Special

HsaINT0128605 @ hg19

Intron Retention

Gene
ENSG00000130653 | PNPLA7
Description
patatin-like phospholipase domain containing 7 [Source:HGNC Symbol;Acc:24768]
Coordinates
chr9:140387465-140389598:-
Coord C1 exon
chr9:140389485-140389598
Coord A exon
chr9:140387535-140389484
Coord C2 exon
chr9:140387465-140387534
Length
1950 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGC
5' ss Score
9.6
3' ss Seq
GCTCCTGTGTCTGCCCGCAGGTG
3' ss Score
12.66
Exon sequences
Seq C1 exon
GTGGAGACACTGACCCACCAGGCCCGGGCGACCACGGTGCATGCCGTTCGGGACTCAGAATTGGCCAAGCTGCCGGCAGGAGCCCTCACGTCCATCAAGCGCAGGTACCCACAG
Seq A exon
GTGAGCATGGCGTGGGTGAGGATGCGGAGCGGATGAGGGTGTGGAGTGGATGAGGGCATGGAACAGGTGAGGGCGGAGCGGGTGAGGGCACAGAGCAGGTGAGGGCGCGGAGCAGGTGAGAGCGCAGAGCAGGTGAAGGCGCGGAGTGGATGAGGTCACGGAGCAGGTGAGGGCAGGGCGCAGGTGAGGGTGCAGAGTGGATGAGGTCACGGAGCAGGTGAGGGCAGGGCGCAGGTGAGGGTGCGGAGTGGATGAGGTCACGGAGCAGGTGAGGGCAGGGCGCAGGTGAGGGTGCGGAGCTGGTGAGGGCGCAGAGCAGGTGAAGGCACAGAGTGGATGAGGTCATGGAGCAGGTGAGGGCAGGGCACAGGTGAGGGCGCGGAGCAGGTGAGGGTGCGGAGTGGATGAGGTCACGGAGCAGGTGAGGGCAGGGCGCAGGTGAGGGTGCGGAGCAGGTGAGGGCGCAGAGCAGGTGAGGGCGCGGGTGAGGGTGGTGCGGGTGAGGGTGGCACAGGCCATGTCCCAAACTGTGCCCTGAGTTGTGGTGATCATTCGGTCTACCTACACATGGATGGAAAACGACCTGGAGGAGGTGAAGATTAGAGCCCAGCTGGGTGGGGGCGGTGACGGTGAGCAGGAAACCTGGAGAGGCGCCCAGGCTGCTTCCCAGGACAGTCGTGCAGCTGCCTTCTTGGTGGCCTCTCTACTCATGAGTGATGTGGGTGTGGCAGAGGAAAGGGAAGTGACTCTCACTCTGAGATCTGGAGAAGGACAGGGCGGGCTGCTCGGAAGTGCAGGGTCAGCGGTGAGGAGAGCGCCCAGGAAGGACCGGCAGAGGGGCCTGAAGGGCAGGTCTGCAGTTGTTCATCAGCCAGCACACGGATCCCAAGAAGTTTTTCATTCTAGAACAAATGGAAAGGGGGTGCAGGTGTGGCCCACAGCATGTTGCAGGGCCTTTTACGGCCAGTGCCTCTCACCACCCCTGGGGCTCATCCTGAGAGGCCACCACTGCCCTCCCTCCACCGCCTCCCCTCAGGTAGCGCTTCTCCCACTCAAAGCTCTTGGGCCATGGTTCTCCTGCCCGCAGCTCCTGGATCCTGGTTCTCCTGCCCGCAGATCCTAGGTCCTGGCGCTTGCTGTACTTGCCCACTTATGGACCAGGAGAGCCTGGCGGAGCATGTGAGTGCAGCTCACAGGGCCAGCAGGCTCCAGGGTGGCAGCCACAGTTGCTGGGAACAGCAGGGAGCCAGGCCACTCCTCCATCTTTGTCCTGGCCTGCAGGGTGGGCCTCGTTCTCATGAGCGCCTCGGAGCAGGAGCCCTGGCCCACCCTTTAGAGGCCGCTGCAGGGCTCCATCCAACCAGCAGCTTCTGGGGGACAGTGCGGGTGAAGCCAGTGGGTCCGCTGTTGTGGGGCCAGCTTTGCTGTACAGTCAGCCCCTGGGCAGGGTCCCTGCAAGCCAGCAACCCCTGGTGTGGGGACCGTTTGGTCCAGTCAGGACAAATGTCCCCAACCGTGCCCTGAAGCAGGCTTGGCACCCAGAAGCAACAGCCACAATGAGCCCTCAGTTCCAGAGAAGCCTGCCAGCCTGCCCTTGTCCTGCCTTCAGGGTCGTGGGTGGCTTGCTTGGAGTTGTCTGCCTGCCCTGAAGTGAGAGTGAGAGGCTGGCCTGGGCTCACGGTCACAGAGGACATACCCCTTGTACCTGCTGGCCTGGCAACCAGAAAGGCAGCCGTATGGCTTACCTGGGCATCAAGAAGGCTGCAAGGCCTAAACAGCCATGGCCCAGCACGTGGCTTGTGAGTCATGTGCAACTCAGTTCATGGAGGTTTTGAAAAGCAGATCCAGCGCCATTGGCTGAGTCTCGCTGTTGTTGAGCATCACTGTCTTTGGTTCCCAGTGTTTCTCAGTTTAAAACGTGTGGCTCTTGGCTCCTGTGTCTGCCCGCAG
Seq C2 exon
GTGGTGACTCGGCTGATTCATCTCTTGGGTGAGAAGATCCTGGGCAGCCTCCAGCAGGGACCTGTGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130653-PNPLA7:NM_152286:18
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=0.035
Domain overlap (PFAM):

C1:
PF0002724=cNMP_binding=FE(40.7=100)
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:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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