HsaINT0112275 @ hg19
Intron Retention
Gene
ENSG00000078114 | NEBL
Description
nebulette [Source:HGNC Symbol;Acc:16932]
Coordinates
chr10:21147169-21148755:-
Coord C1 exon
chr10:21148642-21148755
Coord A exon
chr10:21147274-21148641
Coord C2 exon
chr10:21147169-21147273
Length
1368 bp
Sequences
Splice sites
5' ss Seq
AATGTAAGT
5' ss Score
8.62
3' ss Seq
GTTCCATGTTATTTTCATAGGTG
3' ss Score
8.86
Exon sequences
Seq C1 exon
ATTAAATACAAAGAAAAATTTGATAATGAAATGAAGGATAAGAAACATCATTACAATCCTCTTGAAAGTGCTTCTTTTAGGCAGAATCAGCTTGCTGCTACACTGGCGAGCAAT
Seq A exon
GTAAGTTGTAATTCATAGAAAATTATTTTCAAAATCTTTTGATTCTTGTTTTTTTTAGAATCGACTGTGTTGTAATTACTGATACTTAGCTTCCAAGTAATTTGTAGTTGAACTGAAGCATATTTTTCTAAAGCTTTTTCTGAGAAAAATATATTATTGTAATTAATTTTTAATGGTTACTGATTACTAATTAGTTAATAAGTAGGAATAGTGTTGCAAATGAAGTTATTATATCTGTTCAAGAGTGGAAATAGATTATAGAATTTTGCAGAGAAGTGGTCTGTATTAACACAAATTAGTGGTTAGGACAGTAGTTACCTCATGTAATTATGGCTATGAAATTGAGTTTATTGTAAAGTACTGCCTGGTACATGGTAATTTATCATATAAAGAAATTTTTAGAAATTTTACTGTAATGCCTCACAATTTATTTTTTATCCCTTGTGAAAATGCTGTGAAGTACTTCCTTATGTGATTTGTTTTCATTCTGTGTTTTTAAAAATCATCAAAATTCATTTTACAAGAAATGATGTTTTAAATTCTTGTTAGAATTAGAGTATAAAAACAGCAACATCAAAAAATTGATTACTTTGCTATAGTTGAAAATATTTAGATTTCCTTCTCAAGTATAAAAATTATGTATTATTGATCTGTTGCTTTCTTAGAAATAGAGATGAAATATACTTAAAGGAACATGGAACATAGTGCTGAAAGCTAAAGGTTTGGAGTCAGATTGCTTGGATCTAAATCCTGTTTTATCAAGTATTACTATGTCTTTGTCTTTCTATGCCTCAGTTTTCTTATCTATAAAATGGGGCTACTTAAAGTACCTACTTAATAAAGAGGTTATTGTGGAGATTCAATACTTAATACATATAAAGGAATTTAGAAAAGTGGCACATAGTAAGTGTGTGATATGCTTGCTATCAATGGTTTATTATTACTGGTATTATATTTTCAAAAAGTTGCTTTAAAAAAGCCTGTGGTGATAGGATGGGAAACATCAAAATCCTCAGATCTCCACAAAGCATAGTTGAAATACTGTAGTAATTTCTAAAGAATAAAGTGGCTATTCTCTTTATTTTTTGAAAGCAGAGTTACTGTGAAAATTACTTTATTCTATTGACATTACCCTTCCTGAATATGTGAACAACAAAAGGAATTATCCAAGTATTCTCAAGCCCATATAGAAATAACTTTTTAAAATTCATTCAGTAGTAAATCAGCACCATCTAGTGGCTCCTTGTAAATTCGTCTGTCCATTTACCACTAAATAGTCCTACTTTATGATGTATGAAAAATGCAATAATGCAAAAGCATAATATTTTCTTCTCCTCGATGGTATTTTGTTCCATGTTATTTTCATAG
Seq C2 exon
GTGAAGTACAAGAAAGACATTCAAAATATGCATGATCCAGTTTCAGATCTCCCAAATTTGTTGTTTTTAGACCATGTTTTGAAAGCCAGCAAAATGCTCAGCGGC
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000078114-NEBL:NM_006393:8
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact
ORF disruption upon sequence inclusion
No structure available
Features
Disorder rate (Iupred):
C1=0.500 A=NA C2=0.079
Domain overlap (PFAM):
C1:
PF0088013=Nebulin=PD(37.9=28.9)
A:
NA
C2:
PF0088013=Nebulin=PU(50.0=37.1)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Conservation
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Genotype-Tissue Expression Project (GTEx)
- 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)