Special

GgaINT0039346 @ galGal4

Intron Retention

Gene
Description
collagen, type XI, alpha 1 [Source:HGNC Symbol;Acc:HGNC:2186]
Coordinates
chr8:10268308-10268943:+
Coord C1 exon
chr8:10268308-10268361
Coord A exon
chr8:10268362-10268835
Coord C2 exon
chr8:10268836-10268943
Length
474 bp
Sequences
Splice sites
5' ss Seq
TCTGTGAGT
5' ss Score
7
3' ss Seq
TGTTCATGTGTTTACTATAGGGT
3' ss Score
9.05
Exon sequences
Seq C1 exon
GGTGAACCTGGAGAAGCTGGTAATCCTGGACCTCCTGGAGAATCTGGAACATCT
Seq A exon
GTGAGTCATTTGGTTTTGTCTTACTAACTTGTGTCACAGTAAAAAAAGACATAAGGTAGTGCTTACTTTAAGAAACATTTAATGAGATTACTTGTGTTTTTGTGTTTAAATTTTCAGTGAAGAACTTTCTTACACTTTTGAAATTTGTTTTTTACAACTGTATAACTATAAGTATAGCCACATCTCATAGCAAGATGTGGCAAATCTGTGAAGACTTCCTAAAAGAGTACTTGCTTTGATATGCATATTTTTTTCTCTATAGAAGCAATTCATTGATGCAGAATAGGTTCAGACTCACATGTGGTTGCAGATGTTTGCACTCAGACCTGGGGCTGAGGGCCTAATTTCCCATTCACATACCAACATTAATGAGGAATATCATTGCCCAGATCTGAAAAACAGTTTTGCCACTGTAATTTTTCTTTATACATTCAATTTCCAGACAATATTTTATTGTTCATGTGTTTACTATAG
Seq C2 exon
GGTCCAAAAGGTGAAAGGGGAGAAAAAGGTGAGGCTGGTCCACCTGGAGCAGCTGGACCACCAGGTGCTAAAGGACCTCCAGGTGATGATGGGCCTAAGGGTAACCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000005180:ENSGALT00000008321:50
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

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

C1:
NO
A:
NA
C2:
NO


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:
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]