HsaEX0038926 @ hg19
Exon Skipping
Gene
ENSG00000138382 | METTL5
Description
methyltransferase like 5 [Source:HGNC Symbol;Acc:25006]
Coordinates
chr2:170668967-170677783:-
Coord C1 exon
chr2:170677602-170677783
Coord A exon
chr2:170676071-170676153
Coord C2 exon
chr2:170668967-170669016
Length
83 bp
Sequences
Splice sites
3' ss Seq
TTTTTTTCTACTCTTCACAGGGA
3' ss Score
9.97
5' ss Seq
GAAGTAAGT
5' ss Score
9.82
Exon sequences
Seq C1 exon
GTTGTGTGTTGGATTTGACATAGATGAAGACGCATTGGAAATATTTAATAGGAATGCAGAAGAGTTTGAGTTAACAAATATTGACATGGTTCAATGTGATGTGTGCTTATTATCTAACAGAATGTCCAAGTCATTCGATACAGTAATTATGAATCCTCCCTTTGGGACCAAAAATAATAAAG
Seq A exon
GGACAGATATGGCTTTTCTAAAGACTGCTTTGGAAATGGCAAGAACAGCAGTATATTCCTTACACAAATCCTCAACTAGAGAA
Seq C2 exon
AACTTCGATATGACCTGCCAGCATCATACAAGTTTCACAAAAAGAAATCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000138382_MULTIEX1-3/4=2-C2
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF051759=MTS=PU(51.1=97.8)
A:
PF063258=PrmA=PD(18.9=37.0)
C2:
PF051759=MTS=FE(12.9=100)
Other Inclusion Isoforms:
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGGAATGCAGAAGAGTTTGAGT
R:
AACTTGTATGATGCTGGCAGGT
Band lengths:
167-250
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)