Special

HsaINT0101827 @ hg38

Intron Retention

Gene
Description
multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr1:3499588-3499924:-
Coord C1 exon
chr1:3499796-3499924
Coord A exon
chr1:3499717-3499795
Coord C2 exon
chr1:3499588-3499716
Length
79 bp
Sequences
Splice sites
5' ss Seq
ATGGTGAGC
5' ss Score
8.27
3' ss Seq
TCACTGCCCGCTGTCTGCAGCCT
3' ss Score
8.42
Exon sequences
Seq C1 exon
AGTGTCCCCAGGGCCACTTTGGGCCCGGCTGTGAGCAGCGGTGCCAGTGTCAGCATGGAGCAGCCTGTGACCACGTCAGCGGGGCCTGCACCTGCCCGGCCGGCTGGAGGGGCACCTTCTGCGAGCATG
Seq A exon
GTGAGCTACGGCACAGGCGGGGGCTAGGCTGGGTGGCCTCCAGTGTGGGCCCCTCCACATCACTGCCCGCTGTCTGCAG
Seq C2 exon
CCTGCCCGGCCGGCTTCTTTGGATTGGACTGTCGCAGTGCCTGCAACTGCACCGCCGGAGCTGCCTGTGATGCCGTGAATGGCTCCTGCCTCTGCCCCGCTGGCCGCCGGGGCCCCCGCTGTGCCGAGA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591:ENST00000294599:19
Average complexity
IR
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:
PF0005319=Laminin_EGF=PD(34.0=36.4)
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:
GTGCCAGTGTCAGCATGGAG
R:
ATTCACGGCATCACAGGCAG
Band lengths:
169-248
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