Special

HsaINT0101832 @ hg19

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Coordinates
chr1:3413552-3413925:-
Coord C1 exon
chr1:3413797-3413925
Coord A exon
chr1:3413684-3413796
Coord C2 exon
chr1:3413552-3413683
Length
113 bp
Sequences
Splice sites
5' ss Seq
AGGGTAGGT
5' ss Score
8.1
3' ss Seq
CCCTGCCTGTCTCCACCCAGCCT
3' ss Score
7.84
Exon sequences
Seq C1 exon
CCTGCCTGCGGGGCTGGTTTGGAGAGGCCTGTGCCCAGCGCTGCAGCTGCCCGCCTGGCGCTGCCTGCCACCACGTCACTGGGGCCTGCCGCTGTCCCCCTGGCTTCACTGGCTCCGGCTGCGAGCAGG
Seq A exon
GTAGGTGCTCCCAAGCCCCCACCCCGAGGAGCGGCTGGGCAGGGGGAATCCAGAGAGGCTGCCTGTTCCTTGGCGGGGCTGGGCCAGGACCGACCCTGCCTGTCTCCACCCAG
Seq C2 exon
CCTGCCCACCCGGCAGCTTTGGGGAGGACTGTGCGCAGATGTGCCAGTGTCCCGGTGAGAACCCGGCCTGCCACCCTGCCACCGGGACCTGCTCATGTGCTGCTGGCTACCACGGCCCCAGCTGCCAGCAAC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591-MEGF6:NM_001409:27
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.051 A=NA C2=0.244
Domain overlap (PFAM):

C1:
PF0005319=Laminin_EGF=PU(63.0=65.9)
A:
NA
C2:
PF0005319=Laminin_EGF=PD(30.2=28.9),PF0005319=Laminin_EGF=PU(63.8=66.7)


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:
GGCTGGTTTGGAGAGGCCT
R:
CAGCTGGGGCCGTGGTAG
Band lengths:
242-355
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