Special

HsaINT1025134 @ hg38

Intron Retention

Gene
ENSG00000204301 | NOTCH4
Description
notch 4 [Source:HGNC Symbol;Acc:HGNC:7884]
Coordinates
chr6:32196925-32197594:-
Coord C1 exon
chr6:32197299-32197594
Coord A exon
chr6:32197073-32197298
Coord C2 exon
chr6:32196925-32197072
Length
226 bp
Sequences
Splice sites
5' ss Seq
CAGGTTAGC
5' ss Score
4.9
3' ss Seq
CTGGCCCTCTGTCTCCCCAGCTT
3' ss Score
9.49
Exon sequences
Seq C1 exon
ATGGGGTGACACCCCTGATGTCAGCAGTTTGCTGTGGGGAAGTACAGTCCGGGACCTTCCAAGGGGCATGGTTGGGATGTCCTGAGCCCTGGGAACCTCTGCTGGATGGAGGGGCCTGTCCCCAGGCTCACACCGTGGGCACTGGGGAGACCCCCCTGCACCTGGCTGCCCGATTCTCCCGGCCAACCGCTGCCCGCCGCCTCCTTGAGGCTGGAGCCAACCCCAACCAGCCAGACCGGGCAGGGCGCACACCCCTTCATGCTGCTGTGGCTGCTGATGCTCGGGAGGTCTGCCAG
Seq A exon
GTTAGCACACACTGAGGTCCCTACAGGGAATGGGGCGAGCTTACAAGTAAAGCTGGACAGAAGCATCCCCTAGAGTTTGACAAGGAGGAAATTGGTGTGATTGGGAACCTGACAGGGAAACTGCGGAGGATGGCTGAATATGGATTGCGAGTGGGGTTAATAGTGTAAGGAACTCGAGTTGGCAGTCCAAGGTACCCCAGGGGTCACTGGCCCTCTGTCTCCCCAG
Seq C2 exon
CTTCTGCTCCGTAGCAGACAAACTGCAGTGGACGCTCGCACAGAGGACGGGACCACACCCTTGATGCTGGCTGCCAGGCTGGCGGTGGAAGACCTGGTTGAAGAACTGATTGCAGCCCAAGCAGACGTGGGGGCCAGAGATAAATGGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000204301:ENST00000375023:27
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.525 A=NA C2=0.140
Domain overlap (PFAM):

C1:
PF127962=Ank_2=PU(83.9=78.8)
A:
NA
C2:
PF127962=Ank_2=PD(14.0=26.0),PF127962=Ank_2=PU(58.7=88.0)


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:
CATGGTTGGGATGTCCTGAGC
R:
CAGCATCAAGGGTGTGGTCC
Band lengths:
299-525
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains