Special

HsaINT0011493 @ hg38

Intron Retention

Gene
ENSG00000137962 | ARHGAP29
Description
Rho GTPase activating protein 29 [Source:HGNC Symbol;Acc:HGNC:30207]
Coordinates
chr1:94177612-94178167:-
Coord C1 exon
chr1:94177852-94178167
Coord A exon
chr1:94177721-94177851
Coord C2 exon
chr1:94177612-94177720
Length
131 bp
Sequences
Splice sites
5' ss Seq
GAAGTGAGT
5' ss Score
7.97
3' ss Seq
AAATTATCTTGCATCAACAGGAT
3' ss Score
7.55
Exon sequences
Seq C1 exon
GGTAGTAGATCATGCAGAAGAAAACAAGATGAACTCCAAAAACTTGGGGGTGATATTTGGACCAAGTCTCATTAGGCCAAGGCCCACAACTGCTCCTATCACCATCTCCTCCCTTGCAGAGTATTCAAATCAAGCACGCTTGGTAGAGTTTCTCATTACTTACTCACAGAAGATCTTCGATGGGTCCCTACAACCACAAGATGTTATGTGTAGCATAGGTGTTGTTGATCAAGGCTGTTTTCCAAAGCCTCTGTTATCACCAGAAGAAAGAGACATTGAACGTTCCATGAAGTCACTATTTTTTTCTTCAAAGGAA
Seq A exon
GTGAGTTTGACCTTTATAGAATTATATTAGAACTTTGTAATATTTATGTTAATAAGTTAAAGATCTTTGAACTGTTTATTTTGAGGTTATGTTTTACTTCTTCCATTTTAAAAATTATCTTGCATCAACAG
Seq C2 exon
GATATCCATACTTCAGAGAGTGAAAGCAAAATTTTTGAACGAGCTACATCATTTGAGGAATCAGAACGCAAGCAAAATGCGTTAGGAAAATGTGATGCATGTCTCAGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000137962:ENST00000260526:21
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.019 A=NA C2=0.189
Domain overlap (PFAM):

C1:
PF0062022=RhoGAP=PD(18.3=30.2)
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:
GCACGCTTGGTAGAGTTTCTCA
R:
TGCTTGCGTTCTGATTCCTCA
Band lengths:
257-388
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