Special

HsaINT0119414 @ hg38

Intron Retention

Gene
ENSG00000101104 | PABPC1L
Description
poly(A) binding protein cytoplasmic 1 like [Source:HGNC Symbol;Acc:HGNC:15797]
Coordinates
chr20:44910144-44912853:+
Coord C1 exon
chr20:44910144-44910336
Coord A exon
chr20:44910337-44912659
Coord C2 exon
chr20:44912660-44912853
Length
2323 bp
Sequences
Splice sites
5' ss Seq
ACGGTGAGC
5' ss Score
9.44
3' ss Seq
CTCCTCTTCCTTCTGTCCAGCGG
3' ss Score
8.15
Exon sequences
Seq C1 exon
ATGAACGCCAGCGGTTCTGGCTACCCGCTTGCCTCGCTTTACGTGGGCGATCTGCACCCCGACGTGACCGAGGCCATGCTCTATGAGAAGTTCTCTCCCGCCGGCCCCATCCTGTCCATCCGCGTGTGCCGCGATGTAGCCACCCGGCGCTCGCTGGGCTACGCCTACATCAACTTCCAGCAGCCCGCGGACG
Seq A exon
GTGAGCCCCGGGGATGGGGCGGGAGGGGAAGGACCGACGGACAAGCAGGCGGACAGACAGAAGCCGGAACTGGGCCGCTTGCGCTTTCATCTTACACTTTGCAGCCGGGGAAACTGAGGCTCAAAGATAACAGGGCGTTGGCAGAGGCCTGGCCCCTGAGACGGGAATTGGTAATTAGTGTGGTTTACTGCTATTCCTCTACAGAGGAGAGAGATTAGGGTCGAGTGAAAACAGATACAGGCTTTGTGGGGGTGGGGGTGGGGGTCAGGCGGACCAGGGATAGAAGCCCAGCAGCCGTGTGACTCTGGGCAAGTTACTCGACCATTCTGAGCTTCAGATGCGTGTCTGGAAAATGGGGGTCCTAGCTGCCTTATAGAGTGCTTGTGAGGATGAGAGATTCAAAGCACCTGGTGAGGAAGATGCCCAAGGCAACACAGCTGGTGAGCAGGGGAGGCAGGAGAACCCAGCCTTGGGCTCAGGCCTTTCCCAGCGCGACGTGAGATCCACACTGGGCGCCTCTACCTGCACGGGCTCTGAAAAACCGCTGCCTCCAGGCCGCAAGGCCGCTTTCTCAGAGCTGATAGCATTGATTAGAGCTTGTCCGATGAGTTTGCCTGCACTTCTGTTGAGAGTGGAGAGGATGAGTGAGCTTGGGCAAGCCTTCACGCTCTGCACCTTTTCATCTGCAAAATGGGGCTAAGGCGTATTCTCCAATAACATAAAGAATGGAGAACTGCTGTCTATGCATAAAGAATGGTAACTGCTTGTTACCTCGTAAACGCTCTTAAGTGGTAACCTAAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAATAAGGCCAGGCGCAGTGGCTCACGCCTGTAATCCCAGCATCTTAGGAGGCCGAGGTGGGCAGATCACTTGAGGTCAGGAGTTCGAGACCAGCCTGGCCAACATAGCGAAACCCTTTCTCTACTAAAAATACAAAAAATAGCTGGGCATGATGGCGGACGCCTGTAATCCCAACTGCTGGGGAGGCTGAGGCACGAGAATCGCTTGAATCCGGGAGGCAGAGGTTGCAGTGAGCCGAGACTGCGCCATTGCACTCCAGCCCGGGCAACAGAGCGAGACTCCATCTCAACACAAAACAAAACAACAAACAAAAAAGAAACAACAACGAAAATAGTGGCTTTAACATTCTGATGTAAGACTCCAGAAACTCACCCAAAAAATGGCCGGCGTCCACTAGAGGGATCCCTTGCGCCAGGTCGCCTGGGTGAACCTGGTGGTTGCCTGAGTGGGTGGTTTGCTAGGGAAGGGGTTGTTCCGCCGGGCCTGTTCCCCGCCCCTTACTGGGCTGGATTCCTGGGCACTTTTCTGTTTGTTCTGCTTTGCTCCACCTCCTGCCTCTTCCCATCTTCCTCCAAGCCCTGTGAATGAAGTGGGACTCGGCCTGGAAACCGTGCTGCAGAGAGAAGGGTTTTGCCCCAGGTATTTATGATAAGACTAGGTGGAGAATCCGGGCTTCCTGAAACTTGCTCCACTGTGTTCCCCACAGCCCCCTTCCATGTCTCTGCACTAGCAGACTCCCTGAAACAGGTCACGTGTATCACCCAGGAGAGACACAGGCTGCAGCAGTGGCCGGAGGCTGGGCATCGGCTGCTGTTTTGAGACATTATTTTGTGTCAGGCACAAAGTTACAAACAAGGCACTTTTACATACCTTCTTTATTTTTCAGTCCCTCCAACAACCTGGTAGTTGGTAGTATCTCCCTTTGTTAGGTGTGGAAAAGTAGGTAATATTACCATCATTCCCCCTTTACAGGTGAGGAACAGGCTCAGAGAGGTAATGTCCACTTTCCCCAGAGCCGGACTGCTTGAGATCTAACCTCAGCTCTGCCCTGCAGCACCTCTGAGTTTTAATTTCCTCAAAGTGCTGCCACCCCTTGTCATATGGACATTGTTATCCACTCAGTGTACTTTAGAATCCAGAATAGACCTGACGCTGCCACAGACCTTTCATGTTTCTTATTCTCAGTTTTCCCATCTGTAAAATGAGGGGCAGGAATCCATGCTCATGTGGCTGCAGGGAGTTGGTTGAATGAGATCATAACTGGAAGGTTGGGGGAGCACCATACACACTAATTCTCAGCTTATCCTTCCTGAGCCTTTGGGCTCTTATCTCAGTTATTTGGGCTCTTATCTTGGCTTATTGTCTGGGACCCAGACAATGACTTTCTCTTTATTGGCTCCCAGTTAAGCACCTCGAGGGGTGGGTGATCAAGGTAAGAAAATTCCCTAAACTTGCTAATTTCTCTCCTCTTCCTTCTGTCCAG
Seq C2 exon
CGGAGCGGGCACTGGACACAATGAACTTTGAGATGCTCAAAGGCCAGCCTATTCGCATCATGTGGTCCCAGCGAGACCCAGGACTTCGCAAGTCAGGTGTGGGCAACATCTTCATCAAGAACCTGGAGGACTCCATTGACAACAAGGCTTTATATGATACCTTCTCCACCTTTGGGAACATCCTCTCTTGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000101104:ENST00000217073:1
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion (1st CDS intron)

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

C1:
PF0007617=RRM_1=PU(73.2=80.0)
A:
NA
C2:
PF0007617=RRM_1=PD(25.4=27.7),PF0007617=RRM_1=PU(40.6=43.1)


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:
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