Special

HsaINT0114896 @ hg38

Intron Retention

Gene
ENSG00000074181 | NOTCH3
Description
notch 3 [Source:HGNC Symbol;Acc:HGNC:7883]
Coordinates
chr19:15170086-15170553:-
Coord C1 exon
chr19:15170331-15170553
Coord A exon
chr19:15170171-15170330
Coord C2 exon
chr19:15170086-15170170
Length
160 bp
Sequences
Splice sites
5' ss Seq
GAAGTGAGA
5' ss Score
3.22
3' ss Seq
CTCTTCCCATTGTCCGCCAGGAA
3' ss Score
9.28
Exon sequences
Seq C1 exon
GGGAGCCGCTGGAGCCTCCAGAACCCAGCGTCCCGCTGCTGCCACTGCTAGTGGCGGGCGCTGTCTTGCTGCTGGTCATTCTCGTCCTGGGTGTCATGGTGGCCCGGCGCAAGCGCGAGCACAGCACCCTCTGGTTCCCTGAGGGCTTCTCACTGCACAAGGACGTGGCCTCTGGTCACAAGGGCCGGCGGGAACCCGTGGGCCAGGACGCGCTGGGCATGAA
Seq A exon
GTGAGAACCCTGCTCGCTCCCTGTCCCTGACTACGGGGACCTTGTGAACCCTGGACCCCGCCTTGACCTGACTCAGACCTCTGACCCCACCCCAAATCCTCCTTCCCAGCTGGACACCTCTAGTGTCCCCCTCACATCCCCTCTTCCCATTGTCCGCCAG
Seq C2 exon
GAACATGGCCAAGGGTGAGAGCCTGATGGGGGAGGTGGCCACAGACTGGATGGACACAGAGTGCCCAGAGGCCAAGCGGCTAAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000074181:ENST00000263388:27
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.347 A=NA C2=0.587
Domain overlap (PFAM):

C1:
PF076847=NODP=PD(13.8=12.0)
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:
TGGAGCCTCCAGAACCCAG
R:
CCCATCAGGCTCTCACCCTT
Band lengths:
244-404
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