Special

HsaINT0137004 @ hg19

Intron Retention

Gene
ENSG00000160271 | RALGDS
Description
ral guanine nucleotide dissociation stimulator [Source:HGNC Symbol;Acc:9842]
Coordinates
chr9:135976907-135977526:-
Coord C1 exon
chr9:135977325-135977526
Coord A exon
chr9:135977150-135977324
Coord C2 exon
chr9:135976907-135977149
Length
175 bp
Sequences
Splice sites
5' ss Seq
AAGGTGACT
5' ss Score
6.64
3' ss Seq
GATCTTACCGTCTCCCTCAGTTC
3' ss Score
7.37
Exon sequences
Seq C1 exon
CCGCCAGGCCCCCAGCACTGAGCTCAGTACCAGTGGCAGCTCCCACTCCAAGTCCTGTGACCAGCTCAGGTGTGGCCCCTACCTCAGCAGCGGGGACATCGCTGACGCGCTCAGCGTGCACTCGGCCGGCTCCTCTAGCTCCGACGTGGAGGAGATCAACATCAGCTTCGTCCCGGAGTCTCCTGATGGCCAGGAAAAGAAG
Seq A exon
GTGACTGCCTGCCCTTCTCCCCAATATCCTTTCCCATCTCCCCACTCCAAATCCATGCATGGGGCCAGGAAGCCCTGGATCCTGAACACAGCTTCTAGAAGGTTCCCCATCTGGCAGCTGGCCTGGGGTGCCCCCACAGGGCAGTGGGATCTGCTGATCTTACCGTCTCCCTCAG
Seq C2 exon
TTCTGGGAATCAGCCTCACAGTCATCCCCGGAGACCTCCGGCATCAGCTCAGCCTCCAGCAGCACCTCGTCCTCCTCAGCCTCCACCACGCCCGTGGCTGCCACACGCACCCACAAGCGCTCTGTCTCAGGGCTCTGCAACTCCAGCTCCGCGCTGCCGCTCTACAACCAGCAGGTGGGCGACTGCTGTATCATCCGCGTCAGCCTGGACGTGGACAATGGCAACATGTACAAGAGCATCCTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000160271-RALGDS:NM_006266:15
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.377 A=NA C2=0.478
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
PF0078818=RA=PU(22.7=24.7)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATCAACATCAGCTTCGTCCCG
R:
GATGATACAGCAGTCGCCCAC
Band lengths:
243-418
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development