Special

DreINT0003297 @ danRer10

Intron Retention

Gene
ENSDARG00000019707 | C21H9orf114
Description
chromosome 9 open reading frame 114 [Source:HGNC Symbol;Acc:HGNC:26933]
Coordinates
chr21:3645472-3646185:+
Coord C1 exon
chr21:3645472-3645511
Coord A exon
chr21:3645512-3646065
Coord C2 exon
chr21:3646066-3646185
Length
554 bp
Sequences
Splice sites
5' ss Seq
AAAGTAAGT
5' ss Score
9.72
3' ss Seq
TCTGTATTTCTTTCACCTAGAGA
3' ss Score
7.24
Exon sequences
Seq C1 exon
GGCGAAGAGAGAAAAAACTGGAAGAAATGGAAAGAACAAA
Seq A exon
GTAAGTGAGGAAATACTGGTGAAGTTAATTTTAGAAATGGTGTTATTTGTGTGTGTGTGTGGTCAAAAAGAAAGATGAAATTCTGAGTTAAAATGGTAAATGGCACATGGTAAGATCACGTATTATCAGCAAGGCATGACTACATGTGTTTTTCTGTATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATAATACACACACATTCAAAAAAACTATACAAAACTATTTTGTTACATAGATATTTAAATTTACATATTTACATTATATATTTAATTTCTTAATATAAATCAACTTTTTATCAAATATATGCGTGCATGTACACATCGCACACACACACATGCATATATTTCATGTCAAAACAAATGTTTATTTTGGTTGCGATTAATCAAGACTAGTTTAATCATTGCCCAGCTATAACAAATCTATCAAAGGCCTTTTAGCTACAAAATGTTATATAAACTTAAAACTCTTCCTGCTAAAAACTCATAAGGTCTTTCTGTATTTCTTTCACCTAG
Seq C2 exon
AGAAAGAAGAGAAGCGGCGACGAAAAGAGACCAAACTCATCCAGCAGCTGGAGAAACAGAAGCTGAAGAAAGAGGAGGAAAATCAACAGCAGGTTAAACAGGAAGAGAAGGAAAGTAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSDARG00000019707:ENSDART00000146754:3
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=0.772
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
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]