Special

HsaINT0134348 @ hg19

Intron Retention

Gene
ENSG00000163629 | PTPN13
Description
protein tyrosine phosphatase, non-receptor type 13 (APO-1/CD95 (Fas)-associated phosphatase) [Source:HGNC Symbol;Acc:9646]
Coordinates
chr4:87679831-87680226:+
Coord C1 exon
chr4:87679831-87679938
Coord A exon
chr4:87679939-87680094
Coord C2 exon
chr4:87680095-87680226
Length
156 bp
Sequences
Splice sites
5' ss Seq
CAGGTACTT
5' ss Score
8.17
3' ss Seq
TGGATTGTCTATTTGTACAGGAG
3' ss Score
5.27
Exon sequences
Seq C1 exon
GATTTCAAATTATTGGTGGGGAGAAGATGGGAAGACTGGACCTAGGCATATTTATCAGTTCAGTTGCCCCTGGAGGACCAGCTGACTTGGATGGATGCTTGAAGCCAG
Seq A exon
GTACTTTACATTTTGGTAGTTTTCTAAGTATTTTCTGACAGGCATGAATTTAGGAACTTAGGCCAAACTAAAATAATTGAGAAAGAGATGATATTTCTAAGATTCAGAATAAATGTATCTTTGTTGTTGAAAATACTGGATTGTCTATTTGTACAG
Seq C2 exon
GAGACCGTTTGATATCTGTGAATAGTGTGAGTCTGGAGGGAGTCAGCCACCATGCTGCAATTGAAATTTTGCAAAATGCACCTGAAGATGTGACACTTGTTATCTCTCAGCCAAAAGAAAAGATATCCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000163629-PTPN13:NM_080685:22
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.045 A=NA C2=0.130
Domain overlap (PFAM):

C1:
PF0059519=PDZ=FE(42.9=100)
A:
NA
C2:
PF0059519=PDZ=PD(41.7=77.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAATTATTGGTGGGGAGAAGATGGG
R:
CTTTGGATATCTTTTCTTTTGGCTGA
Band lengths:
234-390
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