Special

HsaINT1025128 @ hg38

Intron Retention

Gene
ENSG00000204301 | NOTCH4
Description
notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]
Coordinates
chr6:32201117-32202599:-
Coord C1 exon
chr6:32202076-32202599
Coord A exon
chr6:32201501-32202075
Coord C2 exon
chr6:32201117-32201500
Length
575 bp
Sequences
Splice sites
5' ss Seq
CACGTGAGC
5' ss Score
5.62
3' ss Seq
CCCCTCTCCTTACCCCACAGTCC
3' ss Score
10.75
Exon sequences
Seq C1 exon
GGTTTTGAAGGCCCCACCTGCAGCCACAGGGCCCCTTCCTGCGGCTTCCATCACTGCCACCACGGAGGCCTGTGTCTGCCCTCCCCTAAGCCAGGCTTCCCACCACGCTGTGCCTGCCTCAGTGGCTATGGGGGTCCTGACTGCCTGACCCCACCAGCTCCTAAAGGCTGTGGCCCTCCCTCCCCATGCCTATACAATGGCAGCTGCTCAGAGACCACGGGCTTGGGGGGCCCAGGCTTTCGATGCTCCTGCCCTCACAGCTCTCCAGGGCCCCGGTGTCAGAAACCCGGAGCCAAGGGGTGTGAGGGCAGAAGTGGAGATGGGGCCTGCGATGCTGGCTGCAGTGGCCCGGGAGGAAACTGGGATGGAGGGGACTGCTCTCTGGGAGTCCCAGACCCCTGGAAGGGCTGCCCCTCCCACTCTCGGTGCTGGCTTCTCTTCCGGGACGGGCAGTGCCACCCACAGTGTGACTCTGAAGAGTGTCTGTTTGATGGCTACGACTGTGAGACCCCTCCAGCCTGCAC
Seq A exon
GTGAGCCTGAAATCCACTGGAGCCAGGGAAGGAGAGGGGTGGGTGAGAGGAGGAGGAAGGACGTAGATGGCTCTGAGTTACAGTGTGGCCACAGCCTTGGGCTCCAGGGAGTTTCCACCCTAATAACCATCACTAAACAGGGGTCGAAGACTCTGGACTCCAACCTAGGGTAATGGGGTGGCATCAGTATTTAATGTGGGGCGTGGCCTTTGGGCTCCTCTCTAAGAGTTGAAGGAACTCAGGTCTCAAGCCTCCTTCCCTAAGCCTTGCTGCCATGGAGTATTTCCCCTAGCAGTCAGCACCTCACAGAGGGAAAAGGGCCTGGGACTCTCCTTTAGAAACAGAGGAGAGCTTGGGAGGGTACAGAGAGGGGACAGTCTAGGGAGACAGGGGTGTTAGCAGACATTGGGGTGTCTGGACTACCATCCAGGACTTGACTAAGCTCATTGCTCCACAGCTGCCCCCACTTAGCAACCAAAGCCCTAGAGGGCACAAAATATGGGGAATTCTTTCTAGGGTGAAGAAAAGAGTCAGGTTTTAGGGAGGTCCTGAGTCCCCCTCTCCTTACCCCACAG
Seq C2 exon
TCCAGCCTATGACCAGTACTGCCATGATCACTTCCACAACGGGCACTGTGAGAAAGGCTGCAACACTGCAGAGTGTGGCTGGGATGGAGGTGACTGCAGGCCTGAAGATGGGGACCCAGAGTGGGGGCCCTCCCTGGCCCTGCTGGTGGTACTGAGCCCCCCAGCCCTAGACCAGCAGCTGTTTGCCCTGGCCCGGGTGCTGTCCCTGACTCTGAGGGTAGGACTCTGGGTAAGGAAGGATCGTGATGGCAGGGACATGGTGTACCCCTATCCTGGGGCCCGGGCTGAAGAAAAGCTAGGAGGAACTCGGGACCCCACCTATCAGGAGAGAGCAGCCCCTCAAACGCAGCCCCTGGGCAAGGAGACCGACTCCCTCAGTGCTGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204301:ENST00000375023:21
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=0.248
Domain overlap (PFAM):

C1:
PF0000822=EGF=PD(14.7=2.9),PF0006612=Notch=WD(100=22.9),PF0006612=Notch=WD(100=21.7),PF0006612=Notch=PU(12.8=2.9)
A:
NA
C2:
PF0006612=Notch=PD(84.6=25.6),PF068168=NOD=WD(100=39.5),PF076847=NODP=PU(4.6=2.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGTGAGGGCAGAAGTGGAGAT
R:
ACTCTGGGTCCCCATCTTCAG
Band lengths:
346-921
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains