Special

HsaINT0137365 @ hg19

Intron Retention

Gene
ENSG00000079337 | RAPGEF3
Description
Rap guanine nucleotide exchange factor (GEF) 3 [Source:HGNC Symbol;Acc:16629]
Coordinates
chr12:48137313-48137851:-
Coord C1 exon
chr12:48137770-48137851
Coord A exon
chr12:48137460-48137769
Coord C2 exon
chr12:48137313-48137459
Length
310 bp
Sequences
Splice sites
5' ss Seq
AAGGTTGGT
5' ss Score
8.46
3' ss Seq
CAGTCTGGTCTCCTCTTCAGTCC
3' ss Score
5.93
Exon sequences
Seq C1 exon
GCCCGGAACTTGCCTGTTTGGCTCCCCAACCAGGACGAGCCCCTTCCTGGCAGCAGCTGTGCCATCCAAGTTGGGGATAAAG
Seq A exon
GTTGGTGGTCTGTGCCGGCTGGGCACAGCCCGACATCTGCACCCTGCTGTCTCTGCCTCTCTTGTCCTGCTGTCGTCACTCTTGACCTCGGTGTGCCTGGGCCAAGGTGGCACGCTGTACTCCTCAGGGTCTGTGTTCCAGGCTGCTGGCTAGATCTGCCTCCTACCTGCCTCTTTTTTGCTCAGGGCCTCCCCACCTGCAGCTCAGCCTCTTGGGGATCCCTCCCACCATTACTGCAATAGCCGCCCTCTCCCTCCTGGGGTGGAGATCAGGCAGCCCTTCCCACAGCTCAGTCTGGTCTCCTCTTCAG
Seq C2 exon
TCCCCTATGACATCTGCCGGCCAGACCACTCAGTGTTGACCCTGCAGCTGCCTGTGACAGCCTCCGTGAGAGAGGTGATGGCAGCGTTGGCCCAGGAGGATGGCTGGACCAAGGGGCAGGTGCTGGTGAAGGTCAATTCTGCAGGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079337-RAPGEF3:NM_001098531:17
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.250 A=NA C2=0.008
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCCGGAACTTGCCTGTTTGG
R:
ACCTGCAGAATTGACCTTCACC
Band lengths:
227-537
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