Special

HsaINT0112199 @ hg38

Intron Retention

Gene
Description
nebulin [Source:HGNC Symbol;Acc:HGNC:7720]
Coordinates
chr2:151642574-151642869:-
Coord C1 exon
chr2:151642765-151642869
Coord A exon
chr2:151642682-151642764
Coord C2 exon
chr2:151642574-151642681
Length
83 bp
Sequences
Splice sites
5' ss Seq
GAGGTAAGT
5' ss Score
11.08
3' ss Seq
ACTATTAATGTCTATTTTAGAAA
3' ss Score
8.25
Exon sequences
Seq C1 exon
CGCCTCTATACAGAAGCTTGGGATAAAGATAAAACCACTGTCCACATTATGCCAGATACCCCTGAAGTTTTATTAGCTAAACAAAACAAAGTAAATTACAGTGAG
Seq A exon
GTAAGTAATATATTCATAGTGCGTGATACATTTTCCTTACAATGCACTTTATAAATCCAACTTACTATTAATGTCTATTTTAG
Seq C2 exon
AAATTGTATAAGCTTGGCCTAGAAGAAGCCAAGAGGAAAGGTTATGACATGCGGGTAGATGCCATTCCTATCAAGGCAGCCAAGGCCTCCAGAGATATTGCAAGTGAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000183091:ENST00000409198:59
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:
PF0088013=Nebulin=PD(37.9=31.4),PF0088013=Nebulin=PU(55.2=45.7)
A:
NA
C2:
PF0088013=Nebulin=PD(37.9=30.6),PF0088013=Nebulin=PU(55.2=44.4)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CGCCTCTATACAGAAGCTTGGG
R:
TAGGAATGGCATCTACCCGCA
Band lengths:
175-258
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