HsaINT0119416 @ hg19
Intron Retention
Gene
ENSG00000101104 | PABPC1L
Description
poly(A) binding protein, cytoplasmic 1-like [Source:HGNC Symbol;Acc:15797]
Coordinates
chr20:43564032-43565371:+
Coord C1 exon
chr20:43564032-43564138
Coord A exon
chr20:43564139-43565277
Coord C2 exon
chr20:43565278-43565371
Length
1139 bp
Sequences
Splice sites
5' ss Seq
CGGGTAAGG
5' ss Score
10.17
3' ss Seq
GTGTCCCCGGCACCATGCAGGTC
3' ss Score
5.24
Exon sequences
Seq C1 exon
CCAACATTGGTACTCAGACCACAGGACCCAGTGGGGTAGGATGCTGTACACCAGGCCGGCCGCTCCTGCCGTGCAAATGTTCCTCAGCAGCACATAGCACCTATCGG
Seq A exon
GTAAGGCCAGCCCAGCTGCCTGCTCTTAGCCTGGGCTCCTGGCCGCCTGGCTCAGAACCTTAGCTAAGGTGTTGGGCCTTGGCTTTTTTTCTTTTCTTGGCTTGTAAAGTTTCGTTTATTAATGTGTACAATCAATAAGAGATCACCCTTACTGCGAGAAGGGGAAAGAGGGCCAGCATTACGTTTTATTTACAATTTGTTTTGCTTCGGTTATTACCAAAATTAATTTGGATATCCTTAGTATTTGTGATGAACACCAAGGAAAGGTATTCTAAGAATATGCTGATTATTGAAGGGATGTACTTAATCTTCAAAACAGAAAATACTTACTGTAATCAAAGACTGTGTATTTATCTCCCTCCCCTAAAAAAGGCCTAAAATTCAGCATTATCATATCCTGTGTAGAATTTCAATGTGTCTCTTTTGAACTATTTCCTGCAAAATGAATGAGAACAGTCTTTAAACAGCAAAAATGTCTATTTTTTTTTTTGGACAGGGTCTTTTTTTTGACAGCACCCAGGTTAGAGTGCAGTGGTGTGATCATAGCTCACTGCAGCCTTGAACTCCTAGGCTCAAGTGATCCTCCCACCTCAGCCTCCAAGTACAGGCATGTGACACCATGCCTGGTTAATTTTGTGTATTTTTTTGTAGTGACAGGGGTCTCATTATGTTGCCAAGGCTGATCTCAAACTCCTGGCCTCAAGCGATCCTCCCACTTTGGCCTTCCAAAGTTCTAGGATTATAGGTGTGAGCCACCACACCTGGCCAAAATGTTTTAAAATTACCAAGATGTGAAAGGGTGAGAGGTGTGCCGGGGACATGTCCATAAATCTACTTGATAAAAAGTGCTTTATTTGGCACAAAGTTATTGGTAACACAGGGCTTTCCTTTATCAACGTTCATCAGGGACCTTTATAAGTTCGTAGCACTACAGGAAACGTCTAAGCTAGAGGCATGACTTTGTCTTCTAATCCACTTTGCCCTTGTTGGGGACTCTCCACCCCACCTGATCATCCAGACCTTGCCCTCTGTTCCCCTCCTCCAGTGCCTCCCTGGCCTTCTGCTCACTTGCCAGGGTAAGTATTTTGAGGACATGCCTGTCCATGGTGATTAAGGGATGTGTCCCCGGCACCATGCAG
Seq C2 exon
GTCCAGGAGCCGGCTGTGCACATCCCAGGACAGGAGCCCCTGACCGCGTCCATGCTGGCTGCGGCGCCCCTGCATGAGCAAAAGCAGATGATTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101104-PABPC1L:NM_001124756:11
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.347 A=NA C2=0.391
Domain overlap (PFAM):
C1:
NO
A:
NA
C2:
PF0065813=PABP=PU(29.0=62.5)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
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
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)