Special

HsaINT0101822 @ hg38

Intron Retention

Gene
Description
multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr1:3501177-3501921:-
Coord C1 exon
chr1:3501796-3501921
Coord A exon
chr1:3501309-3501795
Coord C2 exon
chr1:3501177-3501308
Length
487 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGT
5' ss Score
10.67
3' ss Seq
GCCATGGGGGTGGGCACTAGATT
3' ss Score
-0.54
Exon sequences
Seq C1 exon
AGTGCCCGGTGGGGACGTTTGGCGTGAACTGCTCGAGCTCCTGCTCCTGTGGGGGGGCCCCCTGCCACGGGGTCACGGGGCAGTGCCGGTGTCCGCCGGGGAGGACTGGGGAAGACTGTGAGGCAG
Seq A exon
GTGAGTGTCAGCCGCAGCCCCAGTTCCGCCTCCCCAGGCTGCACGGCTCCAAGCTGGTGGGGCCCTGAACTGTGGGGGCCCCAGCCCTGCGGATCCCAGGCCCGTCTATAGCAGGTGTGAGAGCTCACAGTGCACTCCCCTGGGGTAGGGAGGGGGGGTCTGTGGCTGCCCCACCAAGTTCCTGGGGCTTCCAGGCTGCCCTCTCGGGCTGCTCCCTCTCTGCATGAGGCTCCATCTCTAACGGGCTCGGCTCCTTGTGTTGCCAGCTGAACGGTGCCGGGGGCTGGGGGTCCTCTACTGTGGGTGCGCACCCCGCAGCCTGCAGCCCCAGGAGGTGCCCGGGTCCTCTCCCCTCCCCGGGGCAGGCTGAGATGGTAACAGTGGTTCCACCTCCTCGGCCGTGGCTCCAGGGGCATCGTGCCATGTTATGTTGATGTGTTGAGCAAGGGCAGCTTGGGCACTGACTGGCCATGGGGGTGGGCACTAG
Seq C2 exon
ATTGTCCCGAGGGCCGCTGGGGGCTGGGCTGCCAGGAGATCTGCCCAGCATGCCAGCACGCTGCCCGCTGCGACCCTGAGACCGGAGCCTGCCTGTGCCTCCCTGGCTTCGTCGGCAGCCGCTGCCAGGACG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591:ENST00000294599:15
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:
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:
TTTGGCGTGAACTGCTCGAG
R:
CCGACGAAGCCAGGGAGG
Band lengths:
224-711
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