Special

GgaINT0098566 @ galGal4

Intron Retention

Gene
ENSGALG00000011036 | HNRNPA2B1
Description
heterogeneous nuclear ribonucleoproteins A2/B1 [Source:RefSeq peptide;Acc:NP_001026156]
Coordinates
chr2:32319121-32319711:-
Coord C1 exon
chr2:32319649-32319711
Coord A exon
chr2:32319241-32319648
Coord C2 exon
chr2:32319121-32319240
Length
408 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGC
5' ss Score
9.85
3' ss Seq
AAAGGATTATATTGTCATAGGTG
3' ss Score
3.37
Exon sequences
Seq C1 exon
ATGGGTATGGGAGTGGCCGTGGGTTTGGTGATGGGTATAATGGATATGGTGGAGGGCCTGGAG
Seq A exon
GTAAGCTTGCTTCTGTTTGTGTTTTTATTTTTTTCTCTCACTTAGAACTGCTATACATTCATTTACTATTCATGTAAAATTTCAGAGTGCCGTAGGTATTCCGTTGGCTTTAAGAAACACATAAATACTGGCTCACGTTATACCTGATGTGGGAAATTGCATGGTTATGTCTTGAACAACCACGTCCTTCTCTTTAGAATAGTAGCAAGTCACTTCATTGATGTTTTTAGGCAGTCTGGCTAGTGGGTTTTAGTCACAATTCAGTTAGGGTGGGAGTTGGATATGTATCTTCTTGAAACTCCTGCCCTTTTTGTTCCCCTGTAGACTTCTCAACAGAAAAATAGCCTGTGTAGAACTTGGTTACCTTCTACACTGGAAAGCTTATTTTAAAGGATTATATTGTCATAG
Seq C2 exon
GTGGCAACTTCGGTGGCAGTCCTGGTTACGGAGGAGGAAGAGGAGGATATGGTGGAGGAGGACCTGGATATGGCAACCAGGGTGGGGGCTATGGAGGTGGCTATGACAACTATGGAGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011036:ENSGALT00000017975:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.682 A=NA C2=0.756
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
Primers PCR
Suggestions for RT-PCR validation
F:
ATGGGTATGGGAGTGGCCG
R:
TCCTCCATAGTTGTCATAGCCAC
Band lengths:
182-590
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]