HsaEX6090537 @ hg19
Exon Skipping
Gene
ENSG00000197893 | NRAP
Description
nebulin-related anchoring protein [Source:HGNC Symbol;Acc:7988]
Coordinates
chr10:115422438-115423794:-
Coord C1 exon
chr10:115423570-115423794
Coord A exon
chr10:115423111-115423205
Coord C2 exon
chr10:115422438-115422525
Length
95 bp
Sequences
Splice sites
3' ss Seq
CTTCTCTATATGATTTCTAGATA
3' ss Score
6.89
5' ss Seq
CGCGTAAGT
5' ss Score
9.93
Exon sequences
Seq C1 exon
TCAGCAAAGGAAAGTGGAAGTTGGATTCTGAAAGATCGAGGTGCCCACAGGAATTTTATGGTCGTCGGATTTTGAAGACTTGAACTAGACTGGGGGTTCTCCTTGCATTTCTTGCCTGTTGCCTATCTTTGTCCTCTCTCTTCCGGCTTCGAGATGAATGTGCAGCCCTGTTCTAGGTGTGGGTATGGGGTTTATCCTGCCGAGAAGATCAGCTGTATAGATCAG
Seq A exon
ATATGGCATAAAGCCTGTTTTCACTGTGAAGTTTGCAAGATGATGCTGTCTGTTAATAACTTTGTGAGTCACCAGAAAAAGCCGTACTGTCACGC
Seq C2 exon
CCATAACCCTAAGAACAACACTTTCACCAGTGTCTATCACACTCCATTAAATCTAAATGTGAGGACATTTCCAGAGGCCATCAGTGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197893-'0-1,'0-0,1-1=AN
Average complexity
A_S
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=0.067
Domain overlap (PFAM):
C1:
PF0041217=LIM=PU(32.1=75.0)
A:
PF0041217=LIM=FE(55.4=100)
C2:
PF0041217=LIM=PD(8.9=16.7)
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTCTCTCTTCCGGCTTCGAGA
R:
TGGCCTCTGGAAATGTCCTCA
Band lengths:
172-267
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)