Special

HsaINT0119437 @ hg19

Intron Retention

Gene
ENSG00000090621 | PABPC4
Description
poly(A) binding protein, cytoplasmic 4 (inducible form) [Source:HGNC Symbol;Acc:8557]
Coordinates
chr1:40035267-40035674:-
Coord C1 exon
chr1:40035535-40035674
Coord A exon
chr1:40035362-40035534
Coord C2 exon
chr1:40035267-40035361
Length
173 bp
Sequences
Splice sites
5' ss Seq
TTGGTAAGT
5' ss Score
10.47
3' ss Seq
GTTCTGTCCTTTGGTAATAGGTA
3' ss Score
7.14
Exon sequences
Seq C1 exon
ATTTGTGGGCAGATTCAAGTCTCGCAAAGAGCGGGAAGCTGAGCTTGGAGCCAAAGCCAAGGAATTCACCAATGTTTATATCAAAAACTTTGGGGAAGAGGTGGATGATGAGAGTCTGAAAGAGCTATTCAGTCAGTTTG
Seq A exon
GTAAGTTGGGGTTCCTTGTCTCCTTTCACAGTCTACCAGACCCATCTGTTTTTTCTTAAGAGATGAGGGCACTGCTCCAGAGATTTGCTTCAAGTGAGTTTCCAGAGGGAAGCCTTCTGTTCCTGAGCTGTGCTCAAGATGGTGTTACTAATAGTTCTGTCCTTTGGTAATAG
Seq C2 exon
GTAAGACCCTAAGTGTCAAGGTGATGAGAGATCCCAATGGGAAATCCAAAGGCTTTGGCTTTGTGAGTTACGAAAAACACGAGGATGCCAATAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000090621-PABPC4:NM_001135653:4
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=0.006
Domain overlap (PFAM):

C1:
PF0007617=RRM_1=PD(1.4=2.1),PF0007617=RRM_1=PU(31.4=45.8),PF0227010=TFIIF_beta=FE(28.0=100)
A:
NA
C2:
PF0007617=RRM_1=FE(44.3=100),PF0227010=TFIIF_beta=FE(18.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TTTGTGGGCAGATTCAAGTCTCG
R:
CTTATTGGCATCCTCGTGTTTTTCG
Band lengths:
234-407
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