Special

HsaINT0016838 @ hg38

Intron Retention

Gene
Description
bromodomain adjacent to zinc finger domain 2B [Source:HGNC Symbol;Acc:HGNC:963]
Coordinates
chr2:159349007-159350357:-
Coord C1 exon
chr2:159349708-159350357
Coord A exon
chr2:159349281-159349707
Coord C2 exon
chr2:159349007-159349280
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:ENST00000392783:28
Average complexity
IR
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


Other Skipping Isoforms:
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