Special

HsaINT0076964 @ hg38

Intron Retention

Gene
ENSG00000122566 | HNRNPA2B1
Description
heterogeneous nuclear ribonucleoprotein A2/B1 [Source:HGNC Symbol;Acc:HGNC:5033]
Coordinates
chr7:26193251-26193694:-
Coord C1 exon
chr7:26193575-26193694
Coord A exon
chr7:26193374-26193574
Coord C2 exon
chr7:26193251-26193373
Length
201 bp
Sequences
Splice sites
5' ss Seq
GAGGTAATA
5' ss Score
7.96
3' ss Seq
GTATTCCAATTTTTTAATAGGAA
3' ss Score
7.95
Exon sequences
Seq C1 exon
GTGGCAATTTTGGAGGTAGCCCCGGTTATGGAGGAGGAAGAGGAGGATATGGTGGTGGAGGACCTGGATATGGCAACCAGGGTGGGGGCTACGGAGGTGGTTATGACAACTATGGAGGAG
Seq A exon
GTAATAAATTCACCTGCAACCTTTATGTGGGAATTTGGAATTAATGTCTTTGTAACACTTGATCTTTTGTTTCCATGTTTGTCACTAGATGCCCATAAAATTTGTGGATAAGTGTTTGCTTTTATTTGTTTTTATGGGAGCTTTGTCCTAAGTCCTTGGTTTAATGTTTGTATTGTTCTGAGTATTCCAATTTTTTAATAG
Seq C2 exon
GAAATTATGGAAGTGGAAATTACAATGATTTTGGAAATTATAACCAGCAACCTTCTAACTACGGTCCAATGAAGAGTGGAAACTTTGGTGGTAGCAGGAACATGGGGGGACCATATGGTGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000122566:ENST00000354667:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.638 A=NA C2=0.624
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:
GTGGCAATTTTGGAGGTAGCC
R:
CCCCCATGTTCCTGCTACCA
Band lengths:
228-429
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development