Special

HsaINT0016838 @ hg19

Intron Retention

Gene
Description
bromodomain adjacent to zinc finger domain, 2B [Source:HGNC Symbol;Acc:963]
Coordinates
chr2:160205518-160206868:-
Coord C1 exon
chr2:160206219-160206868
Coord A exon
chr2:160205792-160206218
Coord C2 exon
chr2:160205518-160205791
Length
427 bp
Sequences
Splice sites
5' ss Seq
CAGGTTAGT
5' ss Score
8.02
3' ss Seq
TAAATGTTTTCTTTTTGCAGGTG
3' ss Score
11.11
Exon sequences
Seq C1 exon
GACTAGAAGAAATTGCAAAAGAAAGAGAAAAACTGAAAAAGGCAGAAAGTGTCCAGATCAAAGAAGAAATGTTTGAGACTTCTGGGGACAGTTTAAATTGTTCAAATACAGATCACTGTGAACAAAAGGAAGATCTTAAAGAAAAAGATAACACAAATCTATTCCTTCAGAAACCTGGCTCTTTTTCCAAATTAAGCAAGCTTTTGGAAGTAGCTAAGATGCCTCCTGAGTCAGAGGTTATGACCCCCAAACCAAATGCTGGTGCAAATGGGTGCACGTTGTCTTATCAGAACAGTGGAAAACATTCACTGGGCAGCGTTCAGTCAACAGCAACGCAAAGCAATGTGGAAAAGGCAGACTCTAATAATCTGTTTAATACTGGTTCAAGTGGTCCAGGGAAGTTCTACAGTCCTCTCCCCAATGACCAGTTACTAAAAACGCTGACTGAAAAGAATAGACAATGGTTTAGTCTTTTGCCACGAACACCCTGTGATGACACTTCACTTACTCATGCCGATATGTCAACTGCTTCTTTGGTGACTCCTCAGTCTCAGCCACCATCTAAGTCACCTTCACCTACCCCAGCTCCTCTTGGATCTTCTGCTCAGAATCCTGTTGGCTTAAATCCATTTGCTTTATCACCTCTTCAG
Seq A exon
GTTAGTACTGCTAACTGTAACTCATTTTTATATTGCTTTATGTAATCTTTGACCCCATGGAGATTTTTGCTCAAGGGGGCTCACTCAGATAGTTAAAATATTCCTGCTACAGTTTGAAAACTAAAACAAGTCAGAATTTCTGTCACCAAGGTTCATTAGAACTACTGATTTCTAGACTTTGTCTAAGTCTTCTTTAATTACTTTTTAACTTATTACTGTAACGGTATATCCGAAAGGAAAATTACTTTGGGAAACAAATAAGAACATGGAATTTAACATTTTTGTTGCTAATGTATTTTGTTTTCCTGTAATTGTAATAAATGAAAGAATATTTTTTGGAATTTGAAAAATAATTTCATATTCCAAACATTTTTCCTAACTTCTTAGAGTAATCTACTTTTCATTAATAAATGTTTTCTTTTTGCAG
Seq C2 exon
GTGAAAGGTGGAGTATCTATGATGGGACTTCAGTTTTGTGGATGGCCCACTGGTGTGGTTACTTCTAATATTCCATTTACATCATCTGTACCTAGTCTAGGATCGGGGTTAGGGTTATCAGAAGGAAATGGTAATTCATTCTTGACTTCCAATGTTGCTTCAAGTAAAAGTGAATCTCCAGTACCACAGAATGAAAAGGCCACTTCAGCTCAACCTGCAGCTGTTGAAGTAGCAAAACCAGTAGATTTTCCTAGTCCAAAACCTATTCCAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000123636-BAZ2B:NM_013450:28
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.797 A=NA C2=0.467
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCCTCAGTCTCAGCCACCATC
R:
GCTACTTCAACAGCTGCAGGT
Band lengths:
342-769
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