Special

DreINT0017300 @ danRer10

Intron Retention

Gene
Description
proline-rich coiled-coil 2B [Source:HGNC Symbol;Acc:HGNC:28121]
Coordinates
chr5:71249787-71250476:-
Coord C1 exon
chr5:71250172-71250476
Coord A exon
chr5:71249966-71250171
Coord C2 exon
chr5:71249787-71249965
Length
206 bp
Sequences
Splice sites
5' ss Seq
ACGGTGCGC
5' ss Score
8.67
3' ss Seq
CTTTCGCTTCTTCTCTACAGATC
3' ss Score
11.17
Exon sequences
Seq C1 exon
TCACAGGAGATGACGGCTCAGAGTCAGGGTGAGGACTGGGAAACGGGTTCAGACAACAGTGATTTCGGTGACTGGCGGGAGAAGCGAGGGCCGCACGGGGATCCGCTGACAGACGCGGCTCTCGGAGATCCGGGATCTGAGAAGAGAGAACTCTCCAAACGCAGCTTTTCCAGCCAGCGGCCGCTGGACCGACAGAACCGCAAGAATGACGTGTCTGTGATGGAGAACAGCAAGATGGGCCGTCCGGCAGATGCAGGATCCAGAAACGACAGCTGGCAGAATGGAGTCGCGTCCGGCAGCAAACG
Seq A exon
GTGCGCCGCTTTATAGCATGAGCTCTAGATCTTCATTAAAGCAGAGCTGTTGATTAAGTGTGGCGTCAAGTGATTGCCTTAAACAGCAATGCTTTATTGGTATCTAACAACATGCACTAGGTTTGATTTCAGATGAACAAAGCTCTCAGATTAACTGCAGAATCTTGACCTTTGCGTGAACTAACCCTTTCGCTTCTTCTCTACAG
Seq C2 exon
ATCTCCAGAAGAGTCTGTCAGCGGTCTGAGCTCTGCGTCGGTGTACGGTGTGGAGCAGAACGAAGACCGCAGCACGCCTGAGCCCACAGGGAAGATCATAGAGAAAGAGTTGAAGCCCAGAAACATGAAGGCGGACATGACTGAACCGCTGTCCCAGTACGACCTCAACACTTACTCGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000079639:ENSDART00000112955:18
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 A=NA C2=1.000
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
Primers PCR
Suggestions for RT-PCR validation
F:
GACTGGGAAACGGGTTCAGAC
R:
TCAGACCGCTGACAGACTCTT
Band lengths:
301-507
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]