Special

GgaINT0007911 @ galGal4

Intron Retention

Gene
ENSGALG00000002056 | C15H22ORF25
Description
chromosome 15 open reading frame, human C22orf25 [Source:RefSeq peptide;Acc:NP_001007837]
Coordinates
chr15:1263007-1263419:+
Coord C1 exon
chr15:1263007-1263126
Coord A exon
chr15:1263127-1263304
Coord C2 exon
chr15:1263305-1263419
Length
178 bp
Sequences
Splice sites
5' ss Seq
GAGGTATGA
5' ss Score
8.55
3' ss Seq
TCTGTGTACTTCTTTCTTAGGTG
3' ss Score
10.16
Exon sequences
Seq C1 exon
GTCTGGATATGGAGGAGGGAAAAGAAGGTGGGACGTGGCTGGGAATCAGTAAGAAAGGCAGGATGGCAGCCCTGACAAACTATATGCAGCCAACAACTGACAAAAATGCAAAAGGAAGAG
Seq A exon
GTATGATGGGATATTATTTATATTTTTTATTTCTCCATTTATGAAGGAATGTTTATTTTTTTTGCTTACTGTTACATTCTGTTGGTGGAAGATATCTTCTGTAGTATTGTTTGTTTTACCAAGCCTTTCGGATTAGTAAGTACATGTGGTCAAGTTGCTCTGTGTACTTCTTTCTTAG
Seq C2 exon
GTGCTCTTGTAACGAACTTCTTGACTTCAGATCTGGACTGTTACTCTTACTTGAAGAAAGTTTCAGTAGAAGGACATCTTTATAATGGATTTAATTTAATAGCAGCTGACTTGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002056:ENSGALT00000003199:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF057427=NRDE=FE(14.7=100)
A:
NA
C2:
PF057427=NRDE=FE(14.0=100)


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:
GTCTGGATATGGAGGAGGGAA
R:
AGTCAGCTGCTATTAAATTAAATCCA
Band lengths:
231-409
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]