HsaINT1015764 @ hg38
Intron Retention
Gene
ENSG00000122566 | HNRNPA2B1
Description
heterogeneous nuclear ribonucleoprotein A2/B1 [Source:HGNC Symbol;Acc:HGNC:5033]
Coordinates
chr7:26197622-26197866:-
Coord C1 exon
chr7:26197831-26197866
Coord A exon
chr7:26197733-26197830
Coord C2 exon
chr7:26197622-26197732
Length
98 bp
Sequences
Splice sites
5' ss Seq
AAGGTACTC
5' ss Score
7.46
3' ss Seq
AATGGTATTTTCCTTTGCAGAGA
3' ss Score
9.82
Exon sequences
Seq C1 exon
AAAACTTTAGAAACTGTTCCTTTGGAGAGGAAAAAG
Seq A exon
GTACTCTGCCAGCAGGTCACCTCATATTTAAGAATTTAATTTCCTGCATACAAAGAGGAAAATGTAAATAAAAATTGAAATGGTATTTTCCTTTGCAG
Seq C2 exon
AGAGAAAAGGAACAGTTCCGTAAGCTCTTTATTGGTGGCTTAAGCTTTGAAACCACAGAAGAAAGTTTGAGGAACTACTACGAACAATGGGGAAAGCTTACAGACTGTGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000122566:ENST00000354667:2
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.833 A=NA C2=0.000
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
PF142591=RRM_6=PU(40.0=75.7)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACTTTAGAAACTGTTCCTTTGGAGA
R:
ACACAGTCTGTAAGCTTTCCCC
Band lengths:
143-241
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains