Special

HsaEX6066503 @ hg38

Exon Skipping

Gene
Description
disco interacting protein 2 homolog B [Source:HGNC Symbol;Acc:HGNC:29284]
Coordinates
chr12:50721273-50724886:+
Coord C1 exon
chr12:50721273-50721396
Coord A exon
chr12:50723202-50723323
Coord C2 exon
chr12:50724775-50724886
Length
122 bp
Sequences
Splice sites
3' ss Seq
CAGGGTCCTTTGTCTTGCAGGCA
3' ss Score
9.22
5' ss Seq
GATGTAAGT
5' ss Score
9.11
Exon sequences
Seq C1 exon
GGAACCACTGTATGCACAGCCAGCTGCCTTCAGCTTCATAAGCGAGCAGAGAGGATTGCATCTGTTCTTGGTGATAAGGGACATCTAAATGCAGGAGATAATGTGGTGTTGCTCTATCCACCTG
Seq A exon
GCATTGAGTTAATCGCCGCCTTCTATGGCTGCCTGTATGCGGGCTGTATACCTGTGACCGTCAGACCTCCACATGCTCAGAACCTCACGGCCACGCTGCCCACTGTCCGAATGATTGTTGAT
Seq C2 exon
GTCAGCAAAGCAGCCTGTATTCTCACCAGTCAGACCCTAATGAGGCTACTGAGGTCCCGAGAGGCAGCAGCAGCTGTGGATGTGAAAACCTGGCCAACCATCATTGACACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000066084-'58-70,'58-69,60-70
Average complexity
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=0.000
Domain overlap (PFAM):

C1:
PF0050123=AMP-binding=FE(8.6=100)
A:
PF0050123=AMP-binding=FE(8.4=100)
C2:
PF0050123=AMP-binding=FE(7.8=100)


Main Inclusion Isoform:


Main Skipping Isoform:
ENST00000301180fB13809


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGTATGCACAGCCAGCTGC
R:
CTGTGTCAATGATGGTTGGCC
Band lengths:
229-351
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains