Special

HsaINT0112142 @ hg19

Intron Retention

Gene
Description
nebulin [Source:HGNC Symbol;Acc:7720]
Coordinates
chr2:152354140-152354866:-
Coord C1 exon
chr2:152354774-152354866
Coord A exon
chr2:152354233-152354773
Coord C2 exon
chr2:152354140-152354232
Length
541 bp
Sequences
Splice sites
5' ss Seq
TCGGTATTT
5' ss Score
4.52
3' ss Seq
GATGCTTTCTTATCGCACAGGTG
3' ss Score
8.99
Exon sequences
Seq C1 exon
GTGCTATACAAAGAAAACCTGGGGACAGGAATTCCAATCCCCATCACTCCTGAGATGCAGAGAGTCAAACACAATCAAGAAAACCTTAGCTCG
Seq A exon
GTATTTTGGAAAGAAAGGGGAAAAAATGCCACTTAACTTCAGAATTAAACTGATCTTTACATTTATTTATTTTTGTTTGAAGCCCATTTCCCTTCTTTGCTTCTAATACATCTTATATTACAAAAGGATATACTTTCCCATTTCTATAATACAGTTAATGTCAATTTTTTACTTCATCTGATATTTACAAACAAACATGTTTTAAAAATAATGAATGTTTCCATTTGTGTGGATAACAACACCGAGTTCTAACAGTCTCAAATCCTCATGTGATTGTTTAGGAGGCACCGTACTCACAAAAATGAAAAAAAATAACATGGATAACTCTGACAGCCCTTCCTCAGCAGCTGAAGTCCCTGCTTCTCTAGAGGGTGCAGATTCCCTATCCCAACAACAGCTTCCACTAAAGTAGTCGGTGGCATTTTGTCAGCATATAACTTCTGGCTCCTTGGATGACTGTGTTTTTTCCTCATCCTTAAAAAGTCCCAAGAAATGAAATGTTACTCATGGTTGTTTTTCTGGATGCTTTCTTATCGCACAG
Seq C2 exon
GTGTTATACAAAGAAAACATGGGCAAGGGAACCCCTTTACCTGTCACTCCCGAGATGGAAAGAGTCAAACACAATCAAGAAAATATTAGCTCG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000183091-NEB:NM_001164508:170
Average complexity
IR-C
Mappability confidence:
NA
Protein Impact

No protein impact description available

No structure available
Features
Disorder rate (Iupred):
  C1=0.627 A=NA C2=1.000
Domain overlap (PFAM):

C1:
PF0088013=Nebulin=PD(32.0=25.0),PF0088013=Nebulin=PU(57.1=50.0)
A:
NA
C2:
PF0088013=Nebulin=PD(39.3=34.4),PF0088013=Nebulin=PU(57.1=50.0)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Conservation
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
Chicken
(galGal3)
Zebrafish
(danRer10)
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]