Special

GgaINT0098567 @ galGal4

Intron Retention

Gene
ENSGALG00000011036 | HNRNPA2B1
Description
heterogeneous nuclear ribonucleoproteins A2/B1 [Source:RefSeq peptide;Acc:NP_001026156]
Coordinates
chr2:32318761-32319240:-
Coord C1 exon
chr2:32319121-32319240
Coord A exon
chr2:32318884-32319120
Coord C2 exon
chr2:32318761-32318883
Length
237 bp
Sequences
Splice sites
5' ss Seq
GAGGTAACC
5' ss Score
8.55
3' ss Seq
TTCTTGTATTGATTATTCAGGCA
3' ss Score
5.77
Exon sequences
Seq C1 exon
GTGGCAACTTCGGTGGCAGTCCTGGTTACGGAGGAGGAAGAGGAGGATATGGTGGAGGAGGACCTGGATATGGCAACCAGGGTGGGGGCTATGGAGGTGGCTATGACAACTATGGAGGAG
Seq A exon
GTAACCTACTGGCTTGAAGTGATCAAGTTTCAGTTGTAAATTAGTGCAAATCATATGAAATTTGGGAGGTTTATGGTGGAGTAAGCAAGCTCAATTTTATAAATGGAATGAAAAAGCAGCTGATTTTACGTGCTGCTGGACTACTTGTATCATTTTGTCTTTTAATTGTGTAATAAGGAGAATTCTGTGGACATTGTAGCTCATCCAGACATGTCTATTCTTGTATTGATTATTCAG
Seq C2 exon
GCAATTATGGAAGTGGAAACTACAACGACTTTGGAAACTACAACCAGCAGCCTTCTAATTATGGTCCAATGAAGAGTGGAAATTTTGGTGGCAGCAGGAACATGGGGGGACCATATGGTGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011036:ENSGALT00000017975:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.756 A=NA C2=0.738
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGGCAACTTCGGTGGCAG
R:
CCCCCATGTTCCTGCTGC
Band lengths:
228-465
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]