Special

HsaEX6066158 @ hg38

Exon Skipping

Gene
ENSG00000079337 | RAPGEF3
Description
Rap guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:16629]
Coordinates
chr12:47738022-47738754:-
Coord C1 exon
chr12:47738690-47738754
Coord A exon
chr12:47738193-47738247
Coord C2 exon
chr12:47738022-47738093
Length
55 bp
Sequences
Splice sites
3' ss Seq
TGCCCCGGTGTTGTCCGCAGAGA
3' ss Score
11.26
5' ss Seq
CTGGTGAGA
5' ss Score
7.54
Exon sequences
Seq C1 exon
ACATGACCTTCATTCATGAGGGAAACCACACACTAGTGGAGAATCTCATCAACTTTGAGAAGATG
Seq A exon
AGAATGATGGCCAGAGCCGCGCGGATGCTGCACCACTGCCGAAGCCACAACCCTG
Seq C2 exon
TGCCTCTCTCACCACTCAGAAGCCGAGTTTCCCACCTCCACGAGGACAGCCAGGTGGCGAGGATTTCCACAT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079337-'44-67,'44-66,46-67=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=0.009 C2=0.200
Domain overlap (PFAM):

C1:
PF0061714=RasGEF=FE(11.3=100)
A:
PF0061714=RasGEF=PD(0.5=5.3)
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CACACTAGTGGAGAATCTCATCA
R:
ATGTGGAAATCCTCGCCACCT
Band lengths:
109-164
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains