Special

HsaINT0137381 @ hg38

Intron Retention

Gene
ENSG00000079337 | RAPGEF3
Description
Rap guanine nucleotide exchange factor 3 [Source:HGNC Symbol;Acc:HGNC:16629]
Coordinates
chr12:47749930-47750425:-
Coord C1 exon
chr12:47750341-47750425
Coord A exon
chr12:47749991-47750340
Coord C2 exon
chr12:47749930-47749990
Length
350 bp
Sequences
Splice sites
5' ss Seq
TCGGTCAGT
5' ss Score
7.03
3' ss Seq
CTCCTATCTCCACCACACAGGTG
3' ss Score
8.06
Exon sequences
Seq C1 exon
CCCAGGTCAGCGCACGGATGAAGAGCTGGACCTCATCTTTGAGGAGCTGCTGCACATCAAGGCTGTGGCCCACCTCTCCAACTCG
Seq A exon
GTCAGTCCTGCCCCTCCCAGCCCTGCCCCGTACCAGGCATCTTCTCTTCCTGTGACTTCCCTGAAACTCCAACTGCTGGGCCAGAGGGCATTTCTCCACTTCCATCTATGGCTGGAAATTTTCAGTCTGATTTCTTGCCCCCGGCGCTGCCCTGTCTGAAAATCCTTCCGCCTCTCTCAGCCCATTTTCTCCACTTGCTTTGTCTCCTGCTGAATCCTGGGAACACCTGACCTGGCCACATCTTTGTCCCCCAGCACTTGTGTCTTTGGACCTAACCACACCCCTAGCAAAAGCCTGGCTGCTCTGCACATGAACTTGTCGCCACCGACTCTCCTATCTCCACCACACAG
Seq C2 exon
GTGAAGCGAGAATTAGCGGCTGTTCTGCTCTTTGAACCACACAGCAAGGCAGGGACCGTGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079337:ENST00000449771:7
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.003 A=NA C2=0.009
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0002724=cNMP_binding=PU(8.2=33.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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