Special

HsaINT0174147 @ hg19

Intron Retention

Gene
ENSG00000168026 | TTC21A
Description
tetratricopeptide repeat domain 21A [Source:HGNC Symbol;Acc:30761]
Coordinates
chr3:39166554-39167023:+
Coord C1 exon
chr3:39166554-39166651
Coord A exon
chr3:39166652-39166822
Coord C2 exon
chr3:39166823-39167023
Length
171 bp
Sequences
Splice sites
5' ss Seq
GAGGTCAGA
5' ss Score
5.24
3' ss Seq
CTCGGTCCTCTCTTCCACAGGTG
3' ss Score
12.29
Exon sequences
Seq C1 exon
GGATCATCTTGTGTCATATCTTAGAAGGCCACCTGGAGGAAGCTGAGTACCGGCTGGAATTCCTGAAGGAGGTGCAGAAGTCCCTTGGGAAGTCTGAG
Seq A exon
GTCAGAGCTCCCTGGGGGTATGGGTTGCTCCAGGATGATGTCCTCTGCTGTCCTCCCACCCCCACTTTCCAATAGAAAGCATGCAAGGTGGTCTGGACCTTCACTTTGCCCTTGCCTACCAAATCTGCCCAGGCTGACATTGGCACTGAGACTCGGTCCTCTCTTCCACAG
Seq C2 exon
GTGCTAATTTTCCTCCAAGCCCTCCTGATGTCCAGGAAGCACAAGGGGGAGGAAGAGACCACAGCGCTCCTGAAGGAGGCAGTGGAGCTTCACTTCTCCAGCATGCAAGGCATCCCTCTTGGCTCTGAGTACTTTGAAAAGCTGGACCCGTACTTCCTGGTCTGCATTGCTAAGGAGTACTTGCTCTTCTGCCCCAAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000168026-TTC21A:NM_145755:10
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=0.000
Domain overlap (PFAM):

C1:
PF134141=TPR_11=PD(40.6=84.8)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCTGAGTACCGGCTGGAATTC
R:
TGGGGCAGAAGAGCAAGTACT
Band lengths:
253-424
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains