Special

BtaINT0093661 @ bosTau6

Intron Retention

Gene
Description
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 [Source:HGNC Symbol;Acc:HGNC:16063]
Coordinates
chr13:23119384-23121498:+
Coord C1 exon
chr13:23119384-23119477
Coord A exon
chr13:23119478-23121402
Coord C2 exon
chr13:23121403-23121498
Length
1925 bp
Sequences
Splice sites
5' ss Seq
CTGGTAAGA
5' ss Score
9.45
3' ss Seq
ATATATATTTTCTCTTTTAGAAA
3' ss Score
10.3
Exon sequences
Seq C1 exon
TGCTCAGTTTGCCGGACTGCTTTGTGAAGAAGAAGGTAATGGTGCAGATAACGTCCAATATTGTGGCTACTGTAAATACCATTTTAGTAAGCTG
Seq A exon
GTAAGAATCTGTCTTGAATTTAATTTACGATTATAATAATTAGGTTTGAATTGAGTCTTTATAAGGCATCCATTTTTGGGGGGTTGCTTTTGCTCCAGATTGAGTTTCTTAGTGTGTTGTTTGTTGGGAATTAAAAGCTGTAGTAGTTTTTTTTTTTTTTTAATTGGAGGTTAATTACTTTACAGTATTGGTTTTGCCATACATCACCATCAAGCTGTAGTAGTTTTAGAAGATTTTGCTTTGCTTGAGTTCATTTACAAAGGTGACTGTTCTAAAATATACTACTTTAGAATATATATTAATAGTTAATAGTAAATGTTGGTATCCATTTAGTAGAAAATAAAAATGTGGACATTTGATTACGTAATTTGTGATTCCCTGTCACTTTGTTTCATATCTTTTTGCTTTATTACTGTTACTAGTTTTATTACTTGTTTCATTTTTATTTGCTTGGAGGATAGTAACACTGAAACAAGGCTCTTTTGTAGCTTCTTCATTAAAGGTCTTCAGAAAGAAATATTTAAATACAACTTTGGGAATATTTTAGATTTGATTAGTCTTTACTGTCACATAGCATGGATAAGTTAGTACTATTTGATTAATCATTGTATATTCTGTGTCTGTGTTCCTTTGAAGGATCAATATTTCTTTAATTCCCCATTGTCTGTTTCTCAGTCTTTAGTTGATACCAGGTTTGTATACTGAAAATTAAAGGCTTCTTTGTTTTTCTTTAGTGTCTTCTTGTTATTTTTTATTGTTCCTTTTCTTCTGTGAATAGGGCTGTTTCTTTTTAGAAAAGGAACTCTTTTTTATGAAATGAGCAGCTTATGACTCCAGTATTTTGGCCCTTGCATATAAAATATTGAGAGTATATATGTATTATTTGATATTGAAGATACCAAATAACATATACTTACTGATTTATTTTTTTAATGACTGTCGAAGAACATCAAAGTCTTCTAGGAGAAATTTTGAGATAGTAAAATTGAAAATTCACTTAGGATATTAAAAGCATATTGGAATCTTCATTTTCTAAATCAGAGATAATATAGATAAAATATAGAAATAAGGAGAATGGGTTTTGGAATTTGTGCAAATAGAATTTTTTCATTGTTATTAATGTAATGTTATCCTATTTGGTGACTGGGGAAAAGTCTGTTTAATAATTTAATAAGATTGTATGAGCTCTATGTTTGCAAGGAATTTGATCATCTTTTATAGTCGTTTTTATCTAGCTTAATTAGTTATGGTACCACCAAGTTTTAACACCTGAAATAACTCTCACTGTCATACTTTATTATAAATCTGTGTAAGTCTTTTAAACAGAAATGTGTGTTACTTTTAGTATTGCTTTGAAAAATACATGAGTCTAATGCTGACATTTCCTTTTTTTCTCTATATGAACTACAGAGACAAATTTTTAGAAAATAGTATGCCTTAATACTGAAAGTGTGAGATTAAAAAGCTTCTTACTTTTCCTACTGGCATAAAGTAACTCTTAAAAATTTTTCTTTTCTTCTGGTTTTGGCATCCTTCTTCAGTATGGTATTTTCTATTTTTTGTTGAAATATCTTTTATATTTTAAAGCAGACATTGAAAACTATAGTTGATCTCTGTAATGAGGTGGTTTTATAATAAAATGACAAATAACCACTGCTTATTTGAAAATATTGTCTGTTTTCACACATTTTAATAAATGTACAAAAATATGGCATTAATGTTAGGTTAAGGGTTATATTTTCCTTTATAATGAAATAGATAATATATGGATTGTGTTGAATTGGATTATGTAGTTGGAAATAGCCTTTTTTTTTCTTTCGGTAGACATTTTAAAATATTTCACACTTGAATTGGTTTTAACCTAACAAAAAAGATTTAAAACTTTATATACATATACTTATATGTATATATATTTTCTCTTTTAG
Seq C2 exon
AAAAAGAGCAAACGGGGATCTAATAGGTCATATGATCAAAGTTTAAGTGATTCTTCCTCTCACTCTCAGGATAAACATCATGAGAAAGAGAAAAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000044074:ENSBTAT00000061645:7
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=0.781
Domain overlap (PFAM):

C1:
PF138321=zf-HC5HC2H_2=PD(22.9=84.4)
A:
NA
C2:
NO


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:
CTCAGTTTGCCGGACTGCTTT
R:
TCTCTTTCTCATGATGTTTATCCTGA
Band lengths:
183-2108
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development