Special

HsaEX0042207 @ hg19

Exon Skipping

Gene
Description
nudE nuclear distribution E homolog 1 (A. nidulans) [Source:HGNC Symbol;Acc:17619]
Coordinates
chr16:15781232-15788113:+
Coord C1 exon
chr16:15781232-15781368
Coord A exon
chr16:15785001-15785180
Coord C2 exon
chr16:15788022-15788113
Length
180 bp
Sequences
Splice sites
3' ss Seq
GAATCCTTTTTCTGGCACAGATT
3' ss Score
6.39
5' ss Seq
GTGGTAAGG
5' ss Score
8.37
Exon sequences
Seq C1 exon
CGCCACGATCATGTCTCTCGAAGACTTTGAGCAGCGCTTGAATCAGGCCATCGAAAGAAATGCCTTCCTGGAAAGTGAACTTGATGAAAAAGAGAATCTCCTGGAATCTGTTCAGAGACTGAAGGATGAAGCCAGAG
Seq A exon
ATTTGCGGCAGGAACTGGCCGTGCAGCAGAAGCAGGAGAAACCCAGGACCCCCATGCCCAGCTCAGTGGAAGCTGAGAGGACAGACACAGCTGTGCAGGCCACGGGCTCCGTGCCGTCCACGCCCATTGCTCACCGAGGACCCAGCTCAAGTTTAAACACACCTGGGAGCTTCAGACGTG
Seq C2 exon
GCCTGGACGACTCCACCGGGGGGACCCCCCTCACACCTGCGGCCCGGATATCAGCCCTCAACATTGTGGGAGACCTACTGCGGAAAGTCGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000072864-'8-12,'8-10,9-12
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.394 A=1.000 C2=0.555
Domain overlap (PFAM):

C1:
PF077956=DUF1635=FE(31.9=100),PF0030915=Sigma54_AID=WD(100=52.2),PF048808=NUDE_C=PU(25.6=87.0)
A:
PF077956=DUF1635=FE(41.8=100),PF048808=NUDE_C=FE(37.8=100)
C2:
PF077956=DUF1635=PD(18.4=83.9),PF048808=NUDE_C=FE(19.2=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GCCACGATCATGTCTCTCGAA
R:
CGACTTTCCGCAGTAGGTCTC
Band lengths:
226-406
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development