Special

HsaEX6066501 @ hg38

Exon Skipping

Gene
Description
disco interacting protein 2 homolog B [Source:HGNC Symbol;Acc:HGNC:29284]
Coordinates
chr12:50728548-50732536:+
Coord C1 exon
chr12:50728548-50728678
Coord A exon
chr12:50731369-50731537
Coord C2 exon
chr12:50732366-50732536
Length
169 bp
Sequences
Splice sites
3' ss Seq
TCTTGTCTCTTTCACTGCAGTGT
3' ss Score
9.12
5' ss Seq
AAGGTAAGA
5' ss Score
10.57
Exon sequences
Seq C1 exon
ATGTCCCACTCTGCAGTGAACGCTCTGTGTCGAGCCATCAAGCTCCAGTGTGAGTTGTACTCTTCTCGGCAGATCGCCATCTGCCTTGACCCTTACTGTGGACTTGGCTTCGCGCTCTGGTGTCTCTGCAG
Seq A exon
TGTCTATTCAGGCCACCAGTCTGTCTTAATTCCTCCTATGGAGTTAGAGAACAACCTTTTCCTCTGGCTCTCCACAGTCAACCAGTACAAAATAAGGGACACTTTCTGCTCCTATTCAGTGATGGAGCTCTGCACCAAAGGTCTTGGGAACCAAGTGGAAGTGCTAAAG
Seq C2 exon
ACCAGAGGGATCAACCTCTCCTGCGTCCGGACCTGTGTGGTGGTGGCGGAGGAGAGGCCCCGCGTTGCACTCCAGCAGTCCTTCTCTAAGCTCTTCAAAGACATCGGGCTGTCCCCGCGGGCTGTCAGCACCACTTTTGGATCAAGAGTCAATGTAGCAATATGTTTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000066084-'63-79,'63-77,65-79
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(9.0=100)
A:
PF0050123=AMP-binding=FE(11.8=100)
C2:
PF0050123=AMP-binding=FE(11.8=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTCTGTGTCGAGCCATCAAGC
R:
TCCAAAAGTGGTGCTGACAGC
Band lengths:
250-419
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains