Special

BtaINT0093721 @ bosTau6

Intron Retention

Gene
Description
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 6 [Source:HGNC Symbol;Acc:HGNC:7138]
Coordinates
chr19:39941965-39944651:+
Coord C1 exon
chr19:39941965-39942058
Coord A exon
chr19:39942059-39944477
Coord C2 exon
chr19:39944478-39944651
Length
2419 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGT
5' ss Score
10.13
3' ss Seq
CCTCTCAATTCTCTCTGCAGAAG
3' ss Score
10.05
Exon sequences
Seq C1 exon
TGCCCAAATGGCAGGCCTGCTGTGTGAGGAAGAAGTACTGGAGGTTGACAATGTCAAGTACTGTGGCTATTGCAAATACCACTTCAGCAAGATG
Seq A exon
GTGAGTTTCATCTGGGCGTGAGTGGGTTGGTCAGCCATGGTTTAGAGGGTGTGGACTCTAGGGTGCCTGGATCTGGGAGGACAGACAGGGGAGGAAGGAACTATGTCCCTGCTCTTGAGGAACTCACCATTGGATGAGGAATAAATTTTAAGTACAGCCTGAGGGGTGAAGCAGAGTTGAGCCAAGCAGTCCATCCCAGAAGACAGAGCTCAGACCCTGCCTATCAGAGTCTAGGAGGCTTCAAGAAGAAGGCAGCATTTAAGCTGAGCCAACAATTAGAGCCAACATTTGTGAGGCTTACCGTGCCCCAGCCTCTGTACTAATCTCTTTACGTGTGTGTGTTTGTATGTGTGTGTGTGCACGTGGATGTGCGTGCTCTTGCAGTCCTCCCTAAGAACTGGGTGTACTGCATTTACCCATTTTACGGATGAGTAAGCTAAGACCCACTAAGGTTACGTGACTTATCTCACAGTTGGTATGTGGGATTTAGAAAAAAACAGTCTGAAGGTCCTCAGGAGCCTGCCAAGAAAGACAGGAATTCCAGGCAGAGGGATTGGCATGGATAAAGTCCCAAGATAAGAAAGACCATTCATAAGCAACAGAACAGGATGTTTGGTAGGGACAAGGCAAGAGATGAGGTGAAAAAGCTCAGGCAGGGCCAGAGCTGGACTTGCTTCTGCCTCAGGTTCAGGGGCCCACGGAGAAGTGGGAGAAGGGGTGCTAACCCATGTTGGTGGAGAGACCTGCATGTTTCAGAAGCGGTGGGGTGTCCTGGCTAGGTATGCTGTGGCCTGACTGGGAAAGCAGCTTGGACCTCACCCCCAGGCCACAGGCTTGTGAGGCTGCTTGTAAGCAAGAGGGTAACATGATCAGATTTGTTTTTTAGGAAGATTACCCTGGCAGCCACTGTGAAGCCAGATCCAAAGGGCTGAGGCTGGTGACTGGGAGACAGCTGCAAGAGAGGGGGGGATGGAGGGATGAGGCTGGATTCTAGAATTATTTCTAGATAGACTTGCCTACATGTGAGGGTGGCTGAGGAGGAGGAGTTGAGGGTGGCACATAGGATCCTGGCTCTTGATGCTGGATAGATGGGGCTTGAGCTCCTCAGGCAGTGGAGTGGACTTCTAGCATATGTCCTGGTCTGCCGCGGAGAGTCCCAGTTTGTGCCTGTTGCCTTGGTGTAATTATTAATAGCTCCTCCTTTCATTTTCAAAAGTGTCCTGGTTTGGATAAGTCATAAGGTCACCTTGGTTCAAGGTTAGATATCAACTTGGGGGCTTCCCTCATGGCTCAGGTGGTAAAGAATCCAGTTGCAATGCAGGAAATCCAGGTTTAGTCCCTGGGTCAAGAAGATCCCCTGGAGAAGGGAATGGCAACCCACTCCAGTACTCTTGCCTGGAGAATTCCATGGACAGAGAAGCCTGGCGGGCTACAGTCCATGGGGTTGCAAAGAGTCGGACATGACTGGATGACTAACACGACACTAAGACAAGGTAGGGAGCTTTGGTTTGGAATATAGCAGGTGTCAAGTGGAGCTGTTTAGATTTGGTGGCTGTGTTCAGATTTCAGGCCCCCATAGGTGTGGCAGCCCCAGGTGTATAAGGCTAGGGGTTGGGGGCTCAGGTATGAAGAGAACCATGAAATGGGGAGTTTAGAGCTTAGCAGAGTAGGAGTGATGCCCACTGCTGGGGAGCCACTGGGTCAGATGAGGCCTGAAACTAGTCTTTGAATTTGACAGTTGGGAGTTTGTGGGTGATCTTAGAAAGAACAGCTCTAAGTCTAGGACTGGTGAAGCCATCAGACCAGGCATTGGGGAGTCCAAGGCCCTGGCTGGGAGGAATGGTAGCACAGGGGTTGTTTAAGTGTTCCTTATGGATATTTCCATGCCTTGTTCTTAAGGGCAGCAGATCCTTTGGGACAAAAGGAAGCACTGTTTGGTGGAGGGCCAGGAAAAGAAGAGAAGGGGTGATGGCTGGAGCATAGTGTCTGGAGGGAAGGATGGGGTATGGGGAGCAGGGGCTCCCATGAGGGCCACCCAGGGAGGGAGGTTGAGGTGGGCCGAGGTCGAGTGCCTGAGAGGGGCCAAGAGGGCACCATGGAAAGAGGTGGTGGAGAGAGAGACATGGGCCGAGGCCCACCTCCATCCATGCCTGGTATCTGGCTGGGGCCGAGATTCCCCACCTCTTCCGGGCCTCAGTTGCTAAATCTGTGCCCTGGATAAGCCAGCTGGGCAGACTGTAGGATTTCGGGGCAGGGAATGCACTCTGTTGAGCAGAGTATCATTAAGGACACAGGGTCCTCTTGTGACAGGCAGGGTGGGGGTGGGGGTTGCTGACCCCCAGGATCACCTGATCTTCAAGAACCTTTCAGTAACCTACGGAGAGGAGGGTGTGGCAGTTCCTCTCAATTCTCTCTGCAG
Seq C2 exon
AAGACATCCCGGCACTCCAGTGGGGGCGGGGGCGGCAGCGGAGGAACAGGAGGAGGAGGGGGTAGCACAGGGGGAGGCAGCAGCAGCTTTATTGCTGGCCGGAGGAGCAGGTCGGCCTCCCCATCCGCCCAGCAGGAGAAGCACCCTTCCCACCATGAGAGGGGCCAGAAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000011532:ENSBTAT00000015325:6
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=0.948
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:
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