Special

HsaINT0096213 @ hg19

Intron Retention

Gene
Description
NA
Coordinates
chr12:57577162-57577692:+
Coord C1 exon
chr12:57577162-57577293
Coord A exon
chr12:57577294-57577557
Coord C2 exon
chr12:57577558-57577692
Length
264 bp
Sequences
Splice sites
5' ss Seq
CTGGTGAGC
5' ss Score
8.05
3' ss Seq
GTCACCTCCTCCACCTCCAGAAA
3' ss Score
9.26
Exon sequences
Seq C1 exon
GCGTAGGTTCCTTTCTCCTGTACTCTGTGCATGAGGGAATCAGGGGAATTCCCCTGGATCCCAATGACAAGTCAGATGCCCTGGTCCCAGTGTCCGGGACCTCGCTGGCTGTCGGCATCGACTTCCACGCTG
Seq A exon
GTGAGCCATTTGGTGGCAGAGGGAGTTGGGCGTGGCGTAGGAGCTTTAGGGGTGGTGTGGTGTGCCCTGAGGGTCCAGTGAGAGGCTGCCTGAATTGGCCTGAGGTGGGGCACTTGCTACAGCTGCCACCCTGACTCCACCTCCCCTTCAAGCACCTGGCCCCTCCGGCACTCTCTCACCTCTGTCTTGAGCCTTGTGAGATTTTGACCCCTCACCTTACCCCTGCCTTATTGGGCATCCCCATGTCACCTCCTCCACCTCCAG
Seq C2 exon
AAAATGACACCATCTACTGGGTGGACATGGGCCTGAGCACGATCAGCCGGGCCAAGCGGGACCAGACGTGGCGTGAAGACGTGGTGACCAATGGCATTGGCCGTGTGGAGGGCATTGCAGTGGACTGGATCGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000242108-LRP1:NM_002332:35
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
NA
A:
NA
C2:
NA


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GCGTAGGTTCCTTTCTCCTGT
R:
GATCCAGTCCACTGCAATGCC
Band lengths:
263-527
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development