Special

HsaINT0096233 @ hg19

Intron Retention

Gene
Description
NA
Coordinates
chr12:57589441-57589786:+
Coord C1 exon
chr12:57589441-57589563
Coord A exon
chr12:57589564-57589645
Coord C2 exon
chr12:57589646-57589786
Length
82 bp
Sequences
Splice sites
5' ss Seq
GTGGTGAGC
5' ss Score
6.64
3' ss Seq
CAGGTCCATTCCTCCCCCAGAGT
3' ss Score
7.75
Exon sequences
Seq C1 exon
TGTACAACAGCACTTGTGACGACCGTGAGTTCATGTGCCAGAACCGCCAGTGCATCCCCAAGCACTTCGTGTGTGACCACGACCGTGACTGTGCAGATGGCTCTGATGAGTCCCCCGAGTGTG
Seq A exon
GTGAGCCTTCGGCGGTGGTGGGAGGAGGCCCTGCCCTCTGCCGGGCCAGGGCATCAGCCTCACAGGTCCATTCCTCCCCCAG
Seq C2 exon
AGTACCCGACCTGCGGCCCCAGTGAGTTCCGCTGTGCCAATGGGCGCTGTCTGAGCTCCCGCCAGTGGGAGTGTGATGGCGAGAATGACTGCCACGACCAGAGTGACGAGGCTCCCAAGAACCCACACTGCACCAGCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000242108-LRP1:NM_002332:53
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:
CAGTGCATCCCCAAGCACTTC
R:
CTGGTCGTGGCAGTCATTCTC
Band lengths:
177-259
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