Special

HsaINT0101828 @ hg19

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Coordinates
chr1:3415702-3416280:-
Coord C1 exon
chr1:3416152-3416280
Coord A exon
chr1:3415831-3416151
Coord C2 exon
chr1:3415702-3415830
Length
321 bp
Sequences
Splice sites
5' ss Seq
AGAGTGCGT
5' ss Score
3.85
3' ss Seq
CCAGCCCTCTCCACCTGCAGCCT
3' ss Score
8.68
Exon sequences
Seq C1 exon
CCTGCCCGGCCGGCTTCTTTGGATTGGACTGTCGCAGTGCCTGCAACTGCACCGCCGGAGCTGCCTGTGATGCCGTGAATGGCTCCTGCCTCTGCCCCGCTGGCCGCCGGGGCCCCCGCTGTGCCGAGA
Seq A exon
GTGCGTGAGGTCCCTGCTCAGCCCGGGGTGCTGCAGGAGGGGGTGCCAGGTCCTCCGTAGGAGACTCCCTCCTGCCACCTGTCCTGAGTGTCTGAAGCTACCAGGCAACCCCCCTGAGAGTGATGCTTTGCTCACTCGGGCCAGAGCGTTGGTCCTTTTTTGTGGCCACTCTGCTGAGTGGGTGGCCTGAGCCAGAGGGAGGGGAGAGTTGGCCATAGCAGCCGAGGGGACCCCGGCAGATCTGCCCAGCTGGCTGTGATCTGCTGCCAACCCCTGGGGTCCTGCCCACCCCTGGCTCTGACCAGCCCTCTCCACCTGCAG
Seq C2 exon
CCTGCCCAGCCCACACCTACGGGCACAATTGCAGCCAGGCCTGTGCCTGCTTTAACGGGGCCTCCTGTGACCCTGTCCACGGGCAGTGCCACTGTGCCCCTGGCTGGATGGGGCCCTCCTGCCTGCAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591-MEGF6:NM_001409:23
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:
NO
A:
NA
C2:
PF126612=hEGF=WD(100=29.5)


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:
CCGGCTTCTTTGGATTGGACT
R:
CAGGAGGGCCCCATCCAG
Band lengths:
241-562
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