Special

HsaINT0146221 @ hg19

Intron Retention

Gene
ENSG00000146197 | SCUBE3
Description
signal peptide, CUB domain, EGF-like 3 [Source:HGNC Symbol;Acc:13655]
Coordinates
chr6:35210399-35211013:+
Coord C1 exon
chr6:35210399-35210557
Coord A exon
chr6:35210558-35210797
Coord C2 exon
chr6:35210798-35211013
Length
240 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGA
5' ss Score
6.71
3' ss Seq
ACACGGCCATCCACCACCAGCCA
3' ss Score
3.7
Exon sequences
Seq C1 exon
GTGGTGCCCCCTGCTCTGAATGCCAGGTCACCTTCATCCACCTTAAGTGTGACTCCTCTCGGAAGGGCAAGGGCCGACGGGCCCGGACCCCTCCAGGCAAAGAGGTCACAAGGCTCACCCTGGAACTGGAGGCAGAGGTCAGAGCCGAAGAAACCACAG
Seq A exon
GTGGGACTGGGGGCACTGTTGGGAAGAGGACTGGAAGGGGAGGGCAGAGGTGGGGAAACCACAGGTCTCAGCAGCAAAAGGAAGGGATGGAGCCTGTACTAGGGGCAGACCCTGCCTGGTGCCAAGCCTAAAAGCTAGTCCCTCTTACCATGCCCCTCCTAGCTCCCAGCTTTGCTCCCCTGCCCTCCTGCTCACAGCAACTCTTTCTCCTCCCTGATACACACGGCCATCCACCACCAG
Seq C2 exon
CCAGCTGTGGGCTGCCCTGCCTCCGACAGCGAATGGAACGGCGGCTGAAAGGATCCCTGAAGATGCTCAGAAAGTCCATCAACCAGGACCGCTTCCTGCTGCGCCTGGCAGGCCTTGATTATGAGCTGGCCCACAAGCCGGGCCTGGTAGCCGGGGAGCGAGCAGAGCCGATGGAGTCCTGTAGGCCCGGGCAGCACCGTGCTGGGACCAAGTGTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146197-SCUBE3:NM_152753:14
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.444 A=NA C2=0.219
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
AGTGTGACTCCTCTCGGAAGG
R:
TACAGGACTCCATCGGCTCTG
Band lengths:
297-537
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Genotype-Tissue Expression Project (GTEx)
  • Autistic and control brains
  • Pre-implantation embryo development