Special

GgaINT1029662 @ galGal4

Intron Retention

Gene
Description
villin-1 [Source:RefSeq peptide;Acc:NP_990773]
Coordinates
chr7:22034028-22034437:-
Coord C1 exon
chr7:22034258-22034437
Coord A exon
chr7:22034174-22034257
Coord C2 exon
chr7:22034028-22034173
Length
84 bp
Sequences
Splice sites
5' ss Seq
AAGGTGGGT
5' ss Score
8.23
3' ss Seq
CCATGCTGCTCACTCTGTAGGGC
3' ss Score
7.74
Exon sequences
Seq C1 exon
AACGGCTCCTCGCGGGCGGGCGGCACGGAGCCGGCGTCCTCCACTCGGCTCTTCCACGTGCACGGCACCAACGAGTACAACACCAAGGCCTTCGAGGTGCCCGTCCGAGCCGCTTCTCTCAACTCCAACGATGTCTTTGTGCTCAAGACGCCCAGCTCCTGCTACCTCTGGTATGGGAAG
Seq A exon
GTGGGTATGGCCTCGACCGGCTCCTCCTCGTCCTCCAGAGGATGGGGTGGGCTCGGTGCTGGAGCCATGCTGCTCACTCTGTAG
Seq C2 exon
GGCTGCAGCGGGGATGAGCGTGAGATGGGCAAGATGGTGGCCGACATCATCTCCAAGACGGAGAAGCCGGTGGTCGCTGAAGGGCAGGAGCCGCCCGAGTTCTGGGTAGCTCTGGGCGGCAAGACCAGCTACGCCAACAGCAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000011433:ENSGALT00000038192:13
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.067 A=NA C2=0.163
Domain overlap (PFAM):

C1:
PF0062617=Gelsolin=PU(47.8=55.0)
A:
NA
C2:
PF0062617=Gelsolin=PD(49.3=69.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCACCAACGAGTACAACACCA
R:
CTTGGAGATGATGTCGGCCAC
Band lengths:
173-257
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]