Special

HsaEX0052100 @ hg38

Exon Skipping

Gene
ENSG00000116191 | RALGPS2
Description
Ral GEF with PH domain and SH3 binding motif 2 [Source:HGNC Symbol;Acc:HGNC:30279]
Coordinates
chr1:178893919-178902211:+
Coord C1 exon
chr1:178893919-178894024
Coord A exon
chr1:178897664-178897756
Coord C2 exon
chr1:178902106-178902211
Length
93 bp
Sequences
Splice sites
3' ss Seq
CCTGTGTTTGTCCTATCCAGGTA
3' ss Score
11.07
5' ss Seq
CATGTAAGT
5' ss Score
8.31
Exon sequences
Seq C1 exon
TTCTGCAGAATCAGAAGATTTGGCAGTACATTTATATCCAGGAGCTGTTACTATTCAAGGTGTTCTCAGGAGAAAAACTTTGTTAAAAGAAGGCAAAAAGCCTACA
Seq A exon
GTAGCATCTTGGACAAAATATTGGGCAGCTTTGTGTGGGACACAGCTTTTTTACTATGCTGCCAAATCTCTAAAGGCTACCGAAAGAAAACAT
Seq C2 exon
TTCAAATCAACATCCAATAAGAACGTATCTGTGATAGGATGGATGGTGATGATGGCTGATGACCCTGAACATCCTGATCTCTTCCTGCTGACTGACTCTGAGAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000116191_CASSETTE3
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (No Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.011 C2=0.000
Domain overlap (PFAM):

C1:
PF154131=PH_11=PU(24.3=47.2)
A:
PF154131=PH_11=FE(44.3=100)
C2:
PF154131=PH_11=PD(30.0=58.3)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGCAGAATCAGAAGATTTGGCAGT
R:
GGGTCATCAGCCATCATCACC
Band lengths:
168-261
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