Special

HsaINT0114829 @ hg19

Intron Retention

Gene
ENSG00000148400 | NOTCH1
Description
notch 1 [Source:HGNC Symbol;Acc:7881]
Coordinates
chr9:139417302-139418431:-
Coord C1 exon
chr9:139418169-139418431
Coord A exon
chr9:139417641-139418168
Coord C2 exon
chr9:139417302-139417640
Length
528 bp
Sequences
Splice sites
5' ss Seq
CAGGTGAGG
5' ss Score
10.07
3' ss Seq
TCTTGTCCCCTTGTCTCCAGGGA
3' ss Score
9.72
Exon sequences
Seq C1 exon
CTGTGGCGGGGCCTTCGTGGGCCCGCGATGCCAGGACCCCAACCCGTGCCTCAGCACCCCCTGCAAGAACGCCGGGACATGCCACGTGGTGGACCGCAGAGGCGTGGCAGACTATGCCTGCAGCTGTGCCCTGGGCTTCTCTGGGCCCCTCTGCCTGACACCCCTGGACAATGCCTGCCTCACCAACCCCTGCCGCAACGGGGGCACCTGCGACCTGCTCACGCTGACGGAGTACAAGTGCCGCTGCCCGCCCGGCTGGTCAG
Seq A exon
GTGAGGGAGGACCCACAGCCTGAGGGGTGGGCAGACCCAGGCCCGCCGCCAGCTGCCCAGGCAACTTGAGGTACTTGGCGGGATCCAGGCCCGGGTCTCTGACCCGGAAGTAATTGGGAGCCCCTGCCCCAGGGTCCCTGCCCCCCTCCCAGACCTGGAATCGCCTCGTTTTCAGCTGCTTGCTCTGGCCCAACTCTTGCTGTCCCCGCTTCTGCGAGACAAGGGGAGCCTCTGTGTCCAGGCCGCCCCTGCCCCCTTCCTCCTGCCGTGCACTGGCCCTCACCTGTTAGGGTGAAGGGTGTCTGGAGGTGTCAGCTCTGGGAAGAGACGGCCCAGGCTCAGGCCTCTTGGGAGCTGTGGTCCTTCATCTGCCAAAGGCGACCGGTCTCACGGCAGGTCCTGAGGATCAAATGTGATAGCACCTAAGGTGGAGCCCAGGCTGGCACCTCCAGGTGGCCTGAAGGGAGGGAAGGCCCGGCCTCGGGGAGCAGTGAGGCCAGCACGACCCTCTTGTCCCCTTGTCTCCAG
Seq C2 exon
GGAAATCGTGCCAGCAGGCTGACCCGTGCGCCTCCAACCCCTGCGCCAACGGTGGCCAGTGCCTGCCCTTCGAGGCCTCCTACATCTGCCACTGCCCACCCAGCTTCCATGGCCCCACCTGCCGGCAGGATGTCAACGAGTGTGGCCAGAAGCCCGGGCTTTGCCGCCACGGAGGCACCTGCCACAACGAGGTCGGCTCCTACCGCTGCGTCTGCCGCGCCACCCACACTGGCCCCAACTGCGAGCGGCCCTACGTGCCCTGCAGCCCCTCGCCCTGCCAGAACGGGGGCACCTGCCGCCCCACGGGCGACGTCACCCACGAGTGTGCCTGCCTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000148400-NOTCH1:NM_017617:3
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:
PF0000822=EGF=WD(100=39.3),PF0000822=EGF=PU(90.6=32.6)
A:
NA
C2:
PF0000822=EGF=PD(6.2=1.8),PF0000822=EGF=WD(100=27.2),PF0764510=EGF_CA=WD(100=36.8),PF0000822=EGF=PU(81.2=22.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAGACTATGCCTGCAGCTGTG
R:
TAGGAGCCGACCTCGTTGTG
Band lengths:
358-886
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