HsaINT0112134 @ hg19
Intron Retention
Gene
ENSG00000183091 | NEB
Description
nebulin [Source:HGNC Symbol;Acc:7720]
Coordinates
chr2:152362680-152363527:-
Coord C1 exon
chr2:152363423-152363527
Coord A exon
chr2:152362773-152363422
Coord C2 exon
chr2:152362680-152362772
Length
650 bp
Sequences
Splice sites
5' ss Seq
TCGGTATAT
5' ss Score
4.42
3' ss Seq
TCCTGATTCTGAATGCCCAGGTT
3' ss Score
3.47
Exon sequences
Seq C1 exon
CTCCAATACCAGTGTGACCTTAAAAACAGTAAAGGAAAAATTACAGTTGTTCAAGACACGCCAGAAATACTGCGTGTAAAAGAAAATCAGAAGAATTTCAGCTCG
Seq A exon
GTATATTTACTATTTATTTTGCATTTAATGCTAACCTAGTCATTTCACTCTCCTCTTTAAAAATATACTAGCCTTATATTGATACACACAATTAACATCTAACCTCCTCAGTAATACTAGCAGTGATTTGCTAAAATCCCCAATACTTTGCTCCAAAATCATCTCCAGAGACCATTTGAAATAACTTTAAATCTGCTAACAACGTAACTTTTATTTTTAAATTTTTTAATCCCAGGGCAGTAACATGTGTTGTCTTGCTCCAAGAAGATGGATTTCTTTTTGACATTGTGATTTCTTTTGTTATCCCTCCCCCAAATAACTGACTGAGTTTGCATTTCTTTAATGGATTTTGTGTTACATATGGGGAGGGTTTTGTTGTTAATCAACATTTCCTGGCTCTTCTCATCCTGTGTTAGTATGGTATACCACAATCTTAGAAGAAATCTTAAGATCTGGAAAGATCCATGTTGTATAACTGGTCTGAGTCACTGATACTGACATGGAAATGTCAGGTGCGATGCTCTGGCACTTGCCTGGGAACATCGTCTAGTGTCTTGTTTTCACAAAAGCCATGTGTCCTAGTCTTTCTCCAGGAACTGCTGGGTTTTCTTTTCTTCTGTGTTAACACTGTCCTGATTCTGAATGCCCAG
Seq C2 exon
GTTTTATATAAAGAGGATGTCTCACCAGGAACGGCTATCGGAAAGACACCTGAGATGATGAGAGTGAAACAAACACAGGACCACATTAGCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000183091-NEB:NM_001164508:163
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.091 A=NA C2=0.656
Domain overlap (PFAM):
C1:
PF0088013=Nebulin=PD(37.9=31.4),PF0088013=Nebulin=PU(66.7=45.7)
A:
NA
C2:
PF0088013=Nebulin=PD(25.0=19.4),PF0088013=Nebulin=PU(61.5=51.6)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CTCCAATACCAGTGTGACCTT
R:
CGAGCTAATGTGGTCCTGTGT
Band lengths:
198-848
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)