HsaEX0007737 @ hg38
Exon Skipping
Gene
ENSG00000123636 | BAZ2B
Description
bromodomain adjacent to zinc finger domain 2B [Source:HGNC Symbol;Acc:HGNC:963]
Coordinates
chr2:159398829-159404910:-
Coord C1 exon
chr2:159404849-159404910
Coord A exon
chr2:159400599-159400664
Coord C2 exon
chr2:159398829-159398894
Length
66 bp
Sequences
Splice sites
3' ss Seq
TATCATAACTTTTCCTACAGGAA
3' ss Score
9.9
5' ss Seq
GAGGTAGAA
5' ss Score
4.54
Exon sequences
Seq C1 exon
CAATAATGGCTGCTGAGGAGAAGCGGAAGCAAAAAGAACAGATAAAGATTATGAAACAGCAG
Seq A exon
GAAAAAATTAAGAGAATACAGCAAATCAGAATGGAAAAAGAACTTCGAGCTCAGCAAATTCTAGAG
Seq C2 exon
GCTAAAAAGAAAAAGAAGGAAGAAGCGGCAAATGCCAAATTATTGGAGGCCGAGAAACGAATAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000123636-'72-61,'72-59,79-61
Average complexity
S
Mappability confidence:
93%=90=100%
Protein Impact
Alternative protein isoforms (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=1.000 A=0.667 C2=0.964
Domain overlap (PFAM):
C1:
NO
A:
NO
C2:
NO
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAATAATGGCTGCTGAGGAGA
R:
TTTATTCGTTTCTCGGCCTCCA
Band lengths:
127-193
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