HsaINT0103728 @ hg19
Intron Retention
Gene
ENSG00000108292 | MLLT6
Description
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 6 [Source:HGNC Symbol;Acc:7138]
Coordinates
chr17:36874098-36875836:+
Coord C1 exon
chr17:36874098-36874206
Coord A exon
chr17:36874207-36875769
Coord C2 exon
chr17:36875770-36875836
Length
1563 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGT
5' ss Score
9.8
3' ss Seq
CAGCCTTCCCTTCTTCCAAGAGC
3' ss Score
4.86
Exon sequences
Seq C1 exon
GTGTTTTCTCTGGCTGGCTCTACCTTTAGCCTCCCTTCTACCCACATCTTTGGAACCCCCATGGGTGCCGTTAATCCCCTCCTCTCCCAAGCTGAGAGCAGCCACACAG
Seq A exon
GTATGTGAATATCTGATCCCCTCTCCCCTTTCTTCCCAAAGGTCGGACACCCATCACCTGCATGTGACCCCAGAAAGAATGGGAGAGCTTTCTGGCTGCCCCCTCCCTCTGGCCATTGCCCTCCCTGCAAAAACAAACAGGCCGGGTGTGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGCCGAGGCGGGTGGATCACCTGAGATCAGGAGTTTGAGACCAGCCTGGCCAACATGGTGAAACCCCGTCTCTACTAAAAATACAAAAAGTAGCTGGGCGTGGTGGTGGGCGCCTGTAATCCCAGCTACTCAGGAGGCTGAGGCAGGAGAATTGCTTGAACGTGGGAGGCGGAGGTTGCAGTGAGCCGAGATCGCTCCATTGCACTCCAGCCTGGGCGATAAGAGCAAAACTCCGTCTCAAAACAAACAAAATCCCAGCGTAGTGGCTCCCGCCTGTAATCCCAGCTACTCAGGAGACTAGCCTGGGCAACACAGGGAGAACCTGTCTCTTAAAAAAAAAAAAAATCCACACACAGCAAACCAGGGTACACTTTCAAGTTAGAACCCAGCGAGAAGGCAGGGCAGGGAAGTTACTGCTCCATCTCACAGAAGAAAAAGGCAGAGATGGAAGACTTGCTCAAGGCAGGAAATGGCAGACCTAAAGCTCAGATTCTGTTCTCCTGACTCCAAGCCCAGTGCTTTCACCGGTGTAGCGTGCTTCCCCTTGGCTTCGTAGTGTGTCTTGGGATCAGCGCTTACGGAGGTCTCAACCTCTCCGGGTATTTACGAGTTAAGGGGGCGGGTCACAAGCGCCCCGCCCTCTCCCTGGAGAGTCAGCCCAGCCCCAGAAAGCTAATTGGTGCAGGGAGACCACCTGTCAGGCTGGGAGGCGGGGCCTACAGCCAGGCTGCCGACTCAGGTAAGCCTTAAAGGGGACAAATATGATTCCACGTTTAAGAACGACAGAGTAGGGTGATATATTTGTTAAAACTCAGATCAGGATTCTGTGGCCCAAGGAAGAGTTTTAGTTTTGCCTCCTGATAAGGGATCTGATGAATGTAAAAAGTCATACAGAGCTAATTATGATAATAGCTGCAGTCATTAAGGGCTTGCTACATGCTAGCTAAACCCTTCAGGTAAACACTTCACATTTATTACCTTCTTTTAATCTTAATAACAGTCACTTCGGAGAGGCTGGTTAGGAGCCCAAGGTCACAAAAGTTGATGTCAGGTTTAAGTTCAATCCAGGTCTGTCTTGACCTCAAATTTCTATAACTCTGAAGATCCCAGGAAAGGAATTGGGCGGTGGATCTGAAAGAAGCCAGACAGTGGAGCCTTCAGCCCAGAGGAGGAAGAGAGCAGATGCCCGGGGTTTGCCTCCCAGGGGCAGGGTTTCCAAGCCAGGGCCCTCAGCGCTGGCCTTGAACTGCCAGTGTGGGGTTGGGGATTCCTGGGGAAAGGGATCTGCGGTGAGGTCCCAATCCCATATCCATCTGGGGGCGGGGACCCTGAGGCAGCTACCACTCCTCCACGCTGATCCCAGCCTTCCCTTCTTCCAAG
Seq C2 exon
AGCCAGACCTGGAGGACTGCAGCTTCCGGTGTCGGGGGACCTCCCCTCAGGAGAGTCTGTCTTCCAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000108292-MLLT6:NM_005937:12
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.284 A=NA C2=0.696
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
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
- Autistic and control brains
- Pre-implantation embryo development
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)