Special

HsaEX0052282 @ hg38

Exon Skipping

Gene
ENSG00000136237 | RAPGEF5
Description
Rap guanine nucleotide exchange factor 5 [Source:HGNC Symbol;Acc:HGNC:16862]
Coordinates
chr7:22125604-22136125:-
Coord C1 exon
chr7:22136038-22136125
Coord A exon
chr7:22131037-22131101
Coord C2 exon
chr7:22125604-22125658
Length
65 bp
Sequences
Splice sites
3' ss Seq
TTTTTGTTTTTAATTTTCAGATG
3' ss Score
11.57
5' ss Seq
CTGGTACGT
5' ss Score
9.57
Exon sequences
Seq C1 exon
GATCCTTCCCTAAATCACAAAGCCTACAGAGATGCATTCAAAAAGATGAAGCCACCAAAAATCCCTTTCATGCCCTTATTGCTTAAAG
Seq A exon
ATGTAACATTTATTCATGAAGGAAATAAAACTTTTTTGGATAATCTTGTCAATTTTGAAAAGCTG
Seq C2 exon
CATATGATCGCAGACACTGTCCGAACCCTGAGACACTGCAGGACTAACCAGTTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136237_MULTIEX1-3/3=2-C2
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=0.042
Domain overlap (PFAM):

C1:
PF0061714=RasGEF=FE(15.7=100)
A:
PF0061714=RasGEF=FE(11.4=100)
C2:
PF0061714=RasGEF=PD(0.5=5.3)


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:
GATCCTTCCCTAAATCACAAAGCCT
R:
CAAACTGGTTAGTCCTGCAGTGT
Band lengths:
143-208
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