Special

HsaINT0166388 @ hg19

Intron Retention

Gene
ENSG00000069702 | TGFBR3
Description
transforming growth factor, beta receptor III [Source:HGNC Symbol;Acc:11774]
Coordinates
chr1:92181793-92182265:-
Coord C1 exon
chr1:92182125-92182265
Coord A exon
chr1:92181952-92182124
Coord C2 exon
chr1:92181793-92181951
Length
173 bp
Sequences
Splice sites
5' ss Seq
GTGGTATGT
5' ss Score
7.64
3' ss Seq
CTGTGGGTTGTTATTTCCAGTTT
3' ss Score
6.75
Exon sequences
Seq C1 exon
ATTGTGATACAGGTTCCAGCCCTTGGGGACAGTAGTGGTTGGCCAGATGGTTATGAAGATCTGGAGTCAGGTGATAATGGATTTCCGGGAGATATGGATGAAGGAGATGCTTCCCTGTTCACCCGACCTGAAATCGTGGTG
Seq A exon
GTATGTGTTTGTTATCAGTAGGGGGTTTGTGGAAAATGCTGTCTATTTTGTTGGCTTTAGTTAGGGACTATCTGAAAATAAAATCAGATGTTAAAAGCCAAAGCTCATGAAGCTACAGGGCCTTCATCCTTCATATGACTGTCATTAATCTTCCTGTGGGTTGTTATTTCCAG
Seq C2 exon
TTTAATTGCAGCCTTCAGCAGGTGAGGAACCCCAGCAGCTTCCAGGAACAGCCCCACGGAAACATCACCTTCAACATGGAGCTATACAACACTGACCTCTTTTTGGTGCCCTCCCAGGGCGTCTTCTCTGTGCCAGAGAATGGACACGTTTATGTTGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000069702-TGFBR3:NM_001195684:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.404 A=NA C2=0.038
Domain overlap (PFAM):

C1:
PF0010018=Zona_pellucida=FE(16.9=100),PF0038616=C1q=PU(0.1=0.0)
A:
NA
C2:
PF0010018=Zona_pellucida=FE(19.1=100),PF0038616=C1q=FE(72.2=100)


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:
TGTGATACAGGTTCCAGCCCT
R:
GGCACCAAAAAGAGGTCAGTGT
Band lengths:
249-422
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains