Special

HsaALTD0005435-3/3 @ hg19

Alternative 5'ss

Gene
ENSG00000164068 | RNF123
Description
ring finger protein 123 [Source:HGNC Symbol;Acc:21148]
Coordinates
chr3:49742520-49743112:+
Coord C1 exon
chr3:49742520-49742606
Coord A exon
chr3:49742607-49742619
Coord C2 exon
chr3:49742967-49743112
Length
13 bp
Sequences
Splice sites
5' ss Seq
TAGGTGCTT
5' ss Score
1.61
3' ss Seq
TTCCCTCCCCAACTCCCCAGTTG
3' ss Score
8.02
Exon sequences
Seq C1 exon
CGGCTGTGAGCCTCATGACCCCACGGCGGCCTCTGAGCACCTCGGAGAAAGTGAAGGTCCGCACGCTGAGCGTGGAGCAGAGGACCC
Seq A exon
GTGAGGACAGTAG
Seq C2 exon
TTGAAGGCAGCCACTGGAATGAGGGCTTGCTGCTGGGGCGGCCCCCCGAGGAGCCTGAGCAGCCCCTCACCGAGAACTCGCTGCTGGAAGTCCTGGATGGGGCGGTCATGATGTACAACCTCAGCGTACACCAGCAGCTGGGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000164068-27-27,28-27,29-27-3/3
Average complexity
Alt5
Mappability confidence:
NA
Protein Impact

ORF disruption when splice site is used (sequence inclusion)

No structure available
Features
Disorder rate (Iupred):
  C1=0.473 A=NA C2=0.492
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CTGTGAGCCTCATGACCCCA
R:
CATTCCAGTGGCTGCCTTCAA
Band lengths:
105-118
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