Special

GgaINT0124709 @ galGal4

Intron Retention

Gene
Description
leucine rich repeat and sterile alpha motif containing 1 [Source:HGNC Symbol;Acc:HGNC:25135]
Coordinates
chr17:1549021-1549696:-
Coord C1 exon
chr17:1549619-1549696
Coord A exon
chr17:1549090-1549618
Coord C2 exon
chr17:1549021-1549089
Length
529 bp
Sequences
Splice sites
5' ss Seq
AAGGTAACT
5' ss Score
9.01
3' ss Seq
GAAATTATCTGTTCTTCCAGGTT
3' ss Score
8.3
Exon sequences
Seq C1 exon
GTGCTGATTATTCATACAAATAATCTTACATCTTTAGTTCCAAAGTCCTGTAGCCTCCTGAGTCTCATAACTGTGAAG
Seq A exon
GTAACTGTGACTTTTATCAGTCATTCTAGCTGCATTAAAACACACTAGCCCCCAAAAATTCCTCCTGTCTGGCTGTTGTTACCAAAAAGTGGTAACAAAATGTGACGGCTCCATTTTGTAGATTTACAAAACCTGGTGGATCACTTGAATGTGGATGAGACTGGTGGTGGGGCCATCTGATTTTGGTCTTTCTGTGGAGCAGTTCAGCCCATGGACCTGCAGAAATATGTTTTTCTGCCAGCCTGATTTCATGGAGGTTATTTGTTCACTTGGCTCGTCCAGTTTTGTGGGACAGTTCCCGTGGTGCCACTCCTTTCCCTGGTCACCTGTTTGTTTATCAGTGTACAGAGTGCAGGGTTTTCAAAAGACCTGCAAGAGTGAAGTGCCTCTATCTCATGGAATACTTCAGACTCTTTTGAAGCCCTCTTGGGAAGAGATAATTTTCATTGCTCGATAATTCACAACCTTTCATTTTTGCATCATGACATCTTTCCCCAAGTCTGTTTGGTGAAATTATCTGTTCTTCCAG
Seq C2 exon
GTTCTAGATCTGCATGACAACCAGCTGGCATCGCTTCCTGCTGATATTGGTCAGCTGACATCTCTTCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000008819:ENSGALT00000014334:5
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:
PF127992=LRR_4=PU(6.8=11.5)
A:
NA
C2:
PF127992=LRR_4=FE(50.0=100)


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]