Special

HsaEX0027032 @ hg19

Exon Skipping

Gene
ENSG00000136895 | GARNL3
Description
GTPase activating Rap/RanGAP domain-like 3 [Source:HGNC Symbol;Acc:25425]
Coordinates
chr9:130104498-130107756:+
Coord C1 exon
chr9:130104498-130104613
Coord A exon
chr9:130106514-130106618
Coord C2 exon
chr9:130107682-130107756
Length
105 bp
Sequences
Splice sites
3' ss Seq
AACTTGTTTTTCTTTTTTAGAAC
3' ss Score
10.74
5' ss Seq
CAGGTGGGT
5' ss Score
8.56
Exon sequences
Seq C1 exon
TAATTAATGGTGAAAAAGCCACTTTGGAAACCCCAACATTTGCCCAGAAACGTCGGCGTACCCTGGATATGTTGATTAGATCTTTACACCAGGATTTGATGCCAGATTTGCATAAG
Seq A exon
AACATGCTTAATAGACGATCTTTTAGTGATGTCTTACCAGAGTCACCCAAGTCAGCGCGGAAGAAAGAGGAGGCCCGCCAGGCGGAGTTTGTTAGAATAGGGCAG
Seq C2 exon
GCACTAAAACTGAAATCCATTGTGAGAGGGGATGCTCCATCAAGCTTGGCAGCTTCAGGGATCTGTAAAAAAGAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136895-'34-36,'34-35,35-36
Average complexity
S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.077 A=0.343 C2=0.000
Domain overlap (PFAM):

C1:
PF0214510=Rap_GAP=PD(14.9=71.8)
A:
NO
C2:
NO


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AATTAATGGTGAAAAAGCCACTTTGG
R:
TTTTTACAGATCCCTGAAGCTGCC
Band lengths:
186-291
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • The Cancer Genome Atlas (TCGA)
  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development