Special

HsaINT0134378 @ hg38

Intron Retention

Gene
ENSG00000163629 | PTPN13
Description
protein tyrosine phosphatase, non-receptor type 13 [Source:HGNC Symbol;Acc:HGNC:9646]
Coordinates
chr4:86716530-86717117:+
Coord C1 exon
chr4:86716530-86716625
Coord A exon
chr4:86716626-86717023
Coord C2 exon
chr4:86717024-86717117
Length
398 bp
Sequences
Splice sites
5' ss Seq
AAGGTAGGA
5' ss Score
9.45
3' ss Seq
TCTTTTTCATTCATAATTAGTGA
3' ss Score
5.73
Exon sequences
Seq C1 exon
AACCAGTTCGAAGATACAAAACTTATCATGGTGATGTCTTTAGTACCTCCAGTGAAAGTCCATCTATTATTTCCTCTGAATCAGATTTCAGACAAG
Seq A exon
GTAGGAGGCATCTGAAACAAGCAAACTGTTTTTAAGAAACCACGATTATTATTATTTTCAATAGTGTTCAAATATTAATATAAATTGCCAGAAAGAATAATACTGTATAAAATTGAAAAATTTAAAAAAGCTGCTGGTTACTCAGTAGTAGTATTATAGAAACTAAATAGCAGTTTCTTCAAATAACGATGTAGTCCTTTTCATTACAGAGATAATAATTCATTGTCTTTAAAAGTAACATGATTTACCTCAAAAGAGTTTAATAACATTATGTCATTAATTTTGTTCTGTGGATTAGATTTGTACAACTCTATGTCTGCTAAGTGTTTGAGTTTTAAATGAAATTACTCTCATGTTTCTATCACCTGTGCCATTATTTCTTTTTCATTCATAATTAG
Seq C2 exon
TGAGAAGAAGTGAAGCCTCAAAGAGGTTTGAATCCAGCAGTGGTCTCCCAGGGGTAGATGAAACCTTAAGTCAAGGCCAGTCACAGAGACCGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000163629:ENST00000427191:8
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.576 A=NA C2=0.969
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AACCAGTTCGAAGATACAAAACTT
R:
TCTCTGTGACTGGCCTTGACT
Band lengths:
185-583
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development