Special

GgaINT0000892 @ galGal3

Intron Retention

Gene
Description
NA
Coordinates
chrE22C19W28_E50C23:64874-66413:-
Coord C1 exon
chrE22C19W28_E50C23:66057-66413
Coord A exon
chrE22C19W28_E50C23:65345-66056
Coord C2 exon
chrE22C19W28_E50C23:64874-65344
Length
712 bp
Sequences
Splice sites
5' ss Seq
GTGGTCAGT
5' ss Score
4.85
3' ss Seq
TGTGACCTCTTCTCCCTCAGGTG
3' ss Score
11.66
Exon sequences
Seq C1 exon
CTGAGAGTCTTCAAACTGGCCAAGTCCTGGCCCACTCTGAACATGCTGATAAAAATCATCGGTAACTCAGTGGGTGCTTTGGGCAACCTGACCTTGGTGTTGGCCATCATCGTCTTCATCTTTGCGGTGGTGGGCATGCAGCTCTTTGGCAAAAACTACAAGGAGTGTGTCTGCAAGATCAATCCGGAGTGTGAGCTACCCCGCTGGCACATGCACGATTTCTTCCACTCCTTCCTTATTGTCTTCCGTGTGTTGTGTGGGGAATGGATTGAGACCATGTGGGATTGCATGGAGGTGGCAGGACAGGCCATGTGCTTGATTGTCTTCATGATGGTCATGGTCATCGGAAATTTAGTG
Seq A exon
GTCAGTAAATGGTTACTGATGGTCTTTATCATTTTTTTTTTTTCTGGGTGGGGTAGAGCATGGGGAGACCACAGGACTGGGGCGGAACATGGGGAGACCACAAGTCTAGGCAGCCTCTTCCAGTTTGGTTGGGGTCCTTCATGGCCTGTGATGGATGAACAGTCCTGTTGACTTTGGTAGTACAGTATTAAGGCCTTAGCCAGTTGCCCACAAAAACAGCATCCAAGAAGCATGCAGTAAAAGCTTTTCAAATTCCAGGAGAGGAAAGTCCTGAAGTGCTAAAATAAGGTTGGAGGTTTCTTCTAAAATCTGCTAGTTCAATCCTGCAGCGTTATTGTATGCAAGAAGGGGCTGTTGAAATGGCACAGGCTGTCATGTGGGAGCTCAGACTGGATCAGAATGTTTCTCTCTAGACTTGTATTTTGTGAAGAAAAGTCTGTGGAGGAAAACATAAACAAGAATGAAGCAGAGTGACCGGTTGCATATCTTACAAGTAGAGTTTGAGCCTTATCTGGAAGGACTTGTTTCTCACTAAAGGGATTTAAACAAAACGAGCACTGGGACTACCAGTAGATGTGGGCAAGGAAATAAATCTGGGAGTGATCCCTCAAAATGCCCCTGTGTGGCACATTTCCTTCGAGCTTTAGATGGGCCCAAGGTGGAAATATTGTCCTCGTGTAGGCTCTGCCAAGTGTGACCTCTTCTCCCTCAG
Seq C2 exon
GTGCTGAACCTGTTCCTGGCTTTGCTGCTGAGCTCCTTCAGTGCAGACAACCTGGCAGCAACGGATGACGATGGGGAGATGAACAACCTGCAGATCTCTGTCATTCGCATCAAGAAGGGCATTGCCTGGACCAAGGCGAAAGTGCGTGAATTCATGCAGGCTCACTTCAAGCAGAGAGAGGCAGATGAGGTCAAACCCTTGGACGAGCTGTATGACAAGAAGGTGAACTGCATTGCCAACCACACGGGGGCTGATATCCACAGAGACATCGATTATCAGAAGAACGGCAATGGCACAACCAGTGGAATTGGGAGCAGCGTGGAGAAATACATCATCGATGAAGACCACATGTCCTTCATCAACAACCCCAACCTCACCGTCCGGGTGCCTATTGCTGTCGGGGAGTCAGACTTTGAAAATCTCAACACAGAAGATTTCAGCAGCGATACAGACCCTGATGGCAGCAAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000006060:ENSGALT00000009776:16
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=0.197
Domain overlap (PFAM):

C1:
PF0052026=Ion_trans=FE(62.1=100)
A:
NA
C2:
PF0052026=Ion_trans=PD(4.2=5.1),PF065128=Na_trans_assoc=PU(61.0=84.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGTGTTGGCCATCATCGTCTT
R:
ATCTCCCCATCGTCATCCGTT
Band lengths:
342-1054
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]