Special

HsaINT0016677 @ hg38

Intron Retention

Gene
ENSG00000130723 | PRRC2B
Description
proline rich coiled-coil 2B [Source:HGNC Symbol;Acc:HGNC:28121]
Coordinates
chr9:131479252-131481808:+
Coord C1 exon
chr9:131479252-131479393
Coord A exon
chr9:131479394-131481725
Coord C2 exon
chr9:131481726-131481808
Length
2332 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGA
5' ss Score
6.65
3' ss Seq
CTGTCTTCCTCCCCTGGCAGCTC
3' ss Score
11.4
Exon sequences
Seq C1 exon
GTGCCTGTCAAAGGTCGAGGCCTTTCCTCCCGTATTCCTCCTCGATTTGCAAAAAAGCAGAACAACTTATGTCTGGAGCAAGGTGACGTGACCGTGCCTGGCAGCAGCCTGGGCACTGAGATCTGGGAGAGCAGCAGCCAGG
Seq A exon
GTGAGAGTTGGGGGTGTGACCCCAGCTGTGGCACCCAAGGTCACATCACACACTGGGTTTGCTTCTGGGGAGGATCCTGCTTTTGAGCTACGAATATAGATGGAATACAGATGGAGTACCTGTTTGCTGTGTTCCGCTGCTGAGCTAGTCGCTGAATGCCGTCTGAGTGATTTGCTGCTGCAACCCCCAAACGGATACACAATTTTCCTTGCCTAAAATTGGTAGAAGAGCAGAGCATTCATTAGTCTGGTGATCTGGAAAAGGATGGCCCCTTGGGCTTAGATCACACAGTAGTGGGAATGGCCTTCTTTGTTGGTCGTCGTTTTCTCCCACTAACTTATGGAAGAGAAGCAAATGACAGATAGACCAGCCGCAAGAGTTCAGGAGCTCTCTTCTGTGCTGTGCACCCTTTTCTTAACATGGGGAAGGCTCTGGAAACCCCTCCCTGAATGCTCTTCTGGAAAGGCAAACTGAGACCAGAAGACGGTATACGTTACTTCTTAGAACATTTGTTGCCCTGAAAACTTTTTTTTTTTAATTCTATATCAAATGTAATTTTTCTGGGAATTTTTCCTTATAAAATAGAAAACTATTTTCATAGAATAGGTTCTTCTTGAGGTTTAGGTGAGGCAGGGCCCTGCGCTGTTAGCCCAGAGCATGCATAGATGAATAAAAACATGGACATTCGATATTTCACAGCTCAGGCCCATGAGGGGAGCTTGGAGAGGTCACCTAGTGCCAGCTCATTTTTCTGCAAAGCAGCTGAAGCTTCTAGAGGGAAGGGACTTGACTCAGGGACTCCAGGGTCATAGGACAAGCACCCGAGACACTGAGTTCTGGGCCTTGATTCTTTCACTGTTTCCACATAGCTTGTCCTCATGTGCTCGGTGAAAACTTTGGTTCTTGCAAACTACAAAATAACATTCAACATGCCCAGCTTTGATGGAAAGGAAGCACAACCATTTGATAAAACATCAATAACACTACATTTGGTAGTGGCTGAGTGACAGGTGTCATAGTATTGGTGTCCAAAAATGCCCAGGTGCCAGATTGGTTGAGCTGCCAGGTGTGAATCAGATGTGACTCTCAGGTGTGAGTCATCATCCCCTTTTGTCAGATCTTTTACTCCAGAATTCTGCAGGGGCTCATTGGTTTCTCAGACCAGGGGTTGTGTCCAAGGGATGGCTTCAGAGAGCCCTTGGATATTAAAATAGCATGTGAAAGGATTTTTTTTTTTTTTAAAGATGGGGTCTCACTATGTTGCCCAGGCTGGACTTGAACCCCTGGGTTCAAGCAATCCTTCTGCCTCAGCCTCCTGAGTAGCTGGGATTGCAGATATGTGCCCCCACCCCCTGCTAGCATGTCAACTTTTGCATGCATATCTATTTTTCTGGGCTCCGGATCCATGGCCATTCAAAAAGTGGTCTGTGAGCTTAAAAATTTTTAGTAATACCCGCTGGGATCTTTCAAAGACTCTGTAGAAGCCACCAACTTTGGCCAGGAGTGGTGGCTCACACCTATAATCCCAGCAGTTTGGGAGGCCAAGGCTTGAAGATCACTTGAGATCAGGAGTTCAAGACCAGCAACAGAGTGAGACCCTGTCTCTATTGTTTAAAAAAAAAAGAAGGCCAGGCCTGGTGGCTCACGTCTGTAATCCCACCACTTTGGGAGGCTGAGGCAGGCAGATCACCAGGTCAGGAGATCGAGACCATCCTGGCTAACATGGTGAAACCCCGTCGCTCCTAAAAATACAACAACAACAAAAAATTAGCCGGGCGTGGTGGCGGGCACCTATAGTCCCAGCTATTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCAGAGCTTGGCAGTGAGTGGAGATCGCGCCACTGCACTCCAGCCTGGGCGACAGAGCAAGACTCCGTCTCCAAAAAAAAAAAAAAAAAAAAAGAAAGATATATTTTTTAATGTAAAAAAAGAGAAGCTACCAACTTTTAGAAATAGTATAAGTGAAAAGAAGCATGAGCATAGCGGAAATAACGACAGAGAATCCAGATTGGCAGGAGTGAGGGCTCTGCCCTGCTCACTCTCTCCTGTAATCCATGAGATGTTGAGAAACACGTTGGGTGAGGATGTGGAAAGTTGGGTAAGGCTGTCAGACCAGCTCTTCCACGTCAGAGCCGTTCACTGGGTGTCACGGGTAGGGGGCTGGGGTGGCGGGTGCAGGGGAGGCAGGGGAGTTGGATTTCTGCAAGCTGTGCCTGTGCTTGTTCTTTAAGAGCTCATAAACTCTCTAGACGGGTTGCTCTTTGATGCCCTGACTCTGTCTTCCTCCCCTGGCAG
Seq C2 exon
CTCTCCCTGTGCAGGCCCCAGCCAACGACTCCTGGAGGAAAGCTGTCACTGCCTTCAGCAGCACCGAGACTGGCTCTGCGGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000130723:ENST00000405995:18
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.854 A=NA C2=1.000
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
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