HsaINT0103677 @ hg19
Intron Retention
Gene
ENSG00000078403 | MLLT10
Description
myeloid/lymphoid or mixed-lineage leukemia (trithorax homolog, Drosophila); translocated to, 10 [Source:HGNC Symbol;Acc:16063]
Coordinates
chr10:22022697-22024164:+
Coord C1 exon
chr10:22022697-22023058
Coord A exon
chr10:22023059-22024067
Coord C2 exon
chr10:22024068-22024164
Length
1009 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGA
5' ss Score
10.77
3' ss Seq
GAATTGTAATCATTTTTCAGTGC
3' ss Score
5.87
Exon sequences
Seq C1 exon
GACTTAACCTCCAGTGGACAAAGTACCAGCAGCTCATCAGCTCTTTCTACCCCACCTCCTGCTGGGCAGAGTCCGGCTCAACAAGGCTCAGGAGTGAGTGGAGTTCAGCAGGTCAATGGCGTGACAGTGGGGGCACTAGCTAGTGGAATGCAGCCTGTAACTTCCACCATTCCTGCCGTGTCTGCAGTGGGTGGAATAATTGGAGCTTTGCCAGGTAACCAACTGGCAATTAATGGCATTGTAGGAGCTTTAAATGGGGTTATGCAGACTCCTGTCACAATGTCCCAGAACCCTACCCCTCTCACCCACACAACCGTACCACCTAATGCAACACATCCAATGCCAGCTACACTGACTAACAG
Seq A exon
GTAAGAAACTTAAGTATGTTTTGGGTTTTTTAGTATAACAGAGTACCGGTGTTGTCTATGCCTTAGATTGGGGCTTTCAATGTGTTCCTTTGTAGATACACCTTAAGAAGTCTGCCAAAAATTTTAAGTATATTATACAGAGTACATTTATTTTTGAAACTTAAGTAATTTAGATTAAAATTAAGTTACTTTTAGTAACAGCATTATGTTCTGTGCTGAAAATTAGTCTTAATCTGTGATGTCTGTTTTTAAATACTAGTTTTTCTTATTTCTTTGTATACTGTATCATAAATTCTGAAGAAAGATATCGTAGTGGAGATAACATGAATATTAGTTTCCTAAAATTTATGTAATATTTTTAATGTTCTAATCAAAGATTTTGATATAGGATAAAGGTCATTTATCTGAATTCCCAGGAAGTGAGACTCACTGGTTTCATTGTACTGGAACTGCATTTGAATGTTTGTTCAAAACTAGGGGACTAAAGCTATGTTGTTATTAAGCATACTTTTGGGGGAATAAATACTTTTAAATGGATTTGCAGTGGGTACTAGAAAGCTATTTCCTGTAGCTCTCTTCCTTGGTGTTTAGTTTTACCATTGGGACCATTAGAAAAGGATAGGTCAAATCAGTGGTATGTTTGGATTCTTTGTTTCAAATATGTGTTTACTTAGTGTGAGTTAAATTATCCTTGAATAATTAAAGATAAATTATTACATACGCTTGTTAGAAACACATGTAAATTTCTATTCCATAAAATGAGTTAGGGCCTATTTGTTTTATAATAAAAACATTTCTTGACAATGTGAATTCTTGTTTAGCTGTACACATGGATGTATATAAACATACATATATATAGAAATTGTACATAACTGTTTTCAGAGTGTTTGGATTCAGAATTGTACTTAAGTTATTAAACATCAAATTGAAAAGTTGTCTTTCATTTTTAGACTTCTAAAAATGCATTAGAGGTGTGTAGTAAAAAGTAAGAATTGTAATCATTTTTCAG
Seq C2 exon
TGCCTCAGGACTAGGATTACTTTCTGACCAGCAACGACAAATACTTATTCATCAACAGCAGTTTCAGCAGTTGTTAAATTCTCAACAGCTCACACCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078403-MLLT10:NM_004641:21
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.587 A=NA C2=0.293
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
NO
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TTTCTACCCCACCTCCTGCTG
R:
TGTCGTTGCTGGTCAGAAAGT
Band lengths:
358-1367
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)