Special

HsaEX0052792 @ hg19

Exon Skipping

Gene
Description
RNA binding motif, single stranded interacting protein 3 [Source:HGNC Symbol;Acc:13427]
Coordinates
chr3:29322837-29529990:+
Coord C1 exon
chr3:29322837-29323247
Coord A exon
chr3:29476234-29476406
Coord C2 exon
chr3:29529932-29529990
Length
173 bp
Sequences
Splice sites
3' ss Seq
ACAGCTTTTTCTGTTTCCAGCAG
3' ss Score
7.39
5' ss Seq
ACCGTAAGT
5' ss Score
10.43
Exon sequences
Seq C1 exon
ATCACTACAGACAGCCTGGTTAGAGAACAAACTGCCTCATCCCAAGTGGACCCCGGCAGCTGGGGGAAGCCAGGCAAGATCTGGGAAGGCTGTGTGTGGGTGTTTTTTCTACAGATCTCACTCCTCGCCCTTTTTTTTTTTCCTTTGGTGTGTGTTTTTTGTTTTGTTTTGTTTTTTAAAAAAATTCTTGCTGTGTTGGAACTAGCGAGTGGTGGAGTCTCTGAAGCCTCATCAGTCACCGGGACTGTCAGGAATAGTGGTTTAAGAGGAAGCTCGGCCTGGGGCACTATACCCTGTCATCCAGTTCCCTGCCTCGGAGATAAAGATTCCAGCTACATGGGCAAACGCCTGGATCAGCCACAAATGTACCCCCAGTACACTTACTACTATCCTCATTATCTCCAAACCAAG
Seq A exon
CAGTCCTATGCACCAGCTCCCCACCCCATGGCTCCTCCCAGCCCCAGCACAAACAGCAGCAGCAACAACAGCAGCAACAACAGCAGCGGGGAACAGTTGAGTAAAACCAACCTGTACATTCGAGGCCTCCCACCAGGCACCACTGACCAGGACCTAATCAAGCTGTGCCAACC
Seq C2 exon
GTATGGAAAAATTGTATCTACAAAGGCAATTCTTGACAAAAACACAAATCAGTGCAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000144642_MULTIEX1-2/2=1-C2
Average complexity
S*
Mappability confidence:
100%=100=100%
Protein Impact

ORF disruption upon sequence exclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.200 A=0.725 C2=0.000
Domain overlap (PFAM):

C1:
PF072236=DUF1421=PU(25.6=84.0)
A:
PF0007617=RRM_1=PU(30.3=35.1)
C2:
PF072236=DUF1421=PD(2.4=9.5),PF0007617=RRM_1=FE(44.4=100)


Main Inclusion Isoform:


Main Skipping Isoform:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
GGTGGAGTCTCTGAAGCCTCA
R:
TGCACTGATTTGTGTTTTTGTCA
Band lengths:
257-430
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