Special

GgaINT0038696 @ galGal4

Intron Retention

Gene
Description
neurogenic locus notch homolog protein 2 precursor [Source:RefSeq peptide;Acc:NP_001238962]
Coordinates
chr8:4197868-4198250:+
Coord C1 exon
chr8:4197868-4197987
Coord A exon
chr8:4197988-4198097
Coord C2 exon
chr8:4198098-4198250
Length
110 bp
Sequences
Splice sites
5' ss Seq
AAGGTAACG
5' ss Score
10.19
3' ss Seq
CTGCACTCTGTGTTTTTCAGGGG
3' ss Score
9.68
Exon sequences
Seq C1 exon
GTGTGAACTGCCAGGTAGTGGTTGCACCATGTTCCCCCGACCCTTGTGAGAACTCGGGAATTTGCCAAGAGTCTCCTGATTCCGAAGGCTACACCTGCCAGTGTGCCCCTGGCTGGGAAG
Seq A exon
GTAACGTGGCTGGGAACATCCAGGGCTTCCAGCACTCAGCAGTGTTGGCATCGAGCCTTTTGACCATCGACATAATGAGAGATCTTACTTCTGCACTCTGTGTTTTTCAG
Seq C2 exon
GGGAGAGGTGTACAGTGGATATTGATGAATGTCTCTCAAAGCCCTGCAAAAATCATGCTTTGTGCCATAATATTCAAGGCAGTTACCTGTGTGAATGTCGTCCAGGCTTCACTGGAGGAGACTGTGACAGTAACATTGATGACTGCCTGTCTA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000002922:ENSGALT00000039988:15
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:
PF0000822=EGF=PD(6.5=4.9),PF0000822=EGF=PU(90.9=73.2)
A:
NA
C2:
PF0000822=EGF=PD(6.1=3.8),PF0764510=EGF_CA=WD(100=75.0),PF0000822=EGF=PU(9.7=5.8)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
GTGTGAACTGCCAGGTAGTG
R:
AGTCTCCTCCAGTGAAGCCTG
Band lengths:
243-353
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]