Special

HsaINT0101825 @ hg38

Intron Retention

Gene
Description
multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr1:3500633-3501094:-
Coord C1 exon
chr1:3500966-3501094
Coord A exon
chr1:3500765-3500965
Coord C2 exon
chr1:3500633-3500764
Length
201 bp
Sequences
Splice sites
5' ss Seq
GAGGTACGG
5' ss Score
9.4
3' ss Seq
GACCCTGAGTTCTGTTGCAGCCT
3' ss Score
3.72
Exon sequences
Seq C1 exon
TGTGCCCAGCAGGCTGGTATGGTCCCAGCTGCCAGACAAGGTGCTCTTGTGCCAATGATGGGCACTGCCACCCAGCCACCGGACACTGCAGCTGTGCCCCCGGGTGGACCGGCTTTAGCTGCCAGAGAG
Seq A exon
GTACGGGGGCCCTTGGCTTGCCCTTTGTCCAGACATCCCTCCTTTCCTAGCCCCTGGAGAGGCCTCTGCCCAGGGCCCCCGAGGACTAGGGGCTTGCAGGAGGCCTTGCCCCAGTCCTGAGACGCCCCTGTGCCTGACTCGGCTGTGGTGCCCGTGGCCCGCGCTTGGGCCTGCGCCGGGTGACCCTGAGTTCTGTTGCAG
Seq C2 exon
CCTGTGATACTGGGCACTGGGGACCTGACTGCAGCCACCCCTGCAACTGCAGCGCTGGCCACGGGAGCTGTGATGCCATCAGCGGCCTGTGTCTGTGTGAGGCTGGCTACGTGGGCCCGCGGTGCGAGCAGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591:ENST00000294599:17
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:
NO
A:
NA
C2:
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:
CAGCAGGCTGGTATGGTCCC
R:
CACGTAGCCAGCCTCACAC
Band lengths:
236-437
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