Special

HsaINT0137719 @ hg19

Intron Retention

Gene
ENSG00000105122 | RASAL3
Description
RAS protein activator like 3 [Source:HGNC Symbol;Acc:26129]
Coordinates
chr19:15565172-15565704:-
Coord C1 exon
chr19:15565468-15565704
Coord A exon
chr19:15565374-15565467
Coord C2 exon
chr19:15565172-15565373
Length
94 bp
Sequences
Splice sites
5' ss Seq
CCCGTAGGT
5' ss Score
4.85
3' ss Seq
CCAGCCTGGCCCTGATCCAGGTT
3' ss Score
4.16
Exon sequences
Seq C1 exon
CTGGTTCCCTGCGGAGCTGGGCATCGTGTTCTCAAGCTGGCGAGAAGCATGTAAAGAACGTGGCTCTGAGGTGCTGGGCCCCCGACTGGTGTGCGCCTCCCTCTTCCTGCGGCTCCTGTGCCCTGCCATCCTGGCACCCAGCCTCTTTGGTTTGGCACCAGACCATCCAGCACCCGGCCCAGCCCGCACCCTCACACTGATTGCCAAGGTCATCCAGAACCTCGCCAACCGTGCCCC
Seq A exon
GTAGGTGCTGGGAAGCTAGGGGTGGGGGGACCATGCTGGGAGTGTGGGGGTGGCAGGTGCCTGACCTGACCCACCCAGCCTGGCCCTGATCCAG
Seq C2 exon
GTTCGGTGAGAAGGAGGCCTACATGGGCTTCATGAATAGCTTCCTGGAGGAACATGGACCAGCCATGCAATGCTTCCTGGACCAGGTAGCCATGGTGGATGTGGATGCTGCCCCCAGTGGTTACCAGGGCAGTGGTGATCTGGCCCTCCAGTTAGCTGTCCTGCATGCCCAGCTCTGTACAATTTTTGCTGAGCTTGACCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105122-RASAL3:NM_022904:12
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
PF0061614=RasGAP=PD(44.2=95.0)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAAGGTCATCCAGAACCTCGC
R:
AGATCACCACTGCCCTGGTAA
Band lengths:
174-268
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