Special

GgaINT1011303 @ galGal4

Intron Retention

Gene
Description
disco-interacting protein 2 homolog B [Source:HGNC Symbol;Acc:HGNC:29284]
Coordinates
chrLGE22C19W28_E50C23:168182-169521:-
Coord C1 exon
chrLGE22C19W28_E50C23:169402-169521
Coord A exon
chrLGE22C19W28_E50C23:168297-169401
Coord C2 exon
chrLGE22C19W28_E50C23:168182-168296
Length
1105 bp
Sequences
Splice sites
5' ss Seq
CCTGTGAGT
5' ss Score
7.21
3' ss Seq
GAATATTTCTTTCTTTCTAGGGT
3' ss Score
9.76
Exon sequences
Seq C1 exon
CAAAAGTTGCTTTAGTCAAGTGTCGAGACTTGCACTGGGCCATGATGGCCCATCGAGACCAAAGAGACGTCAGTTTGAGTTCTCTACGCATGCTGATTGTAACTGACGGTGCAAATCCCT
Seq A exon
GTGAGTATGCTATACTGCTGTTCTCCAGAGAGATTTCTCAGCAAGTTATTACCACATGCTCAAATCTGACTCCTTTTGTAGATACTTGCAGAAGACATAAGTTAGGGTAGCTGCCTGGTAACACCAGAGTAGTGGTGTATGGGAACTGCTGAGCTGTGGTCTGAACCACTGATTGAGCATCTGGGAAAAAGACCCGGTCAGCCATAAGAGCACAGGTGAAGGCAGTTCACTCATGGGACAGGAAGGGGTGGAGCCTGGCTGCACCTCTCTTAGACCTCATTTAAGGGCTGACTGCCACTGAGGAAGGATCTCTTTTTGGAGGTCCCTCCTTGCTGAAGCTTCCCTCTGTGTTCCTGGCATCTTCTGATACAGGTGAGCAATCTTCTTCCCTTCATAGCACCTTTCTATCATGCTGGTCCTTCTGTCGTCACACCTCTTTTATAATGCCTTTCCTATTGTACTGATCTGAGTACTAGAGCAATGGGTTTTCTGTGCTTTCATCATGAGCTGTGAAGGATACTGCAAAGGCAGAAACAGAGCTCTTGTGTGAAGAACAGAATTCTGCTAGATATGGTGAGATAGGTTGTGAATTGCTGACTGTGACCAAAGTGAAGACTATTAAGAAGAAAATTGAAGGGGAAGAAATACACCAGAAGATTTGCAAGGATTACTGCTAGCAAAAAGTCATAAAAAAGTATTTGTCTAGGCCATACCAACTGGAAGGGGCTATTGGAATTACTGTTAGACCAATTCTTTATTACAACTACTGTATGGAGACAGAGCCCATGTATGTCTGCATACTGTTGGAAGTTTGGAAAGTATTTGAATTCTTGTTTTGTACTATTAATGTGTTGGGTTTTTTTTATTTCTTTATTAAAAACAAGCACCCTAAACCACTGCAGGGCAGAAAAACAGACTTGCTTTGTCACAAGTCCTGTTCAGTAGACACTGATGTCTTAGAGGATGTCACCTACAGTTTTTAGTAGTGATACCACATATATACTCTGCCAGTAAGCTGCACTTATTCCTAGGCTATTTTGGATACTTAAAAAAAAGTACATATATATATATAAAAGATTATAGTTGAATATTTCTTTCTTTCTAG
Seq C2 exon
GGTCTGTTTCCTCATGCGATGCCTTCCTGAGCTTGTTTCAGAGTCATGGGCTTAAACCAGAGGCAATTTGTCCGTGTGCCACATCTCCAGAAGCAATGACTATTGCAATACGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006139:ENSGALT00000009909:16
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:
PF0050123=AMP-binding=FE(13.1=100)
A:
NA
C2:
PF0050123=AMP-binding=FE(8.0=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAAAAGTTGCTTTAGTCAAGTGTCGA
R:
TAGTCATTGCTTCTGGAGATGTGG
Band lengths:
222-1327
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]