HsaINT0033519 @ hg19
Intron Retention
Gene
ENSG00000119397 | CEP110
Description
centriolin [Source:HGNC Symbol;Acc:1858]
Coordinates
chr9:123935953-123937502:+
Coord C1 exon
chr9:123935953-123936015
Coord A exon
chr9:123936016-123937295
Coord C2 exon
chr9:123937296-123937502
Length
1280 bp
Sequences
Splice sites
5' ss Seq
AAGGTTGCC
5' ss Score
-1.7
3' ss Seq
AGTCTTATCACACTTTTCAGGCC
3' ss Score
5.7
Exon sequences
Seq C1 exon
GATGAACACTGGCGTGGAGAAGCACTCCGGGAGAAACTGCGTCACCGGGAAGACCGACTCAAG
Seq A exon
GTTGCCCTTTAAAACAAACAAAAAATCAGTATGAGATACTGGGCACATTGGGGAGGGGAGGGGAAAGTTACATTTACCTGATGCTTTCACATCCATGCTGTTGCAGCCCTGCCAGCAGTGTCAGGGATGGCATGTCTGAAGCTTCGAGGAGTTGGTGTCACACAGTAAATGGCAATCAGTGTTCAAAACCATGACTTCTTGTGTTGACTCCAGTGTTCTTTAACCTATGTAATGCTGCTTTACCTCAGCTAGAACCGATAGAATCTAAGTATTTGGGAGAGGAAGTAGAAACACAGTGATGAACTGTAAGGTTATCATAGGCCAGTGGTGGCAGGAAAGATTTGGGATACTGGAAAAGTAGGCTGAATGTCAGGTAAGGAATTGTTTGGCTCAGAACATGTTGACTTTGAAGGCCTTGTGAGATATCCAGGGAAGGATATCTGTCTGTAGGCAGCCAAAAATAGGAGTCTAGGATTACTGATCAGTGTTGACCTAAAGATTTGAGAGTTAAGAGTATAGGTGGGAGGTTACATTTATGTGGGGGGAATGGCTATGTAGACAGCATGGGATGAGAGAGTGCAGTGCTATAGTATTGAGTGGAGCCCTGTGATGTCCAACAATAGTCTCCAGCCATGTGTGGTTATTTAAATTTTAATAAATTATAATTAAGTTAAAAATTCAGTTATTCATTTGCCACATTTCAAGTGCTTAATAGCCACATGTGTCTAGTGGCTTCTATATTTATAGCCAGAGGTAGAACATTCCCATCATTGCAGAAAGTTCTGTTGGACAGCGCTGCTATAGACTTTGAGAGAATAATTTGATTATAGCAGGGGCAAAAGCCAAAAAGTAGTATGAAGTTGAGGATTAAATACCTAATCATTTATAGACAAGAAACTAAGACTTAGGAAAAAATACATAATCAGGAGACACTCCAGTTGTCAAGTATAAACTGATCTTCTCAGTCATAACAGAAAAGGAAAAAAGAGATGAGGCAATAATTTAATGGAGAAGCAAGGGATACAGAAATCCTAAGCACTGCTAGCATGGAAAAACTGGGCCAAGTGAAAGACCCCGTTAATGACAACACAGAAAAGTAAAGGTTTATGCACACTAAGTATCCACCTGGCACCTCCTACAATTCTTTTTAAAGATGAGCATTTTTGACAGCCATTCCTACTGTTAGCCAGATTTGCCTATCAAATGTATGTGAGGAAGCTGAGCGGCAGTTCTGGTACATTTCTTCTGTGTAAAACCCTAAGTCTTATCACACTTTTCAG
Seq C2 exon
GCCCAACTCCGACACTGTATGTCCAAGCAAGCAGAAGTATTAATTAAAGGAAAGCGGCAGACAGAGGGCACTTTACACAGTTTGAGGAGACAAGTAGATGCTTTAGGGGAATTGGTCACCAGCACCTCTGCAGATTCAGCGTCATCACCCAGTCTGTCTCAGCTGGAGTCTTCCCTCACAGAGGACTCTCAACTTGGACAAAATCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000119397-CEP110:NM_007018:40
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.476 A=NA C2=0.739
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:
GATGAACACTGGCGTGGAGAA
R:
CTGATTTTGTCCAAGTTGAGAGTCC
Band lengths:
270-1550
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- 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)