HsaEX6004899 @ hg19
Exon Skipping
Gene
ENSG00000177103 | DSCAML1
Description
Down syndrome cell adhesion molecule like 1 [Source:HGNC Symbol;Acc:14656]
Coordinates
chr11:117387182-117392120:-
Coord C1 exon
chr11:117391845-117392120
Coord A exon
chr11:117389181-117389477
Coord C2 exon
chr11:117387182-117387454
Length
297 bp
Sequences
Splice sites
3' ss Seq
GGGCTTCTCGCTCCCTGCAGATG
3' ss Score
11
5' ss Seq
GAGGTGCCT
5' ss Score
4.01
Exon sequences
Seq C1 exon
ATCCCCTTCATGTGACCCTGACACCAAAGAAGCTGAAGACCGGCATTGGCAGCACGGTCATCCTCTCCTGTGCCCTGACGGGCTCCCCAGAGTTCACCATCCGCTGGTATCGCAACACGGAGCTGGTGCTGCCTGACGAGGCCATCTCCATCCGCGGGCTCAGCAACGAGACGCTGCTCATCACCTCGGCCCAGAAGAGCCATTCCGGGGCCTACCAGTGCTTCGCTACCCGCAAGGCCCAGACCGCCCAGGACTTTGCCATCATTGCACTTGAGG
Seq A exon
ATGGCACGCCCCGCATCGTCTCGTCCTTCAGCGAGAAGGTGGTCAACCCCGGGGAGCAGTTCTCACTGATGTGTGCGGCCAAGGGCGCCCCGCCCCCCACGGTCACCTGGGCCCTCGACGATGAGCCCATCGTGCGGGATGGCAGCCACCGCACCAACCAGTACACCATGTCGGACGGCACCACCATCAGCCACATGAACGTCACAGGCCCCCAGATCCGCGACGGGGGCGTGTACCGGTGCACAGCGCGGAACTTGGTGGGCAGTGCTGAATATCAGGCGCGAATAAACGTAAGAG
Seq C2 exon
GCCCACCCAGCATCCGGGCTATGCGGAACATCACAGCAGTCGCCGGGCGGGACACCCTTATCAACTGCAGGGTCATCGGCTATCCCTACTACTCCATCAAGTGGTACAAGGATGCCCTGCTGCTGCCAGACAACCACCGCCAGGTGGTGTTTGAGAATGGGACCCTCAAGCTGACTGACGTGCAGAAGGGCATGGATGAGGGGGAGTACCTGTGCAGTGTCCTCATCCAGCCCCAGCTCTCCATCAGCCAGAGCGTTCACGTAGCCGTCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000177103-'5-6,'5-5,6-6=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact
Alternative protein isoforms (Ref)
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.240 C2=0.000
Domain overlap (PFAM):
C1:
PF0767911=I-set=WD(100=94.6)
A:
PF0767911=I-set=WD(100=95.0)
C2:
PF0767911=I-set=WD(100=96.7)
Main Skipping Isoform:
NA
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
ACCAAAGAAGCTGAAGACCGG
R:
GACTGCTGTGATGTTCCGCAT
Band lengths:
295-592
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
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)