Special

GgaINT0098632 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr2:106317299-106317948:+
Coord C1 exon
chr2:106317299-106317436
Coord A exon
chr2:106317437-106317901
Coord C2 exon
chr2:106317902-106317948
Length
465 bp
Sequences
Splice sites
5' ss Seq
AAGGTAATG
5' ss Score
8.99
3' ss Seq
GTTTTTTAAATTTCATGAAGGAA
3' ss Score
4.53
Exon sequences
Seq C1 exon
CATGTCAGTGCTCTCCTCTCGGTTCCCGGCACAGCATTTGTGAGCCAACAACGGGGCAGTGCGAGTGTCAAACAAACGTTACAGGGAGACAGTGTGACAGATGTATTTCTGCAGCCCCCAATTTCCCCTACTGTGAAG
Seq A exon
GTAATGCTTGAGATGGAAAATCCTCCATTTGATTCATATCACTCCCCATTTTTACTGTGGGGTTCTCCTGGACGTTCTGCTTTGTGGAATTTTGTGGAAACTCGCTGAAGTGTGGGAAGGGAGGGCCACGCAGGGAGTCACAAGGAGTGCATATTAGATGAGTTCATTCATCATTCTATATGTAATTCTAAGAAAATATCTCTCAGTTGTAGGTTGGTGCTATATTTTTCCAAGTGACTGCTTTGCATACCGAAACAAACAGTCTAAACTAGGCTAAATAAACATTTGAATAACCATTATAAAAGGGTTCTGGTGGTCTTTAAGTATTTAAGTCACTCCAGGATGACTGGATTAAAGAGCCCTTTGAAAGTTGCGAATGTTATCTTGTGCTTTTCCATTACTGTATTTCACAGCTGTTCTCAAAAGATCTTTTAATGTTTTGTTTGTTTTTTAAATTTCATGAAG
Seq C2 exon
GAATCAACAGTGAATGTAACCCTTCAGGTAGCGTCGATTCTCATTCT
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015056:ENSGALT00000024287:13
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(0.1=0.0),PF0005319=Laminin_EGF=PU(93.8=95.7),PF0005319=Laminin_EGF=PU(5.9=6.4)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(4.2=12.5),PF0005319=Laminin_EGF=FE(29.4=100)


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:
ATGTCAGTGCTCTCCTCTCGG
R:
AATGAGAATCGACGCTACCTGA
Band lengths:
182-647
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]