Special

HsaINT0101830 @ hg19

Intron Retention

Gene
Description
multiple EGF-like-domains 6 [Source:HGNC Symbol;Acc:3232]
Coordinates
chr1:3414935-3415390:-
Coord C1 exon
chr1:3415262-3415390
Coord A exon
chr1:3415064-3415261
Coord C2 exon
chr1:3414935-3415063
Length
198 bp
Sequences
Splice sites
5' ss Seq
AGGGTGAGC
5' ss Score
7.75
3' ss Seq
GCCTGCCTCTGCTCCTGTAGAGT
3' ss Score
8.51
Exon sequences
Seq C1 exon
CCTGCCCTGCCGGCCTGTACGGCGACAACTGTCGGCATTCCTGCCTCTGCCAGAACGGAGGGACCTGTGACCCTGTCTCAGGCCACTGTGCGTGCCCAGAGGGCTGGGCCGGCCTGGCCTGTGAGAAGG
Seq A exon
GTGAGCGCTGGGCGGCAGAGGAGGGACATACCCCAGCATGCTTGGTGCAGCCCCGCCTGCAGGCCTAGGAGGGCTCCCAGGTCAGGGGGCAGCGCCCTGGGGTGTAGGCTTCAGCTCTGCGTGCAGGAAGCATGGGTCAGGGTCTCCTGGGCCCAGGAGGCAGGACCCTCACCCTCGTGCCTGCCTCTGCTCCTGTAG
Seq C2 exon
AGTGCCTCCCCCGGGACGTCAGAGCTGGCTGCCGGCACAGCGGCGGTTGCCTCAACGGGGGCCTGTGTGACCCGCACACGGGCCGCTGCCTCTGCCCAGCCGGCTGGACTGGGGACAAGTGTCAGAGCC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591-MEGF6:NM_001409:25
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:
PF079748=EGF_2=WD(100=70.5)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CCTGTACGGCGACAACTGTC
R:
TCTGACACTTGTCCCCAGTCC
Band lengths:
242-440
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