Special

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


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
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