Special

HsaINT0146217 @ hg19

Intron Retention

Gene
ENSG00000146197 | SCUBE3
Description
signal peptide, CUB domain, EGF-like 3 [Source:HGNC Symbol;Acc:13655]
Coordinates
chr6:35208918-35209436:+
Coord C1 exon
chr6:35208918-35209043
Coord A exon
chr6:35209044-35209319
Coord C2 exon
chr6:35209320-35209436
Length
276 bp
Sequences
Splice sites
5' ss Seq
CAGGTGGGC
5' ss Score
8.07
3' ss Seq
GGCCTCTCTCCCCTTCCTAGAGC
3' ss Score
9.1
Exon sequences
Seq C1 exon
ATGTGGATGAATGCAGCATCAACCGGGGAGGTTGCCGCTTTGGCTGCATCAACACTCCTGGCAGCTACCAGTGTACCTGCCCAGCAGGCCAGGGTCGGCTGCACTGGAATGGCAAAGATTGCACAG
Seq A exon
GTGGGCAGTGCCCTCTGCTGGCCAAAGATGACACTGCCATTTCAGGGAGCAGTTGGGGTTCTGGAAAGCATAGAGTATCACATTGGGGAAAGGTGTGAGGTGGAAAGGGTGGAGAATGTAGCCATTTTGAGTTAAAGACATGAAATTTGTAGTAAACAATCCCATCATCAGTCTCCATGGGTACAACAATAGTTATGCAAGTAGCTGATTCCTCCAAATTACCCAACTGAGGGAAAGGAATGCATTCATTTGCTCAGGCCTCTCTCCCCTTCCTAG
Seq C2 exon
AGCCACTGAAGTGTCAGGGCAGTCCTGGGGCCTCGAAAGCCATGCTCAGCTGCAACCGGTCTGGCAAGAAGGACACCTGTGCCCTGACCTGTCCCTCCAGGGCCCGATTTTTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000146197-SCUBE3:NM_152753:10
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:
PF146701=FXa_inhibition=WD(100=86.0)
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:
GGATGAATGCAGCATCAACCG
R:
GCAAAAATCGGGCCCTGGAG
Band lengths:
236-512
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