HsaINT0130411 @ hg19
Intron Retention
Gene
ENSG00000118898 | PPL
Description
periplakin [Source:HGNC Symbol;Acc:9273]
Coordinates
chr16:4947676-4949121:-
Coord C1 exon
chr16:4949014-4949121
Coord A exon
chr16:4947772-4949013
Coord C2 exon
chr16:4947676-4947771
Length
1242 bp
Sequences
Splice sites
5' ss Seq
GAGGTTCAT
5' ss Score
1.75
3' ss Seq
GCCCCTTCTCTTCCTGGCAGGCG
3' ss Score
10.69
Exon sequences
Seq C1 exon
AATTTCATCAACCGGAACCTGGAGGCCAAAGAGGAGAGAATCAACAAACTGCACAGCGAGGGCGACCAGCTGCTGGCGGCCGAGCACCCCGGGAGGAACTCCATTGAG
Seq A exon
GTTCATGCACCCCGAGACCAGACACCTCCCCCAGGGTGGCTTCTGGTTGGCCGCTGCCTGTGGGCCGCCTGGAGCTCGGGCAGACCCCGGAGCTGGGGGTCCTGCAAGCTGCATCTTGTGTCTGTCTGTCTCTTTCTTGCTGTGTCTGACTCTGCCTCCTCCATTTATCCTGATCCGTTGACACTTCTGCCCTCAGCCCCTGGACTTCTGAAGCCCCTGTGGGGTCTGTATTAGTTTCCTAGAGTTGCTGCAACAAGTTAAAACAAACTTAGTGGCTTTAAACAACAGAAATTCATTCTCTCAGAGGTCTGTGGGCTGTAAGTCTGAAATCAAGGTGTCTTAGGGCCTCATTCCCTCTGGAAGCTCCAGGACATGTGCCTTCCTTGCTCTTCCGGCTTCTGGGGGTTGCCAACAGCCCTTGGCTTGTGGCTGCATCATTCCAGTCCCTTCCTCCGTCTTCACATGGCCTTCTCTCCCCATGTCTCTCTGTATCCTCTCTTCTTATAAGGATATCAGTCAGTGGATTTAGGGCTCACCCTAATTTCAGGATCCTTAACTAATGACATCTGCAAAGATCTTATTCCCAAATAAGGTCGCATTCTTCCCAACCCCCACAATGCCACCAACCCCGCCTGAGATGGAGTTTCGCTGTTGTTGCCCAGGCTGGAGTGCGATGGTGTAATCTTGGCTCACTGCAACCTCCACCTCCCGGGTTCAAGCAATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCGCACACCATCATGCCCAGCTAATTTTTGTATTTTTAGTAGAGACAGGGTCTCATCATGTGGGCCAGGCTAGTCTCAAACTCCTGACCTCAGGTGATCCACCCGCCTCGGCCTCCCAAAGTGCTGCGATTACAGGTGTGAGCCACCATGCCTGGCCAGGGTCATGGATTTGGTGGGACACTGTTCGGTCCATGACAGTGCCTTTGTACAGATTTGCCGAAGGCACCACAGCCCCCACTTGCCCTTTGTGCACTGCACAGCCTGGGCATCCGTATGTGGCATCCCTGTTTGGCTCCTTGACGTGACCCCTCTCTCCTCCTCCCACTCCTGAGCAGAAGCTGGCTACCCCTGTGGTAGCCACACCCAGACAGATGCCAGATGCCTCCCTCCCCCGCCATGCCCCAGCCCAATATCCCAGCAGTCCCTCCCTTGGTGTCTGCAGTACCTGCCCAGTGGTGACCGGCCCCTTCTCTTCCTGGCAG
Seq C2 exon
GCGCACATGGAGGCTGTGCACGCAGACTGGAAGGAGTACCTGAACCTGCTCATCTGCGAGGAGAGCCACCTCAAGTACATGGAGGACTACCACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000118898-PPL:NM_002705:8
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.500 A=NA C2=0.031
Domain overlap (PFAM):
C1:
PF0043516=Spectrin=FE(33.7=100),PF123293=TMF_DNA_bd=PU(91.7=91.7)
A:
NA
C2:
PF0043516=Spectrin=PD(22.1=71.9),PF123293=TMF_DNA_bd=PD(2.8=3.1),PF0043516=Spectrin=PU(5.1=12.5)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TCATCAACCGGAACCTGGAGG
R:
GGTGGTAGTCCTCCATGTACT
Band lengths:
198-1440
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)