Special

GgaINT0102643 @ galGal4

Intron Retention

Gene
Description
myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 [Source:HGNC Symbol;Acc:HGNC:16063]
Coordinates
chr2:17819902-17821428:-
Coord C1 exon
chr2:17821311-17821428
Coord A exon
chr2:17819975-17821310
Coord C2 exon
chr2:17819902-17819974
Length
1336 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGC
5' ss Score
9.88
3' ss Seq
GTGAAATATTTACACTGCAGATC
3' ss Score
5.78
Exon sequences
Seq C1 exon
GCAAACACCCTACCTGGATCATCTCTCAGTCTGCCTCCATCCCATATGTATGGCAATAGGCTGAATCCAAATTCAGCAATGGCAGCACTTATAGCTCAGTCTGACAACAGCCAAGCAG
Seq A exon
GTAAGCTACCCGGTGGTGGTGAAAACACTGACACTTCACAAACTGAAGAAACTCGAGTATTTGTAAGAAGATCGTAAGGTTTTATTCTTGAACTCCGCTCAGCATTTGGTTATTAAGAGTCTGTTTAAAGTTGTTAGGCGTTGCGAGTAAAGTCTTGGTAGGTCAGAACAGCTTTTTTTTTTTTTTTTTTTCCCCAACTTTCTGAAATGTAAATGTTTAAGCAGAGCCATCAGCAGGCAGGAATGCAACAATGTCTCCTGTGACTTCGGTGATTGATGTGTTCAGTTCTTAGCTCTTTGCAATGAGAGCAACACAGCTCTGGGTTTTGTCGTGAATAGTTTAAACCTCGATTTGCATAATTCATGAAATTGCATTACATACAACTTGGTGTGAAAGAGATCCCGTTAGAGAACTTCTACAGCATTCAGTAATCTTGTGAATATTTACCAATTGACATTTTTGTAACATTCGGGCTCCTCTCCGGTTTTAATGAGCCACTGGATTTGCTTTGTTTCATTCCATCCTAGGGATTTGTTGACATGTCGTAGTAGTCATGCCTGTTTGGGGGAAGGGAATGAGTTTAGCAGTTTACCAAGAATGGATCAGTCATGTCTTTGCCCTCCAAGAGGTCGGGGGTCACTTGACTCAGAATAGGGGGAGGGCAACCTTGAAGGGGGCAGATAGGGTTATTTTATTGAGAGGCCATAGGGAAAATAACCCTTTTGAGTCCTTCCAAGCAAAACGTTTTCGTATATTTAATGAGGCCTTTTTTGTTTGTTTTACTACGTTTTTAGCGAGGGACTTTCCTATGCTTCAGCTTATAAATAGGAATTTGTGAATTAGACGCTTCCATAAAGTTTTCAGTAAATTTGCAGAGCAGCACGTGCTTGTTAGATGGTAGCGGTAAGTTTAGCACGTTTCCTATTTTACGAGTTGTTTTGGGATGCAAAGTGTTAAAAAAAATACAGAGCATCAGGATTTGCTGTGATAAGCATACAGATTAGCTGTCCACAGCTGTGATTCATTACTTTCACCGTAGAAATTAAAAGTGGCTGAGGGGAGGGTACTGCAAATGCAAACCACGCTTCTGTGCTGTAAAACTGAAAGGAATGAAAGAAGTGAACATAATCCATGGCCTGGTACAGCCTCAGAAATGTGTAAGGACAACACCTTACATGCTACAGTTCAGCAATCTTAAACTAGTTACGGCTTCGCTCTTCAGTTGAAACTGCGGAGGGAAGTTAAGATTTAAGATATTTTTAAGATATCTGCGTCAGCTTCAAAACTCTTATCTAAGAAGAGTCGATTTATCAGCTGTGAAATATTTACACTGCAG
Seq C2 exon
ATCAAGATGTGGGAGATAACGGCCGCAGCCTTGCTGGCAGAGGAGGCTCGCCCAGAGGAAGTCTCTCGCCACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000007928:ENSGALT00000012873:12
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.925 A=NA C2=1.000
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
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCAAACACCCTACCTGGATCA
R:
CGTGGCGAGAGACTTCCTC
Band lengths:
191-1527
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]