Special

GgaINT0134968 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr21:991186-991990:+
Coord C1 exon
chr21:991186-991311
Coord A exon
chr21:991312-991858
Coord C2 exon
chr21:991859-991990
Length
547 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGT
5' ss Score
10.47
3' ss Seq
TTTCTCTCTGATTGCTACAGCCT
3' ss Score
7.34
Exon sequences
Seq C1 exon
AGTGCCCAGCAGGGCGGTTCGGGGCCGGCTGCCTGCTGCTCTGCTCCTGCGGCGGGGCTCCCTGCGATGCAGTCAGCAGGAGGTGCGTGTGTGCACCAGGATGGACAGGGCACGACTGCGCCCAAG
Seq A exon
GTGAGTGCTTCTCGTGCCGTATGGCAGCAGCTGGAAGCCACTGACGGTGTGTGGATGTCCTGCTATGATAGTTCCACGTACAGAGAGCTGGCCCTGTCCCCAGCCCTGCAGCATCTCAGCTGCCCTGCTCAGCCCTCAGCAGTCTGCGTCCCTCGCACAGCTCCTGCAGGGTGACGGTGGCTGCCAGGTTAGGACGCTTTGCCAGAGCACTGCTCCCCAGCAGCAGATGTGAATCTCAAGTTGACACGAGGGCCCCGGCAGGCTAGCACTTACTGAGGGATGTTTATAAAACAAACACGGTGATGTTGTCCTTACTGCTAGCCGTGTGTTCCCAAACAGAAGCATACAAACCAGACAGGGAATCCACTACCAAGAAATTAGGCATCCCACCTTGCCCTTTTGGTTGCTAGCTCTCTGTACAGGGGTCTTGCAGCCCCTTCTCCCTGTCCGAGGGCAATGAGGAACGAGCCTAGCTGATAGCCCTCACCCCGCTCTGTGCTGCTTACCAAAGGCATTGAGCTGCCCTATTTCTCTCTGATTGCTACAG
Seq C2 exon
CCTGCCCAGAGGGTCGCTGGGGCCTCGGCTGCCAGGAGCTGTGTCCTGAGTGTGCCAACAACGGCAGCTGTGACCCCGCCACGGGAGCGTGCGTGTGCCCACCGGGCTTCACTGGCAGCCGCTGCCAGGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000001040:ENSGALT00000001544:14
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:
PF0005319=Laminin_EGF=PD(23.8=23.3),PF126612=hEGF=WD(100=30.2)
A:
NA
C2:
PF126612=hEGF=WD(100=28.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGCCTGCTGCTCTGCTC
R:
CAGCGGCTGCCAGTGAAG
Band lengths:
222-769
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]