HsaINT0103676 @ hg38
Intron Retention
Gene
ENSG00000078403 | MLLT10
Description
myeloid/lymphoid or mixed-lineage leukemia; translocated to, 10 [Source:HGNC Symbol;Acc:HGNC:16063]
Coordinates
chr10:21733504-21734129:+
Coord C1 exon
chr10:21733504-21733592
Coord A exon
chr10:21733593-21733767
Coord C2 exon
chr10:21733768-21734129
Length
175 bp
Sequences
Splice sites
5' ss Seq
CAGGTAATT
5' ss Score
8.55
3' ss Seq
TCTCTTCTTTCTTACGCTAGGAC
3' ss Score
9.8
Exon sequences
Seq C1 exon
CTCCTACTACTGATTCCTTGAACAGCAGTAAGAGCCCTCATATAGGAAACAGCTTTTTACCTGATAATTCTCTTCCTGTATTAAATCAG
Seq A exon
GTAATTTTTGTATGGTTATTTTCATCTATGTTGATTTACTTGTGAATAATAGTATATTAAATGGTTTAAAATTATTTTAAACAGTTTTGCAGTGTTCTTTAAACTTAGTTTCTCTTCTTTCTTACGCTGGGACTTAATGTCCAGTGGACTTAGTTTCTCTTCTTTCTTACGCTAG
Seq C2 exon
GACTTAACCTCCAGTGGACAAAGTACCAGCAGCTCATCAGCTCTTTCTACCCCACCTCCTGCTGGGCAGAGTCCGGCTCAACAAGGCTCAGGAGTGAGTGGAGTTCAGCAGGTCAATGGCGTGACAGTGGGGGCACTAGCTAGTGGAATGCAGCCTGTAACTTCCACCATTCCTGCCGTGTCTGCAGTGGGTGGAATAATTGGAGCTTTGCCAGGTAACCAACTGGCAATTAATGGCATTGTAGGAGCTTTAAATGGGGTTATGCAGACTCCTGTCACAATGTCCCAGAACCCTACCCCTCTCACCCACACAACCGTACCACCTAATGCAACACATCCAATGCCAGCTACACTGACTAACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078403:ENST00000377072:20
Average complexity
IR
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.933 A=NA C2=0.587
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CCTTGAACAGCAGTAAGAGCCC
R:
GGTGGAAGTTACAGGCTGCAT
Band lengths:
242-417
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development