Special

BtaINT0093660 @ bosTau6

Intron Retention

Gene
Description
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 [Source:HGNC Symbol;Acc:HGNC:16063]
Coordinates
chr13:23117087-23119477:+
Coord C1 exon
chr13:23117087-23117190
Coord A exon
chr13:23117191-23119383
Coord C2 exon
chr13:23119384-23119477
Length
2193 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAAT
5' ss Score
6.41
3' ss Seq
TACTTGGCTTTTATTTTCAGTGC
3' ss Score
7.33
Exon sequences
Seq C1 exon
ACTTGCTATATTTGTGATGAACAAGGAAGAGAAAGCAAAGCAGCCACTGGTGCTTGCATGACATGTAATAAACATGGATGTCGACAAGCTTTCCACGTGACATG
Seq A exon
GTAAATATGATTTTGTCATTTTACAGAACTGAAATTGGGAATACCTTGTAAGTTAAAGACTTAGGTACCCAAATATTAAACTAAATTTTGTTGGTATAATTTCTATGTTTATATTTACTTACTGTAATAAAAATAATTCTAGTAATTGAGTGTATTTACCAGAGTGAATTTCCAGTAGGTAACCCTGGTTCTAGTGTCTTATTCTGTTTTATTTTGCCTAAGATATTTCTTTTGTTTACCTACCCTTTGATTTGTTATTAGGATTATAAGAACTGATGTAGATAAACTTAGTGCAGTGCCTGAAATACTAGTAAGAATTTAGTGAATGATTGTGTTTTTTTTCACTGCCTGAATTTCAAGAGGGGAAAAAAAGCAATCACCATCATTCTCTGTATTATAGTGGCTGTTCCTTAGAAAGTTTCTTAAATTTTTAAATGACCTTCTATTTTTATTTTGTTCATGCTTCCTTTTATTTTTTTTCATGTACATATTTGTTGCATAATTTTAATAGCAGTTTAAATGAAACATTGTTTTCTGATAATTTTTTTCACAAAAAAATTTTGATGAGATGATAGAAATACAGTCCATAGCAGCATGGGAATGACTACATTATATCCTATCAGATATTGGTATTTATTAACATTTCAGAGATTTACAGACACTTTGTTTCCAAATTGGTTCGTAATATGTGCTACTGTAAGGAACATTTTGTGCATTTAACAAATGTAAATTTAACTTCCTTAGAATACTAATTAATGATAATAACTGTCATGTATTGAGTATTTGGGTTTCCCTGGTGGCTCAGGTGGCAAAGAATTCTGCCTGCAGTGCAGGAGACCCTGGTTTGATCCCTGGGTTGGGAAGATACTCTGGAGAAGGAAATGGCAACCCACTCCAGTATTCTGCCTGGAGAATTCCATGGACAGTGGAGCCTTGAAGGTACAGTTCATGGGGTCACAAAGAGTTGGGCGTGACTGAGTGACTAATACACATTGAGTATTTACTATGAAATGGGCAGGTTTTTTTTTTTTTTTTTTTTAAATAAAAATATTTATTTACTTGATTGCTGCTGGTGTTAGTTGCAACATACAGAATCTTTAGTTGTGACATGGAAACACTTAGCTGTGGCATGTGGGTTCTAGATCTAGTTCCCTAATCAGGGACATAGAAAATAGACTGGTGGTTGCTAAGGGGGAGTGGGATGGGCGAGGGCAGGATTGAGAGTTTGGGACTAGTAGTTGTAGATGCAGACTAATAAGTACAGGATGGATAAACAACAAGGTCCTACTGTTAGAGCACAGGGAACTGCATTCAGTATCCTGTGATAAACTATAGTGGAAAAGAATATGAAAAAGAGTGTGTGTGTGTGTATGTATGTATAACTTAGTCACTTTGCTGTACAGCAGTAATTAACACAACGTTGTAATTCAACTATACCTTAGTAAAAAATAAATATTAAAAATTTCCTTAATATTGTAGTTAATTTTCCAAAGATGAAAGACCTTTTTTGGCTGTGAGATACATACTAGTACTATTATTTTGGAATGTTGAAAGTGGAAGGTCAAATTGACAATATGATGGTTATAAACATTAACACTTCATTAAAAATTACCATAGCTTTAGGTTTTAATTTCATTTCTTCCCTTGTTTTTGACTAGAAAAACACAGCTTCTGTTTTTCTTACCTACTCTACTATGTTATAACTTGAAGCATTTAACTTCTAACAATATGATCTGTGTTCAAGGTGAATACTGTCACGTGTCATGTCAGCCCTTTAGATACCTGGCCTTTTCTAATTGTACCTGTGATACAGATTGGAAAGTCAAATGAAGTGTTAAGTTTGGGGTGGTAAGGATATCTTTCAAGAAATTTAATGTCTATTTGGTGACTTAAAGCATGCAAGAATCTCTGTCCTTATTAGAGATGGATAAAAAGTTTATTTTAAACCATGTATATAGCTTTAAAAATATAGCAATCAAAAGATGGGGTGGAATGTTCTTAGTCTCAGCTAGAATAAAGCCTTTTATTTTCCCCTTTTCTCTTACGAGATACCTACGTGGTTGGAATTGAATTTTATGTATATATATACACATACACAAATACATAAATACATACACATAAAGTGTTTTATACACACACACATGTATATACTGTGGTTTAAATTTTGTTGATATACTTGGCTTTTATTTTCAG
Seq C2 exon
TGCTCAGTTTGCCGGACTGCTTTGTGAAGAAGAAGGTAATGGTGCAGATAACGTCCAATATTGTGGCTACTGTAAATACCATTTTAGTAAGCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000044074:ENSBTAT00000061645:6
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:
PF138321=zf-HC5HC2H_2=FE(28.8=100)
A:
NA
C2:
PF138321=zf-HC5HC2H_2=PD(22.9=84.4)


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:
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]


SPECIAL DATASETS

  • Pre-implantation embryo development