HsaEX0059541 @ hg38
Exon Skipping
Gene
ENSG00000169507 | SLC38A11
Description
solute carrier family 38 member 11 [Source:HGNC Symbol;Acc:HGNC:26836]
Coordinates
chr2:164939450-164945727:-
Coord C1 exon
chr2:164945593-164945727
Coord A exon
chr2:164944569-164944634
Coord C2 exon
chr2:164939450-164939556
Length
66 bp
Sequences
Splice sites
3' ss Seq
TATTTTAATTATGTTTTTAGCAA
3' ss Score
5.45
5' ss Seq
GAGGTAAGC
5' ss Score
9.85
Exon sequences
Seq C1 exon
ACTTTTCCCTTGTTTTATTGATAAAAGGAGGGGCCCTCTCTGGAACAGATACCTACCAGTCTTTGGTCAATAAAACTTTCGGCTTTCCAGGGTATCTGCTCCTCTCTGTTCTTCAGTTTTTGTATCCTTTTATAG
Seq A exon
CAATGATAAGTTACAATATAATAGCTGGAGATACTTTGAGCAAAGTTTTTCAAAGAATCCCAGGAG
Seq C2 exon
TTGATCCTGAAAACGTGTTTATTGGTCGCCACTTCATTATTGGACTTTCCACAGTTACCTTTACTCTGCCTTTATCCTTGTACCGAAATATAGCAAAGCTTGGAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000169507_MULTIEX1-5/5=4-C2
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (No Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF0149013=Aa_trans=FE(13.2=100)
A:
PF0149013=Aa_trans=FE(17.5=100)
C2:
PF0149013=Aa_trans=FE(10.2=100)
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AAACTTTCGGCTTTCCAGGGT
R:
TCCAAGCTTTGCTATATTTCGGT
Band lengths:
167-233
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- The Cancer Genome Atlas (TCGA)
- Genotype-Tissue Expression Project (GTEx)
- Autistic and control brains
- Pre-implantation embryo development