Special

HsaINT0101817 @ hg38

Intron Retention

Gene
Description
multiple EGF like domains 6 [Source:HGNC Symbol;Acc:HGNC:3232]
Coordinates
chr1:3507795-3508689:-
Coord C1 exon
chr1:3508558-3508689
Coord A exon
chr1:3507924-3508557
Coord C2 exon
chr1:3507795-3507923
Length
634 bp
Sequences
Splice sites
5' ss Seq
AGAGTGAGG
5' ss Score
2.6
3' ss Seq
TTCCCTGTCATTCTTTGTAGCTT
3' ss Score
10.04
Exon sequences
Seq C1 exon
TCTGCCTGGATGACTCCTTTGGCCATGACTGCAGCTTGACCTGTGATGACTGCAGGAACGGAGGGACCTGCCTCCTGGGCCTGGATGGCTGTGATTGCCCCGAGGGCTGGACTGGGCTCATCTGCAATGAGA
Seq A exon
GTGAGGCAGCTGGGCAGGGGCTGGGGGCTGGGAAGGGGCCTCTGAGCCCCAAGACCTGGGGACAGCCCTTTGAGCCCATTCAGTTTTACTCCTGCCTGCTGGCCCTGGGCAGGGGGCTCTGTGCAGAGCCATTCATTCATCCATTTGTTAATTCCTTTGATAAACATCCCCTGACTGTCCACTCTATGCCACGCACTGTTCCAGGCAGTAAGGATTCCCTGGGAACAAGCAAGTTAAAGTGTTTGTCCTTCCTAAATATCAGTCTTCACGGTCCAGCAACAAGCAAGCCAGCAAATAACTAAGACAGTGAGGGGTGTCTGCTGAAGGGCAGCCGGCAGGTGGGGTTCCTCTAGCTCAGATGGCCAGGGACCCGTCATAACTGTCAGTGAGGCTCTGCCTGTTTGAAAGAGCTGGTTCAGAAGGAGGAGACTCCTCTCTCTGCTGGTGTTCAGAGAGAGGAGTCAGTGATCAATTAGTGATGTCTGCCATGAGCATGGGCAGGGGTGATGTGGTACAAGTGCCATCATTTTATCTCTAGGCAACTGCTTCTAAACCCAAGCCTCCAACCCTAGGAAGGGGTCTCAGAGTGTCGTGCTGGCTGGTGACCCTGACGCTTCCCTGTCATTCTTTGTAG
Seq C2 exon
CTTGTCCTCCGGACACCTTTGGGAAGAACTGCAGCTTCTCCTGCAGCTGTCAGAATGGTGGGACCTGCGACTCTGTCACGGGGGCCTGCCGCTGCCCCCCGGGTGTCAGTGGAACTAACTGTGAGGATG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000162591:ENST00000294599:10
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=68.2)


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:
CTGCCTGGATGACTCCTTTGG
R:
CACAGTTAGTTCCACTGACACCC
Band lengths:
254-888
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