/38=27-35
Average complexity
C2
Mappability confidence:
89%=100=89%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.000 C2=NA
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
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGGTATTGAAAAGGAAAGGACCCA
R:
CTGGAGGACTGTGGGTATGGG
Band lengths:
112-196
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