Special

HsaINT0137361 @ hg19

Intron Retention

Gene
ENSG00000079337 | RAPGEF3
Description
Rap guanine nucleotide exchange factor (GEF) 3 [Source:HGNC Symbol;Acc:16629]
Coordinates
chr12:48141495-48141935:-
Coord C1 exon
chr12:48141857-48141935
Coord A exon
chr12:48141646-48141856
Coord C2 exon
chr12:48141495-48141645
Length
211 bp
Sequences
Splice sites
5' ss Seq
CCAATATCC
5' ss Score
-12.74
3' ss Seq
TTCCCTTGACTGGTGCCCACCTT
3' ss Score
-5.98
Exon sequences
Seq C1 exon
AGACATTCCTCAGCGACTTCCTCCTGACCCACAGGGTCTTCATGCCCAGCGCCCAACTCTGCGCTGCCCTTCTGCACCA
Seq A exon
ATATCCTTCCAGCTCCAGGGGGATGGTGTGCATGGGGATAGGATGGTGCGTGGGGTTGAGAGAAAATCTCACCAGCGTGGCTGTGCTGAGCCCTTTAAATGCCAGCCTGCTGCCAGGCCCAGCTTGCCAGGGGCCCTGGGCATCCTGCCCCTCCTTTGCCTCAGGTGGGTGGCCCTGCTTGGATGTTGTGGTTCCCTTGACTGGTGCCCAC
Seq C2 exon
CTTCCATGTGGAGCCTGCGGGTGGCAGCGAGCAGGAGCGCAGCACCTACGTCTGCAACAAGAGGCAGCAGATCTTGCGGCTGGTCAGCCAGTGGGTGGCCCTGTATGGCTCCATGCTCCACACTGACCCTGTGGCCACCAGCTTCCTCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079337-RAPGEF3:NM_001098531:13
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.081
Domain overlap (PFAM):

C1:
PF0061815=RasGEF_N=FE(23.6=100)
A:
NA
C2:
PF0061815=RasGEF_N=FE(45.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
AGACATTCCTCAGCGACTTCCT
R:
CTGGAGGAAGCTGGTGGCC
Band lengths:
230-441
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