Special

HsaINT0136503 @ hg19

Intron Retention

Gene
ENSG00000161800 | RACGAP1
Description
Rac GTPase activating protein 1 [Source:HGNC Symbol;Acc:9804]
Coordinates
chr12:50386028-50386438:-
Coord C1 exon
chr12:50386333-50386438
Coord A exon
chr12:50386161-50386332
Coord C2 exon
chr12:50386028-50386160
Length
172 bp
Sequences
Splice sites
5' ss Seq
GAGGTGAGT
5' ss Score
10.03
3' ss Seq
TTTAATATTCTTTTGCTTAGAGT
3' ss Score
6.31
Exon sequences
Seq C1 exon
AAATCACAGATGAAGACAACAGCATAGCTGCCATGTACCAAGCTGTTGGTGAACTGCCCCAGGCCAACAGGGACACATTAGCTTTCCTCATGATTCACTTGCAGAG
Seq A exon
GTGAGTACAGCAGAAACTTGTTCTGGGAGTTAGGGAATTTTTTTCCAAGGGGAAGATAATGTGGGTTGAGTGTTTGGGAGTATGAGGGATGAATTGTTTTCTTATAGAATTTATATTTTGGTCTGCATTTAAGCAAGGAGCAAGACTTCTAATTTAATATTCTTTTGCTTAG
Seq C2 exon
AGTGGCTCAGAGTCCACATACTAAAATGGATGTTGCCAATCTGGCTAAAGTCTTTGGCCCTACAATAGTGGCCCATGCTGTGCCCAATCCAGACCCAGTGACAATGTTACAGGACATCAAGCGTCAACCCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000161800-RACGAP1:NM_001126103:15
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=0.133
Domain overlap (PFAM):

C1:
PF0062022=RhoGAP=FE(23.2=100),PF047849=DUF547=PD(9.1=25.0)
A:
NA
C2:
PF0062022=RhoGAP=PD(20.5=68.9)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
TCACAGATGAAGACAACAGCA
R:
TTGGGTTGACGCTTGATGTCC
Band lengths:
235-407
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