Special

HsaINT0119422 @ hg38

Intron Retention

Gene
ENSG00000101104 | PABPC1L
Description
poly(A) binding protein cytoplasmic 1 like [Source:HGNC Symbol;Acc:HGNC:15797]
Coordinates
chr20:44918906-44919277:+
Coord C1 exon
chr20:44918906-44919045
Coord A exon
chr20:44919046-44919182
Coord C2 exon
chr20:44919183-44919277
Length
137 bp
Sequences
Splice sites
5' ss Seq
TTGGTGGGT
5' ss Score
4.3
3' ss Seq
GCCAGGTTGGTCCTTTGCAGGGA
3' ss Score
5.84
Exon sequences
Seq C1 exon
CTTTGTGGGTCACTTCAAGTCTCGACGGGAGCGGGAGGCGGAGCTGGGGGCGCGGGCCCTGGAGTTCACCAACATCTACGTGAAGAACCTCCCGGTGGATGTGGACGAGCAAGGCCTGCAGGACCTCTTCTCCCAGTTTG
Seq A exon
GTGGGTGTGTCCCCAAGGGAGCGGGGGGATCACTGTTTTTCCTCTTCCCTTCCAAAGTCTGGTAGGGAGGAGGGGCTCTCCTGGGGTTTCCTGAGGACTTCCCAGACTCCCCTTTGAGCCAGGTTGGTCCTTTGCAG
Seq C2 exon
GGAAAATGCTGAGTGTGAAGGTGATGAGGGACAACAGCGGCCACTCGCGGTGCTTTGGCTTTGTCAACTTTGAGAAGCATGAGGAAGCCCAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101104:ENST00000217073:4
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0007617=RRM_1=PD(1.4=2.1),PF0007617=RRM_1=PU(31.4=45.8)
A:
NA
C2:
PF0007617=RRM_1=FE(44.3=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TTTGTGGGTCACTTCAAGTCTCG
R:
CTTCTGGGCTTCCTCATGCTT
Band lengths:
234-371
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