Special

GgaINT0139598 @ galGal4

Intron Retention

Gene
Description
brevican [Source:HGNC Symbol;Acc:HGNC:23059]
Coordinates
chr25:499051-499703:+
Coord C1 exon
chr25:499051-499443
Coord A exon
chr25:499444-499528
Coord C2 exon
chr25:499529-499703
Length
85 bp
Sequences
Splice sites
5' ss Seq
AAGGTACAC
5' ss Score
7.56
3' ss Seq
CACCCTGTGTCTCCCTACAGGGG
3' ss Score
12.4
Exon sequences
Seq C1 exon
ATGACCTCAAGGCCCTGCAGGTGTCCATCCCGCGGCACCCAGCCCTGCACGCTGTGCTGGCAGGGGACGTCACCATCCCCTGCCTCATCACCTACCTCGCACCCCTGCCCACTGCCAGCACGGCGGGGCGCCGGGCTGTGCTGGGAGCCCCCCGGGTCAAGTGGACCTTCATCTCCGAAGGCAGGGAGGCAGAGATCTTGGTAGCACGGGGGGAAAGGGTGAAGGTGAGTGAGGACTACCGCCTCCGTGCCTCCTTGCCAGTCTTCCAGCAGCGCTACACTGACGCCTCTCTGCTGCTCACTGAGCTGCGCCCCAACGACTCGGGGATCTACCGCTGTGATGTGCAGCACGGCATCGAGGATGGCCACGACATCCTCGACCTCAGAGTCAAAG
Seq A exon
GTACACGCAGGAAGGGGAGCAGCACGATTTGGGGGACCCTGCCTGGATCGTCTCTCCTGGCTCCTCACCCTGTGTCTCCCTACAG
Seq C2 exon
GGGTGGTGTTTCACTACCGTGGGGGTTCCACACGCTACACCTACACTTTTGCTGAGGCTCAGGAGGCGTGCACTGCCATCAGTGCCAGCATTGCCACCCCTGAGCAGCTGTATGCTGCCTATCTGGGCGGCTATGAGCAGTGTGATGCTGGCTGGATCGCTGACCAGACTGTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000013237:ENSGALT00000021615:3
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:
PF0768612=V-set=PU(92.7=96.2),PF0019312=Xlink=PU(0.1=0.0)
A:
NA
C2:
PF0768612=V-set=PD(6.6=15.3),PF0019312=Xlink=PU(60.4=98.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
CTACACTGACGCCTCTCTGCT
R:
CCTGAGCCTCAGCAAAAGTGT
Band lengths:
182-267
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]