Special

GgaINT0098633 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chr2:106317902-106319437:+
Coord C1 exon
chr2:106317902-106317948
Coord A exon
chr2:106317949-106319337
Coord C2 exon
chr2:106319338-106319437
Length
1389 bp
Sequences
Splice sites
5' ss Seq
TCTGTAAGT
5' ss Score
7.96
3' ss Seq
TAACTCATTTCTGTCATTAGGGC
3' ss Score
7.66
Exon sequences
Seq C1 exon
GAATCAACAGTGAATGTAACCCTTCAGGTAGCGTCGATTCTCATTCT
Seq A exon
GTAAGTATTCTATTACTGCAGATAGCAGTATTTGTTAACAGTTCATGTACAGTCTAGGTCTTTGCTGAACACATTCACTTCATTCCCTAAGTGCCTGAAGCCTAATCTTCGACTGTGAAAGAATTACATAGGCTTATTTGCAGAGTGAGAGTGGAAATGACCTTTGTGTTTTGCTCTTTGATCATATCAATGCAATTCCAGCTTGAGGGTGACAGTGGTTGTTCTTTTTATATATTTTAAATGTGGAATATGCATACTGTTTATGTACTTGGTGCTCTAGAATAATAACATATACATGCAGATACGCATTTGTGCCTGTGCATGTCTGATTCTAGGTTGATATAGAGCATTTTAGCACCAAATTATTCTTGAAAAAAATATTCTTAGTAACTGCTGATATTCTGCTATTATCATTCTTAATACTGTGATAGTTATTAGTAGCATGCTATCAGAAATCAGAAGTCAGGATCAGAAACTGTTATAACCCATATATATGGGTTGTGGTGAAGACTGGCAGATGGAAGAGTTAGGCTCATGTATACATCTGTGTGTGTTTTCCACATTTTCTTTAAGTTAACCATACGTAAGCCAGTTACTCCCTGGGAACAGTGCTGATATATCTGAGCAAATAGTACTGCTGAAAGACATCCATGACTCCTTTGCAGAAAAGGATAGAAAAAAGAAGCTATGAAAAACAGAATTCTGTGGTATTTGCCTCTGCTTGTCCATAAGAACAGATGCATATAGGAGTAAAAAATGTTACTGTTGCCTCGGAAAAATATGCTTTAGTTTTTAATAATTATTTTTTCAATTATTTGTAAGTAGAGAATAGGAGAAAATATGACGAAGATAAGAAAAATTGTGCCTAAATCAATTTTACAGAAAGAAATGGACATCATATCTACTTCTAGTTAGTATGGCATTACTATAATTTGAAAAAATTACTGGTAATGTTAACATTTTTCATCTGAGTTGGTACGCTTTACTACTGTCTTTTCTACTCTGCCCTCCTAAGAAAAAGAGAGCAATAAGGGAGGGAAAAAAACATGAAAATTAATGATTACTTTTAAGGAAAATTGTATTTTTAAAGTTTTTACATAGCAGTTAATGCTTTAGAACAGTTCTAACAAGTCCATGAAAGAATTAGAAAGTGCAACTGTTGGGAGATTTAGAATAATTAGATATGGAAAAATTAGCAGTCTGAAACAATCCTGTGCTGATAGCATGAGAAAGAAAAATCTAAGGAGTGTGAATCTGCCTCAGTTTCCATGCTTCTGTGAAAGTCAGTAAGCTGCCTGAGTTGCTCTTAATATTTGATTATTCTTAGTAGTAAAAACTATGTGTTTCTGTGAAGCAGGTGAGTTTATATTAACTCATTTCTGTCATTAG
Seq C2 exon
GGCTATTGTCAGTGTCTTCAGCATGTTGAAGGTCCTACGTGTAGTAAATGCAAACCGTTGTACTGGAACCTGGCCGAAGAAAACCCTGAGGGATGTACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000015056:ENSGALT00000024287:14
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(4.2=12.5),PF0005319=Laminin_EGF=FE(29.4=100)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(60.8=91.2)


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]