Special

HsaINT0135639 @ hg19

Intron Retention

Gene
ENSG00000119943 | PYROXD2
Description
pyridine nucleotide-disulphide oxidoreductase domain 2 [Source:HGNC Symbol;Acc:23517]
Coordinates
chr10:100150767-100152323:-
Coord C1 exon
chr10:100152189-100152323
Coord A exon
chr10:100150840-100152188
Coord C2 exon
chr10:100150767-100150839
Length
1349 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
ATGGAGCCTTCTCCTTCCAGGAG
3' ss Score
7.75
Exon sequences
Seq C1 exon
ACAGTGGCGAAGGTGCAGGTGAACAGTGAAGGCTGTGTTCAAGGAGTTGTGCTGGAAGATGGCACAGAGGTGAGAAGCAAAATGGTGCTGTCCAACACATCACCGCAGATCACCTTCCTGAAGCTGACGCCACAG
Seq A exon
GTGAGGCTGTGGGCAGGAGGGTGGAGCTTAGATGTCTGCCAAAACAGGGGTTAGAAATCGTGGGGATTGAGGGAGCCAGGATTGCATCAGGGTGTGAGATGCAAAAGCCAAGTCTCTGCATTTGGGAAACAGGGGGGTAAGGGCAGGTAGCAAACGGGGAAGAAGCCTCACAGGTGGGGAGAAGGGGCCAGAGAGGTGAAGTGACCAAGATTCCGGCCATTGGCAGAGCCAGAGCTAGAACCCAGGTCTGACTTTCAATCTAGAGTTATTTCCACAACTTTCCTACTTTCCTGATTTCTCCCCTCTCACCGCTCTAATTCCATTGTCTTTGTCAATGATCTGTTATATTATCCATGATTATTAATTAATCAATTAACAAAGAGCCACAATACTTCTGGGCATACAACAAGAAATACTGGCACCCAGAACTGGAGACTTCAGTTGATCTTGGTGGATTTCAGCTGCTTAAGGCTTGCTCATGCGTCTGCAGTTGGCTGTGGGTCAGCTTGCCGGCTGCTGATCTTGGCGGGACTCCTTCATGTGCCTGGGAGCTGGCTGGTGGTGGCTGGTCCAGGACCGTTTCTGCTGGGATGACCGGGTGGGGGACTCGGCTATGCTCCATGTGTCTGTCCTCCTCCAGCACGGTAGTCCAGGCATGTTCTCAAGGTCTGGCAAAGGGCAAAAGCAGGCAAGCTCAAGCATGCATGCAAGCATCACATGGTTTGATCTCTTTGCATCCTGTTTGCTAGCATTGGCCAGACCAAGTCTCATGGCCAAGCCTAGAGTCAGAGTGTGAGAGCACTGCAAGGTTACACGGAAGTGGGTGTGCAAACAGGGAGGGGTGAGCTTTGGGGGCAGTTTTTGCAATTGACTTACCCTGTGCTCAAAAGATATGATAACATGTATACGCACATGAAGCTCCTAGCCATTCTTGGGGGCAATTCTTAGGGGCAAAGCACTACTTTTTCTGAGTGATTCCATTACTAAAATTCAACAAACATCAGTAAAAAGAAACTTGTTAAGGCAATTCTGAGATCGTCGAGGCTTCCAAGAGCTTACAGACCAGTAGTGAAAAGAGGCCTGCAAACCACTGACCCCTTTGCAAGCAGGGAGAGGTGCGGACTATTTCACAGTCAGAACTGCTGGCCAAGCGCGGAGGAGGAAGTGGTTAGAGCTGAGTGGGAGGGGATCTAGGAAGGCTTCACAGGGGAGGTGGTTTTGGCTGAGCTTTGAAGGATGAAGAGGATTTCCGGAGGGAGCGACTGAGGGATCTTCCTGAGCAAAGAAAGAAGGCAGCTTCCTTGGGGCCTTGGACATCTGAGGCCTTTCATGGAGCCTTCTCCTTCCAG
Seq C2 exon
GAGTGGCTTCCTGAGGAGTTCCTGGAGAGAATCTCTCAGCTGGACACCCGGTCGCCTGTCACCAAGATCAATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000119943-PYROXD2:NM_032709:10
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.022 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0126619=DAO=PD(35.0=95.6)
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:
ACAGTGGCGAAGGTGCAG
R:
TTGATCTTGGTGACAGGCGAC
Band lengths:
206-1555
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