Special

GgaINT1014831 @ galGal4

Intron Retention

Gene
Description
human immunodeficiency virus type I enhancer binding protein 3 [Source:HGNC Symbol;Acc:HGNC:13561]
Coordinates
chr23:912304-915660:+
Coord C1 exon
chr23:912304-912964
Coord A exon
chr23:912965-915254
Coord C2 exon
chr23:915255-915660
Length
2290 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGT
5' ss Score
10.65
3' ss Seq
GGCCGTTTCTTTTTCCCCATCTG
3' ss Score
-0.16
Exon sequences
Seq C1 exon
ACCAGCTCTGACTTCCACCGAACAATTGGCTTCTGCTGAAAGAGAGTCTGTCACCAGGCCACCCATGTCCCTAGCCATGGAACTGTCAGCCTCAAAAGACACCTCCCCAAGGAAAAGGTGGTCTCCGAGCCAGGACTCCAGCAGAGCTGGCGGCAGCAGCAGACCAATGCTAGCGAGAAAGCATCTGTTAACCAAAAATGAAACTTCACCCAAACGGTTTTCACCCACCGGGGAGATGTCTCCTCTGAGGTGCCTGTCCCCAGGGAGAGGGCTGTCCCCGTGCCCACGTGTCTCTCCCAGGAGGGAGGCATCCCCGCTGCGGTGCGTGTCGCCGAGGCTCGAGCTGTCACCCAGCAGGCATCTGTCCCCCAGGAGAGAGCTGTCCCCCAGAGCGTACCTTCCTCCAGAAGGAGAGGCCTCATCTCCCAGCAGAGAGATGCCATCGGGCAGGTATTTATCGCTGAAGAAAACCTTGCCCCCGAGCTGCTCGGAGGCACCCAGGTACCCATCCCCTGGCAAGGAGGACGCGCCTGGGACAAGCAGATCGGCAGCAGATGACAAAATTCAAAGCTCATATCAAGCCCAGCATGGAATATTATCTTCGATGCCTCTACCTCACAGGTTCTTTGGCAAAAATGTACAGCTCTATGAATCCAAGCTG
Seq A exon
GTAAGTCCAAGCCCCCTCTTTCCCCTTATTATGTGCTGTGTTGTGATTTTAATCAAGCGTTGCAATGCAGAAGTGCAAAGTGACTGTAAACGTATACAGGGAAAAGTGAGAGTGAGCAGCAAAGGGTTTGCATCTGTTGGTCTGCCCATCTCAGCTGAGGGGAAATATAGTTGTCTCCTCTTCAACCCAATGCAGCTCTCCCTGACCCAACCCATTCTTGCTTTTCCTTCTGAGATAAGCAGTAAGGATGTGCGCTTAATAGAACTTGTCAAAGTTTTGCAGAGATCTTTTCCCTGGGAGTTTCAGGCCCATTTCTTAGATTTCACTAGCTAAAGTGAAACTCTACCCATTTTTCTATTGTCAGTGTCCTGAACCAGATTTGGACTAGCCAAGGGTCTCTCACACCTTGATGCTTTCTCCTGGGCTATGTACGCATGCAGCCCACAGTTAGATTAACTGCTGAGGAATGTTGGTTTGGACATCTCTGCTTTTATCTCGCCTCTCCAGCACAGAGAGGTTCTTCCCACTGCATCCAGAATATCATTTAATGTCTCTGTTGGACATATCAAATCCTATGGGTAAAGGAAAATTGCCTGTTCCTCCCACTGCTACAGGCAAATTAGACATTGGGTCTGGTGGAGCGCTGAGAGGTCTCCTATTCCTGCTGAGGTGCCTGGCTCTCCTGTAGTGTGTGCTGATGAACATGAGATCCAGCCCTGGAGGACCCATCACACAGATGCTGACTCAAGCGTTCCCCAGAAAAGCCCCGTTGCACCATTTGCCTTTCTGTCATGTCCACACAGTGAATCATCTCTTGGTGCTGCCTCCCTTCTGTTTCCCTCTATGAGTGTTTGCCTTACTTTCCCGGAGACCATCGATTTTTTTAGGCCCAAATTTTTGTCCACTTGAATTTCCCTCAGTTCTCAACTGCCTTTTGGGGTGAACCTCAGGGCTGTAAAGACCCCATTCCTTCTGTTCTGAAACATCTGTTAGGAAAACTACCCACTGGTGTCCTCTAAGCTCCCTAGTGCCCAAAGGAGGCAGTAGCACCTATTCCTGCTTACCTGCCCACTCCCACTTTTTTACTTACACTAACTTACCTTTCTGCTCATTGTCCTGCTCCTTTCAGAGCTGGGTTCTTCAGATCCCCAAATGGACCCCTGTGCTCCAAACTAGTGTCCTTTGTGGGAATGGTGTTCATCATTTAAAAACATAAAAACGATCTTAGCTGGGGCATAAGGCTTTTGTCCAGATCTGAGCATCAGGTCTCACTGTGGCTGTGCCTCTTCCCAAAGGCTCCTGCAACAGGTCATCTCTCCCCTTGGTAGCTGTTGTACCAGGGGGATTTGCTTGGGGTTTCCCAGCATCCCTACAGCAGTTCTGCCAAAACTTTGTGTGGATAAGTGTCACTGAGCAGGCACTGGGGCTGGTAAATGCTGACTAACTCATTGCTACCTTCTGTGGCTCTTGTTTCCTTTCTTCCTTTCTCTTTTGCTGCCTTCCTCTGCTGCCTTATCACAGAGATTCAGCTTGCAGGTCAGACAGTTTTCCATAGCTCCACAAAGGATTCCTCCAGTGAATCCTCAAATCCCATAACCCCATCTTTACAGAAAATTTATTTCATTTTCTGTAGCTTCCTCTTCCAGGGAGTCCTGTTTAGGGGTTTAGTTATAACCTCATCACTAATTAATCCATTTCTGTTTAGCCACATATCTCTCCATGATGTACATTAGGAAACTATGTGAAGCACCGGTCGGAGAAAAAGGAAAAGGTAAATTGGTAGGGTGCTAGCCTTGATTTCTGCAGACCACACCATGAGGGTGGTGGTGGGGACTGTTGATGGGAGTGCTTTGTGCCAGACCAGAGTTAATGCTCTCAGTGCAAAATATCCTTGCGATTAGCAGCTGTGAGAATGTAACACTGTTTTAAGGATATACATTAAAAATGGATAACAATGGTTTGGGCACTGAAGTAATTCATGTGCTGATGGAATGCAAGGATGCAGGGAGTGTTAATGTCTTCTGGTGGGATTTTGGAGGTGACTGATAATGACCGAACTACTGGGCCTGTGCCTCAACAGGCTGTGTGCCCGCTTGTACACCGAAGGCAAACACTGTGGGTTGTCTTGCTCCTTACCTTAAGGGTTTGGGAGCCCAATCCATCCTGGATTGATAGATCTCTTTCCAAATTAGAATAAAATGCGCGTAGAATCAATCCTTATAATGAGCGTTAATGATGCTAGTGCTGTACCTTATGCATTGCTCTGATCCGGCCGTTTCTTTTTCCCCAT
Seq C2 exon
CTGGTGCAGAAGATAGAACCCAGGAGCCCTCCACGCTCACCCGGCACCATGCAGCCCATCTGCTTCAGACCCTTGCAGGCACCTCACGAACTTCACACCCACAGCCGAGGAGAAGAGAATGTCTTCAGCCACCTTCCACTGCACTCGCAGCAGCTCGCAAGGACCCCGTACCCCATGATTCCCATCGGGGGCATCCAGATGGTCCAGGCCAGGCCAAGCACCCACCCCAGCTCCGTAATGTCCCTGCCAGGGGGACACTTTTCACCTGGTGGCAGTAGCTTTGAGGAGCCATGGGTGCCACGGGAGCCTTCATCTGCATCTGTCTCCCCGGTGGCAAAAGTTTCCAAATACACGCTGTCCCCAGAGCCTACAAGCAGTGAGTGCTTGGAGGAGAAAATGAGGACTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000027365:ENSGALT00000045163:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.905 A=NA C2=0.978
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
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]