HsaEX0052842 @ hg19
Exon Skipping
Gene
ENSG00000056586 | RC3H2
Description
ring finger and CCCH-type domains 2 [Source:HGNC Symbol;Acc:21461]
Coordinates
chr9:125652591-125660389:-
Coord C1 exon
chr9:125659558-125660389
Coord A exon
chr9:125655188-125655305
Coord C2 exon
chr9:125652591-125652824
Length
118 bp
Sequences
Splice sites
3' ss Seq
CCTTTTTTTTTTTTTTTAAGGTA
3' ss Score
12.04
5' ss Seq
AAGGTAAGT
5' ss Score
11
Exon sequences
Seq C1 exon
ACACTATTAAGGTATTGTTTCCAGGCAGAATTTCAGAAATGTAATTAATTCAGCAAATAGGTTTTTTAAAAAAGACATCCAAAGGTTATAAAATTATTTAGAAGTATTTTAGGTCTGAAGCTGTAATAGTTGACTTAAGCAATTAACTCTTCAAAGGTGAATGATGAATATGTGGTTAATTCATACTTTTGTCCATTTCTAGCTTACAAAACACTACACAGCAAAATAATGATCTGCTAGACTGCTAACCCGAGCATCCAGCTTCCACAATGCCTGTGCAGGCAGCTCAATGGACAGAATTTCTGTCCTGTCCAATCTGCTATAATGAATTTGATGAGAATGTGCACAAACCCATCAGTTTAGGTTGTTCACACACTGTTTGCAAGACCTGCTTGAATAAACTTCATCGAAAAGCTTGTCCTTTTGACCAGACTGCCATCAACACAGATATTGATGTACTTCCTGTCAACTTCGCACTTCTCCAGTTAGTTGGAGCCCAG
Seq A exon
GTACCAGATCATCAGTCAATTAAGTTAAGTAATCTAGGTGAGAATAAACACTATGAGGTTGCAAAGAAATGCGTTGAGGATTTGGCACTCTACTTAAAACCACTAAGTGGAGGTAAAG
Seq C2 exon
GTGTAGCTAGCTTGAACCAGAGTGCACTGAGCCGTCCAATGCAAAGGAAACTGGTGACACTTGTAAACTGTCAACTGGTGGAGGAAGAAGGTCGTGTAAGAGCCATGCGAGCAGCTCGTTCCCTTGGAGAAAGAACTGTAACAGAACTGATATTACAGCACCAGAACCCTCAGCAGTTGTCTGCCAATCTATGGGCCGCTGTCAGGGCTCGAGGATGCCAGTTTTTAGGGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000056586_MULTIEX2-1/2=C1-2
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact
ORF disruption upon sequence exclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.000 A=0.000 C2=0.000
Domain overlap (PFAM):
C1:
PF0136316=FYVE=PU(70.2=94.8),PF146341=zf-RING_5=WD(100=55.8)
A:
PF0136316=FYVE=PD(27.9=72.5)
C2:
NO
Main Skipping Isoform:
NA
Other Inclusion Isoforms:
Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CAGGCAGCTCAATGGACAGAA
R:
CAGTGCACTCTGGTTCAAGCT
Band lengths:
251-369
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)