Special

HsaINT0136501 @ hg19

Intron Retention

Gene
ENSG00000161800 | RACGAP1
Description
Rac GTPase activating protein 1 [Source:HGNC Symbol;Acc:9804]
Coordinates
chr12:50387914-50388292:-
Coord C1 exon
chr12:50388197-50388292
Coord A exon
chr12:50388113-50388196
Coord C2 exon
chr12:50387914-50388112
Length
84 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGA
5' ss Score
10.06
3' ss Seq
AAATGTCATCTTGATAATAGACA
3' ss Score
1.36
Exon sequences
Seq C1 exon
GGAATGCTGGCAGACTTTGTGTCCCAGACTTCTCCAATGATCCCCTCCATTGTTGTGCATTGTGTAAATGAGATTGAGCAAAGAGGTCTGACTGAG
Seq A exon
GTAAGAGTCAACTGTAGGAGATGGTGAATTTGTTATTTGTGTTAATTCGGAGGTTTTTAAATAAAAATGTCATCTTGATAATAG
Seq C2 exon
ACAGGCCTGTATAGGATCTCTGGCTGTGACCGCACAGTAAAAGAGCTGAAAGAGAAATTCCTCAGAGTGAAAACTGTACCCCTCCTCAGCAAAGTGGATGATATCCATGCTATCTGTAGCCTTCTAAAAGACTTTCTTCGAAACCTCAAAGAACCTCTTCTGACCTTTCGCCTTAACAGAGCCTTTATGGAAGCAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000161800-RACGAP1:NM_001126103:13
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=0.000
Domain overlap (PFAM):

C1:
PF0062022=RhoGAP=PU(11.3=53.1),PF047849=DUF547=PU(22.2=68.8)
A:
NA
C2:
PF0062022=RhoGAP=FE(43.7=100),PF047849=DUF547=FE(66.7=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGCAGACTTTGTGTCCCAGAC
R:
TGCTGAGGAGGGGTACAGTTT
Band lengths:
179-263
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