Special

HsaINT1028150 @ hg38

Intron Retention

Gene
ENSG00000204469 | PRRC2A
Description
proline rich coiled-coil 2A [Source:HGNC Symbol;Acc:HGNC:13918]
Coordinates
chr6:31627765-31629334:+
Coord C1 exon
chr6:31627765-31628239
Coord A exon
chr6:31628240-31629143
Coord C2 exon
chr6:31629144-31629334
Length
904 bp
Sequences
Splice sites
5' ss Seq
CAGGTATGG
5' ss Score
9.99
3' ss Seq
TTGTGTTTTTTCCGATGCAGTGG
3' ss Score
7.69
Exon sequences
Seq C1 exon
GATCGTGGGGGTCCTCCCTGCAAGCCCCCAGCACCTGAAGATGAGGATGAGGCATGGCGGCAGCGACGAAAGCAGTCGTCATCTGAGATTTCCCTGGCAGTGGAGCGGGCCCGGCGACGGCGAGAAGAAGAGGAGCGGCGCATGCAAGAAGAGCGCCGGGCAGCCTGTGCTGAGAAGCTCAAGCGACTCGATGAAAAGTTTGGGGCACCTGACAAGCGGCTCAAAGCAGAGCCTGCTGCCCCACCTGCTGCCCCTTCTACCCCAGCTCCACCACCTGCAGTCCCTAAAGAACTCCCTGCACCTCCAGCTCCACCTCCAGCATCAGCCCCAACACCAGAGACAGAACCTGAAGAGCCAGCACAGGCCCCTCCTGCCCAATCTACTCCTACTCCAGGTGTGGCTGCGGCTCCCACTCTGGTGAGTGGTGGTGGCAGTACCAGTAGCACCAGCAGTGGCAGCTTCGAAGCCAGCCCAG
Seq A exon
GTATGGAGATGGGGATAGGTACTACCAGATGTCAGATCACTGCTTCAAGGTGCTTAAAGGTGCAGGGTGGTAAGGCTGGGGATAAATGAAGTAGAAGGCAGTTGTTTTGGTTTATTGGACTATCAGTGATAGTGTTCTATCATTTGTATATCTGAAGGAGGGAAGGTTTTGTCTGGAATCTTAGGTTGTAGTCTAATACCATTTCTTGGCAGAGTACTGTAGCTCACGCCTATAATCCCAACACTTAGGGAGGCTTGGGGTGGAGGATCGCTTGAGCCTAGGGAGTTTGAGACCAGCCTGGGCAACAAAGCAAGACCCTGTCGGCCAGGCATGGTGGCTCACACTTGTAATCCCAGCACTCTGGGAGGCCGAGGCGGGCAGAACATGAGGTCAGGAGTTCAAGATCAGCCTGGCCAACATAGTGAAACCCGTCTCTACTAAAAATACAAAAATTAGCCAAGTGTGGTGGCATGTGCTTGTAGTCCCAGCTGCTTGGGAGGCTGAGGTAGTAGAATCGCTTTAACCCGGGAGGCAGAGATTTCTGTGAGCCAAGACCATGCCATTGCACTCCAGCCTGGGTGACAGAGCAAGACTCTGTCTCAAAAAAAAATCCTGTCTCACAAGAAATACATAAATAAAAATGAAAACTATTTCCTATAGGCCAAGACTGAAGAAAGTACTGTTGTTCTAATGGTTTCATAGAAAGTTAATGCCACCACCATAGGCTCATGAGAGGCCATGAAGTGCTTTAATGGGTCTTAAATGGGAGGGGCTTCAATAGAATAGATGTTGAATAGAATATTTTAGTCTTAAGGGAGCTAGAGATGAGACGTGAGATTCCTGGGGTGTTCATGGAGTGTCTATTGTTGGACTAGATCACTCTGTTGTGTTTTTTCCGATGCAG
Seq C2 exon
TGGAACCACAACTGCCCTCAAAAGAGGGTCCTGAACCACCAGAAGAGGTTCCTCCTCCTACCACACCCCCAGTTCCAAAGGTGGAACCCAAGGGTGATGGGATTGGTCCCACCCGCCAGCCCCCTAGTCAGGGCTTGGGCTACCCCAAATATCAGAAGTCGTTGCCTCCTCGTTTCCAGCGGCAGCAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204469:ENST00000376007:12
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=1.000 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
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ACCACCTGCAGTCCCTAAAGA
R:
GTAGCCCAAGCCCTGACTAGG
Band lengths:
349-1253
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains