HsaEX0014675 @ hg38
Exon Skipping
Gene
ENSG00000119397 | CNTRL
Description
centriolin [Source:HGNC Symbol;Acc:HGNC:1858]
Coordinates
chr9:121157740-121159019:+
Coord C1 exon
chr9:121157740-121157880
Coord A exon
chr9:121157983-121158109
Coord C2 exon
chr9:121158855-121159019
Length
127 bp
Sequences
Splice sites
3' ss Seq
GTGTTGCTGGTGCTTTGTAGGCT
3' ss Score
7.54
5' ss Seq
CAGGTATGG
5' ss Score
9.99
Exon sequences
Seq C1 exon
ATCGCTCCAGGCTGATGCAAAGGATTTGGAGCAGCACAAAATCAAGCAAGAAGAAATCTTGAAAGAAATAAACAAAATTGTAGCAGCAAAAGACTCAGACTTCCAATGTTTAAGCAAGAAGAAGGAAAAACTGACAGAAGA
Seq A exon
GCTTCAGAAACTACAGAAAGACATAGAGATGGCAGAACGCAATGAGGATCACCACCTGCAGGTCCTTAAAGAATCTGAGGTGCTTCTTCAGGCCAAAAGAGCCGAGCTGGAAAAGCTGAAAAGCCAG
Seq C2 exon
GTGACAAGTCAGCAGCAGGAGATGGCTGTCTTGGACAGGCAGTTAGGGCATAAAAAGGAGGAGCTGCATCTACTCCAAGGAAGCATGGTCCAGGCAAAAGCTGACCTCCAGGAAGCTCTGAGACTGGGAGAGACTGAAGTAACTGAGAAGTGCAATCACATTAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000119397-'59-71,'59-68,62-71
Average complexity
C1
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.080 A=0.347 C2=0.109
Domain overlap (PFAM):
C1:
PF041027=SlyX=PU(70.8=95.8),PF079267=TPR_MLP1_2=PU(16.8=41.7)
A:
PF041027=SlyX=PD(27.7=41.9),PF079267=TPR_MLP1_2=FE(35.3=100)
C2:
PF079267=TPR_MLP1_2=PD(60.8=87.3),PF140101=PEPcase_2=PU(47.2=90.9)
Main Skipping Isoform:
NA
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:
TGCAAAGGATTTGGAGCAGCA
R:
GTCTCAGAGCTTCCTGGAGGT
Band lengths:
250-377
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