Special

HsaINT0137383 @ hg38

Intron Retention

Gene
ENSG00000079337 | RAPGEF3
Description
Rap guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:16629]
Coordinates
chr12:47749390-47749817:-
Coord C1 exon
chr12:47749741-47749817
Coord A exon
chr12:47749537-47749740
Coord C2 exon
chr12:47749390-47749536
Length
204 bp
Sequences
Splice sites
5' ss Seq
AAGGTGAGC
5' ss Score
9.6
3' ss Seq
AGACTGAGGCCTGGCTGCAGGGG
3' ss Score
-0.92
Exon sequences
Seq C1 exon
TGTTCAGCCAGGGGGACAAGGGCACTTCGTGGTACATTATCTGGAAGGGATCTGTCAACGTGGTGACCCATGGCAAG
Seq A exon
GTGAGCCCTCCCTCCTCCCCACCCCAGTGCCCTGGGTCCTAACTGCTCCCTGGTCCATGTCCTCATGGGCAGTGCCTTTGTTGATCTACTGCTGCTGACCCCGTGTCTCCTGTGTGGGTTGTTCTCCTGCCGTGGGTCTGTCCTGGCAAGAGCTGGGGGCGGCAGGGGCGGCAGGGGCGGGCTGAGACTGAGGCCTGGCTGCAG
Seq C2 exon
GGGCTGGTGACCACCCTGCATGAGGGAGATGATTTTGGACAGCTGGCTCTGGTGAATGATGCACCCCGGGCAGCCACCATCATCCTGCGAGAAGACAACTGTCATTTCCTGCGTGTGGACAAGCAGGACTTCAACCGTATCATCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079337:ENST00000449771:9
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.011 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF0002724=cNMP_binding=FE(29.4=100)
A:
NA
C2:
PF0002724=cNMP_binding=FE(56.5=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TGTTCAGCCAGGGGGACAAG
R:
TGATGATACGGTTGAAGTCCTGC
Band lengths:
222-426
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