HsaINT0174149 @ hg19
Intron Retention
Gene
ENSG00000168026 | TTC21A
Description
tetratricopeptide repeat domain 21A [Source:HGNC Symbol;Acc:30761]
Coordinates
chr3:39169825-39170423:+
Coord C1 exon
chr3:39169825-39169979
Coord A exon
chr3:39169980-39170207
Coord C2 exon
chr3:39170208-39170423
Length
228 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
3' ss Seq
CTCTGCTGTGCTCCTCCTAGGTC
3' ss Score
10.17
Exon sequences
Seq C1 exon
AGCTAGAGAATGCCCAGAGCATCCTGCAGCGTTGCCTGGAGCTGGACCCCGCCTCCGTGGATGCCCATCTCCTCATGTGTCAGATCTACTTGGCTCAGGGCAACTTTGGCATGTGCTTCCACTGCTTAGAGCTGGGTGTCAGCCACAACTTCCAG
Seq A exon
GTGGGTGCCCTCTCATCCTCTCAGCATCCCAAAGCCCAGCTAGCTGTGGCCCCTGTTTGCCTTCTGAGAGTAGCCCCAGGGGCTAGCTGTGTCCCGTAGATCTTTCTGCTCGTCCAAAGGCAGGGGTAGGCTCAGTGGGCTCCTGAGGCTTTCTCTGACCTGGCTGCTGTGAGCAGCAGCAGTAGCAGCAGTGAACTGGAGCCCCACACTCTGCTGTGCTCCTCCTAG
Seq C2 exon
GTCCGAGATCACCCCCTCTACCACCTCATCAAGGCCAGGGCCCTCAACAAGGCTGGAGACTATCCAGAGGCCATAAAGACGCTGAAAATGGTCATCAAATTGCCAGCTCTGAAGAAGGAAGAAGGCAGAAAGTTCCTCAGGCCCTCTGTGCAGCCTAGCCAGCGGGCATCCATCTTATTGGAACTGGTGGAGGCCCTCCGGCTGAATGGGGAGCTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000168026-TTC21A:NM_145755:13
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=NA C2=0.014
Domain overlap (PFAM):
C1:
PF128952=Apc3=FE(60.0=100)
A:
NA
C2:
PF128952=Apc3=PD(35.3=41.7)
Main Inclusion Isoform:
NA

Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGGATGCCCATCTCCTCATGT
R:
GGGCCTCCACCAGTTCCAATA
Band lengths:
294-522
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)