Special

GgaINT0048238 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr7:21137196-21137789:+
Coord C1 exon
chr7:21137196-21137270
Coord A exon
chr7:21137271-21137690
Coord C2 exon
chr7:21137691-21137789
Length
420 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
ATAATTGATTTTTCTTTAAGGCT
3' ss Score
6.04
Exon sequences
Seq C1 exon
AAAGATGCTCTCAATTTAGAGGCCACAAGAATGGAGGCCCTGCATTTTCTGTGCAGAGAAGGAAAGATGCGTGAG
Seq A exon
GTGAGTCTTGTTGGTTGCAGACAGTTGAGCAGAATACAACCTTTGTTAGGAGTTAGATCCCACATTCACAATATGCTTTCGGTCTTCCTCCTCGTATACTGTGTTCATATTATACTGAAGCCCTAGCAAGATGTACAGATCTTGCTTGATGGGATTCTTCCATCAGCTCAGATTCAGCTCAAATTATTCACTTTTTGTAGAATATTTAAGGATATACAATGATCTGTTTTATTCTCTTTACTAATCAATGTATTTTTCTAGAAATTCCAGTGTTTTAGAAGATCGATGTAACTTCTATCTCTGAACACCGCTGAATATAAGTTGCAAAATACTGTTATGCAGTGAAATGGTTTTAGTGCATTTTATGTAGTGGTCCTAATCTGTTAATTCTTTCAATTATATAATTGATTTTTCTTTAAG
Seq C2 exon
GCTTCGGCAAGACTAAGTGACCTCATTAAAGCATTGGACAGGTTGGAGCCGCGTAATTCACAGCTCTTCTATAAAATGGCTTTAGCTTTCAGTAGAACA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000010956:ENSGALT00000017831:7
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:
PF145591=TPR_19=PD(19.7=52.0)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
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]