Special

HsaEX0027032 @ hg38

Exon Skipping

Gene
ENSG00000136895 | GARNL3
Description
GTPase activating Rap/RanGAP domain like 3 [Source:HGNC Symbol;Acc:HGNC:25425]
Coordinates
chr9:127342219-127349035:+
Coord C1 exon
chr9:127342219-127342334
Coord A exon
chr9:127344235-127344339
Coord C2 exon
chr9:127348924-127349035
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
CCGTGGGAGCCCCAGTGTTTCTGCAGTAATTTCCCTCATGAAGCCGTGTGTGCAGATCCCTGGGGCCAGGCCTTGCTGGTTTCCACTGATGCTGGCGTCTTGCTAGTGGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000136895_MULTIEX3-1/5=C1-3
Average complexity
C2
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.085 A=0.381 C2=0.000
Domain overlap (PFAM):

C1:
PF0214510=Rap_GAP=PD(14.9=71.8)
A:
NO
C2:
PF0078017=CNH=PU(7.2=57.9)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Inclusion Isoforms:


Other Skipping Isoforms:
NA
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
ATTAATGGTGAAAAAGCCACTTTGGA
R:
CATCCACTAGCAAGACGCCAG
Band lengths:
226-331
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