Special

HsaINT0119408 @ hg38

Intron Retention

Gene
ENSG00000070756 | PABPC1
Description
poly(A) binding protein cytoplasmic 1 [Source:HGNC Symbol;Acc:HGNC:8554]
Coordinates
chr8:100713087-100715601:-
Coord C1 exon
chr8:100715462-100715601
Coord A exon
chr8:100713182-100715461
Coord C2 exon
chr8:100713087-100713181
Length
2280 bp
Sequences
Splice sites
5' ss Seq
TTGGTAATG
5' ss Score
4.83
3' ss Seq
TATGTAAAAAAATTTTTTAGGGC
3' ss Score
6.18
Exon sequences
Seq C1 exon
ATTTGTTGGACGATTTAAGTCTCGTAAAGAACGAGAAGCTGAACTTGGAGCTAGGGCAAAAGAATTCACCAATGTTTACATCAAGAATTTTGGAGAAGACATGGATGATGAGCGCCTTAAGGATCTCTTTGGCAAGTTTG
Seq A exon
GTAATGTGTCTTAATTAAATTTTTACACACAAAGCTCTGAATTAGTGCTCAGTGTTAATTTTAGCTATTACTTTATACTAAAAAAGTCAATAAAATTAGACTTACATGGTACTTTAAAATATTTGTGGTTATTTGAATTAAGCTGCTGGCCATCTATTACACTACAAAGTAGTATAATGCAAATAAATAGAATTCTATCCAGGTTAAAGGTTAATAGCATTAGATTAGCACAGTAAGGTATGACTAAGTAATTAGAACAGATTTTAAAATATTTTACTACATTAAGAGGCTGGAGATATATATGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTGTAATTAGAGATCCCATGTCATCAGAAGCATATATTTGACACAGCCAGCCTACAGTGGAATGCAGTCTCATAGAACAATAAAGCTGGTCAGTCTAAGTAACATCATGTTTGAGCAGTTTAAAACAATGACTTTCAGCGATGAAACCAAAAATTCAGATTTTCCAGTGATTCAAAGTACTTATTTCCTGCATTTAAAAATAACTTCATAAAACTTGAAATTGATGAAGCACAAACCAGCCTTAGTTTAGGTAGGGGTATAACAGATAAAATAACTTTTAAGTGTTCATGTGCAGATGATTTGCTTGACCCCACCCTTTGCATTTTGTGTTGAACTTAGAGGTGTCTTGCTTTTTTTAATATGTCAAATAATAAAGAATTAGGAAATCTAATACTTTTTTTTTTGACTCTTGCTCTGTCACCCGGGCTGGAGTGCAGTCACGTGATCTCGGCTCATTGTAGCCTCCGCCTCCCGGGTTCAAGCAGTTCTCCTATCTCTACCTTGAGTAGCTGGGATTACAGGTGTGCGCCACCATGCCCAGCTAATTTTTGTATTTTTATTAGAGACGGGGTTTCACCGTGATGGCCAGGCTGGTCTCCAACTCCTGACCTCAAGTGATCCAGCCACCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACTGTGCCTGGCCAGGAAATCTAATATCTTACTGCCATGCTAGCATGTCACATCAAGCCCTCCACTAGAGCAAAAAAGTACCATTTTGCACAAAGATAGATGATATAAAACATAGAAAGTGACATCATGTTTACATCTCAACCCCCAAATTTAGCTACTGCCTTTTATATATTTCAACTGTCATGCTTCTTAATGTCTTATAATTAGAAGCTGTTTGTAAAAGTTGATGTTAACTACCTACCGTATGAGTAATGCTGCATAAGTTGACCACAAATATGTGAATATGTCATATTTTCTTGACTTTGGCCTCAGGAGAGAGGCACATTCAGAAGAAAATCTGCCTTGGCCCATACATCTTCTAAATTTCTGTAATCAAATGTGATTTTTAACCTTTTCTGCCCCACTTGCCTGAGATACCACCCGCCTCAGTTACCTGTCTCTCCTACTTTAGAGGGAGTTAGGGGAAAACATGTCTTCAGAAATAAATGCTTCCTCTTCCAGGTAGTTCACCTGTGTCTTTAAAAAGAATTTTTTTTCCCTGTCTTTCAAATTCCTGTATTACCTATGTCTTACCAAAGAGTCCAACTATGTATTCCTTCCACTCCTGTTGAAAGTCGGGTAGGCCAAGGCTTAATAAATACTTGTTTCTTAATTGATACAAAGAAAATCAAATTGGTCTTAGCACAATAGCTCATGCCTGTAACCCTAGCGCTTGGGGAGGTCAAAGAGGGAAGATACTTGAAGCCACAAGTTTTAGACTAGCCCGGGCAACATAGCAAGACCCTATCTCTACAAAAAATAAATTAGCCAGGCATGGTGGTATGTGGGCCAGTAGTCCCAGATACTTGGTAAGTTGAGGCAGGAGGATCACTTGAGCCCAGGAGTTGAGTTAAAGTGAGCTTATTCATTGTGCTGCTACACTTCAGCCTGGGCAATGGAATGATATACTGTCTCTATAGAAAAGGGAAAAAATCAAATTATTGGGTAAAAAATGCAACTCTTTTGTGCTAGAGCTGAGAATAAAACTTTTTACAGCCGTTTAAAGTGTACCTCCTTAAATGGAAGGAGGAATCCTTCAGGGGAGGGAAGGTGTTTACCTTCTTAATAATAAAAGGTCTTTCAATGGAAAAGTATACCTACCTGGGGCATAGAAGGCTGGGAGGGAGGAGTCAAGTTACGGAGCTTTGAAATTTTTTTCATGGCTTTGTATGTTGAAATTTGAAATGTATAACGTGAATGTTGTATGGAATATCTTTGATTTATGTAAAAAAATTTTTTAG
Seq C2 exon
GGCCTGCCTTAAGTGTGAAAGTAATGACTGATGAAAGTGGAAAATCCAAAGGATTTGGATTTGTAAGCTTTGAAAGGCATGAAGATGCACAGAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000070756:ENST00000318607:4
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
Associated events
Other assemblies
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