Special

GgaINT0039869 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr8:1329774-1330261:+
Coord C1 exon
chr8:1329774-1329897
Coord A exon
chr8:1329898-1330145
Coord C2 exon
chr8:1330146-1330261
Length
248 bp
Sequences
Splice sites
5' ss Seq
CAGGTACAG
5' ss Score
8.68
3' ss Seq
GCTTATTTCATGTTTTTAAGCGT
3' ss Score
6.81
Exon sequences
Seq C1 exon
GGAAAACCTGACGATAGTCACAGAGCTGGGTGATAGAGCAGCACAAGGACGTGCCTTTGGAAATCTGGGAAACACACACTACCTTCTGGGCAACTTCAGGAGTGCAGTTTTAGCCCATGAACAG
Seq A exon
GTACAGCAATGTGAAATATCACCAGTTGCTCCAGACCTCATATACATGTGTTTTGTTGCATACTCTCATGAGCTTTTTTAATGCAAGCTTTAGAGCTTAAGGCCTAGCATCAAGTCCGGCTGTTCTTTTCAAGCACTGTTGGGCAAAGAACAGATAAGGTTGGAAAGTCTACGGGTGTTCAGTTTTGTGTGCAAATGTATGTTATGAAGTACAAAATGTGATTAATATGCTTATTTCATGTTTTTAAG
Seq C2 exon
CGTCTCCTAATTGCAAAAGAATTTGGTGATAGATCAGCAGAAAGAAGAGCATACAGCAATCTTGGAAATGCCTACATATTCCTGGGTGAATTTGAAACTGCTTCTGAATACTACAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002090:ENSGALT00000003258:6
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:
PF134241=TPR_12=FE(68.3=100)
A:
NA
C2:
PF134241=TPR_12=PD(10.0=15.4),PF134241=TPR_12=PU(36.4=71.8)


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:
CGATAGTCACAGAGCTGGGTG
R:
TTGTAGTATTCAGAAGCAGTTTCAAA
Band lengths:
229-477
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]