Special

HsaINT0120108 @ hg19

Intron Retention

Gene
Description
papilin, proteoglycan-like sulfated glycoprotein [Source:HGNC Symbol;Acc:19262]
Coordinates
chr14:73721221-73721726:+
Coord C1 exon
chr14:73721221-73721403
Coord A exon
chr14:73721404-73721584
Coord C2 exon
chr14:73721585-73721726
Length
181 bp
Sequences
Splice sites
5' ss Seq
CTAGTGAGT
5' ss Score
7.43
3' ss Seq
CTCCCACTCGTGGGCCTCAGTGC
3' ss Score
5.85
Exon sequences
Seq C1 exon
TGTTCTGTCAGTTGTGGCGTTGGCGTCCGGAAGCGGAGCGTTACTTGCCGGGGTGAAAGGGGTTCTTTGCTCCATACCGCAGCGTGCTCCTTGGAAGACCGGCCACCTCTGACTGAGCCCTGTGTGCATGAGGACTGCCCCCTCCTCAGTGACCAGGCCTGGCATGTTGGCACCTGGGGTCTA
Seq A exon
GTGAGTGCTCTCCACCCCCACACCTGCTGCCTGACCCTGGTCTCTGGCAGGTGGCTGCACCCGAGCGCCGTCCTTGGACCTGACACGCGCCACTGGGCACCTTCCCCTGCCTCTCTCCATGTGGGTCCCCGCCCCCAGCCTCGCCCTCAGCATCTCTCTCTCTCCCACTCGTGGGCCTCAG
Seq C2 exon
TGCTCCAAGAGCTGCAGCTCGGGCACTCGGAGGCGACAGGTCATCTGTGCCATTGGGCCGCCCAGCCACTGCGGGAGCCTGCAGCACTCCAAGCCTGTGGATGTGGAGCCTTGTAACACGCAGCCCTGTCATCTCCCCCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000100767-PAPLN:NM_173462:12
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=0.250
Domain overlap (PFAM):

C1:
PF0009014=TSP_1=PD(81.8=73.8),PF0009014=TSP_1=PU(13.7=11.5)
A:
NA
C2:
PF0009014=TSP_1=PD(82.4=87.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GGGGTTCTTTGCTCCATACCG
R:
GCGTGTTACAAGGCTCCACAT
Band lengths:
246-427
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development