Special

HsaEX6016770 @ hg38

Exon Skipping

Gene
ENSG00000091428 | RAPGEF4
Description
Rap guanine nucleotide exchange factor 4 [Source:HGNC Symbol;Acc:HGNC:16626]
Coordinates
chr2:172735841-172797613:+
Coord C1 exon
chr2:172735841-172736048
Coord A exon
chr2:172795025-172795167
Coord C2 exon
chr2:172797525-172797613
Length
143 bp
Sequences
Splice sites
3' ss Seq
TGCCTTTTCTCCCTATACAGACC
3' ss Score
10.42
5' ss Seq
CATGTAAGA
5' ss Score
5.58
Exon sequences
Seq C1 exon
GGGCGGGCCTGTCGCAGCCGCGCTGGTCGCCAGGCGTCCGGGAGGAGCGGGGTCCGCGCGGCGGACGAGGCGGGGGCGGAGGCGCAGGCAGAGCGAGCGCGGGAGGTCGCCGCAGCCAGGGACACCGCGCGCCGCCGCTCAACATGGTCGCTGCGCACGCTGCCCATTCTTCCTCCTCTGCCGAGTGGATCGCCTGCCTGGATAAAAG
Seq A exon
ACCACTGGAGCGATCCAGCGAAGATGTGGATATAATCTTCACTCGACTGAAAGAAGTTAAAGCTTTTGAGAAATTTCACCCAAATCTCCTTCATCAGATTTGCTTATGTGGTTATTATGAGAATCTGGAAAAGGGAATAACAT
Seq C2 exon
TATTTCGCCAGGGTGATATTGGAACAAACTGGTATGCTGTCCTGGCAGGGTCTTTGGATGTTAAAGTATCTGAGACCAGCAGTCACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000091428-'1-4,'1-3,5-4=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=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
PF0002724=cNMP_binding=PU(20.0=18.4)
C2:
PF0002724=cNMP_binding=FE(31.5=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CCGCTCAACATGGTCGCTG
R:
TGGTGACTGCTGGTCTCAGAT
Band lengths:
162-305
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains