Special

HsaEX6032230 @ hg19

Exon Skipping

Gene
ENSG00000137962 | ARHGAP29
Description
Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:30207]
Coordinates
chr1:94669486-94671239:-
Coord C1 exon
chr1:94671191-94671239
Coord A exon
chr1:94670617-94670754
Coord C2 exon
chr1:94669486-94669550
Length
138 bp
Sequences
Splice sites
3' ss Seq
CTTGATATTTTTGTTTTCAGGAA
3' ss Score
9.41
5' ss Seq
TGGGTGAGT
5' ss Score
8.73
Exon sequences
Seq C1 exon
TCGTTTGAAAATGTTTCTGTGGAATCAGTGGACTCATCCAGTGAAAAAG
Seq A exon
GAAATTTTTCCCCTTTAGAACTAGACAACGTGCTGTTAAAGAACACTGACTCTATCGAGCTGGCTTTGTCATATGCTAAAACTTGGTCAAAATATACTAAGAACATAGTTTCATGGGTTGAAAAAAAGCTTAACTTGG
Seq C2 exon
AATTGGAGTCCACTAGAAATATGGTCAAGTTGGCAGAGGCAACTAGAACTAACATTGGAATTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137962-'5-6,'5-5,6-6=AN
Average complexity
A_S
Mappability confidence:
100%=100=100%
Protein Impact

Alternative protein isoforms (Ref)

No structure available
Features
Disorder rate (Iupred):
  C1=0.059 A=0.000 C2=0.000
Domain overlap (PFAM):

C1:
NO
A:
NO
C2:
PF083036=tRNA_lig_kinase=PU(6.2=31.8)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TCGTTTGAAAATGTTTCTGTGGA
R:
CAATGTTAGTTCTAGTTGCCTCTGC
Band lengths:
106-244
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains