Special

HsaINT0141243 @ hg38

Intron Retention

Gene
ENSG00000164068 | RNF123
Description
ring finger protein 123 [Source:HGNC Symbol;Acc:HGNC:21148]
Coordinates
chr3:49704984-49705679:+
Coord C1 exon
chr3:49704984-49705182
Coord A exon
chr3:49705183-49705533
Coord C2 exon
chr3:49705534-49705679
Length
351 bp
Sequences
Splice sites
5' ss Seq
ACAGTAGGT
5' ss Score
5.67
3' ss Seq
TTCCCTCCCCAACTCCCCAGTTG
3' ss Score
8.02
Exon sequences
Seq C1 exon
CGCCCCATGCAGGCCCTGGCTGTTGGGGGGCCACTGCCCCTGCCCCGGCCCGGCTGGCTCAGTTCTCCAACTTTGGGCCGAGCCAACCGCTTCCTCAGCACAGCGGCTGTGAGCCTCATGACCCCACGGCGGCCTCTGAGCACCTCGGAGAAAGTGAAGGTCCGCACGCTGAGCGTGGAGCAGAGGACCCGTGAGGACA
Seq A exon
GTAGGTGCTTGGTGGGGTCAGGCAGGTCCCCGAAGGACCCTTCCACAGTGTACAGTCCCCGATCCGGGCAAAGCCAAAATACACCCCATGCCCTCCCAGCCCTGTGGCCTGGCAGCATCCCAGGAGTGCAGGAAGCACACTCCGAGGGCAGGAGATCAATGCCGCAGAAATAGGTCCTGGCACCGCAGGCCTTGCCCTGCACTCCACCCCTACCCCCATGCCCCCATGGGCTCCCCGCGGGTCCCTCCTTGGGCACAGGAATGGGAGAGATGATTTCCTCTCCTGCTGTGAGGCAGGCTCAGGAGAGCCGGGATGGCCCTACCCTTGACCCTTCCCTCCCCAACTCCCCAG
Seq C2 exon
TTGAAGGCAGCCACTGGAATGAGGGCTTGCTGCTGGGGCGGCCCCCCGAGGAGCCTGAGCAGCCCCTCACCGAGAACTCGCTGCTGGAAGTCCTGGATGGGGCGGTCATGATGTACAACCTCAGCGTACACCAGCAGCTGGGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164068:ENST00000327697:23
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.467 A=NA C2=0.492
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:
GCTGGCTCAGTTCTCCAACTT
R:
CAGCTGCTGGTGTACGCTG
Band lengths:
287-638
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