Special

GgaINT0081295 @ galGal4

Intron Retention

Gene
Description
SR-related CTD-associated factor 8 [Source:HGNC Symbol;Acc:HGNC:20959]
Coordinates
chr3:49626632-49628669:+
Coord C1 exon
chr3:49626632-49626732
Coord A exon
chr3:49626733-49628555
Coord C2 exon
chr3:49628556-49628669
Length
1823 bp
Sequences
Splice sites
5' ss Seq
AATGTAAGT
5' ss Score
8.62
3' ss Seq
CTGATTTTTGTTTTCAATAGATG
3' ss Score
9.39
Exon sequences
Seq C1 exon
TTTGCAGCACTACTCTTTGGGTAGGCCAAGTAGACAAGAAGGCTACACAGCAAGATTTGACCAACTTATTTGAAGAATTTGGACAAATAGAATCTATTAAT
Seq A exon
GTAAGTGAGCATGTTGTCATCCATTTTCAAGGATTTTAAGCAACTTAAACATACTTATGCCTCTGGATTCCTTTTTAGCCTAAGCTTGTGTTTAGGTGATTGTTACATTTTTTTTTAATCACTGTTTAAAAACTGTAGCTATGATATTTCCTTGTTAGTTTTTGTGTACTTTTGTTTGAGGCACTGAAGATAGCATGCTTCATGGTAAAATGACTTTGCCCTGACAAAAGGTAGGGTTGCACAGTTTTAAAAGTTTAAAAAACTTTTTTTGAAGCTGGCTCTTAACAAGTACAAGGTTGTGCCTTTTCACTTTATGTGTTGAGACACAGGAGTAGAGATTGTTTTTCCTTTCACTGATTGACAGAGTGTGATGTGATGTCCACGTTGGCTTGGTTATGTATGTGTGTAGCGGTGCTAAATGGCAGTCAGTGTATCTGAAATATTTATGAAAAGATACATAGTACTGTAAACGAGTGTATTTATAAAATGTGACCATAAAAGCATGCTTTCATTAGGAGCTGTATTTCTCATGATTTAGAATAATTTAGATTTAGTCTAGTAGAATCATAGAATGGCTTAAGTTGAAAGGGACCTTAAAGATCATCTAGTTCCAACTTCCTGCTGTGGATAGGGTTGCCAACCACTAGATCAGGCTACCTAGAATCCCATCCAACCTGTCCTCAAATACCTCTGAGGAGGAGGCTTATACGATTTCTTTGAGCAATGTGTTCCAGTGCCTCACCAACCACTGAGTAAAGAATTTTTTTGTAACATCTAGCCTAAATTTTCCCTCTATTAGTTTAAAGCCATTCTCCCTTGTCCTATCACTATTAGATGATGTAGAAAGCCAGTCCCCCTCCTGCTTTTAAGTACTGGAAAGCTGCAGTGAGGTCACTCCAGAGTCTTCTCTTCTCCAAGCTAAACGAGCCCAGCATTTTCAACGTTTCTTCGTAAGAGAGGTGCTTCTCTCTTTGATCCTTTGATCACCTTTGTGGCCCTTTCCTGGACCTGCTTCATCACCTCTGCATCTTTCTAGTGCTGGGGACCTCTCCAGATGGGGCCTCACAAAGTCAGAGTAGAGAGGGACAGTCACCTCCTTGGCTCTGCTGGCTATCCCTCTTTTGATGCAGTCCAGAATACTGTTGGCCTTCCAGGCTTCAAGGGCACGCTGCTGGCTGATGTCCAGTTTTTTATCCACCAGGATTGCCAAGTCCTTCTCTGAAGGGCTGCTCTCAGTGAGTTCCTCTCCCAGTCTGTATGCATACCTGGGATTGCCCAAGCCAATGTATACCTTGCATTTGGCCTTGTTGAACCTCATTAGGTTCATGTGGATCCACTCTGGATGGCATCCCTCTCTTCTATTGCATCAACTGTACCACTCAGCTTGGTGCCATCAGCAAACTTGCTGACTGTGCACTCGATCCCACTGTGTCACTGGCCACAAGTGAAGACTGAGGCAAAGAACTTGTTGAGTACCTCACAGTTTTTGGAGTTTAATGAGAGATAGTGACCTCTGCTTTTCTGAATTTGCCATAGCATCTCTCACTTGCCTGCTGCTTGTCATTTAAATCTGTCATGCTGCTTTTAGCACCCGTTCTTCAGCTTGCTGCTGCTTCTTGGAGACGTTGTAACTGTTGTACTCTACCAACTTCCCTCTTAGATCTTGCTGATGCTCAGAATTATTAATTATGCTTATTACAGTGATTGTTATCTACAGTATAAGCCCCTCCTTTTTTTTTCTATTGTAGTGTTTAGTGTAGATACGTAATCTGAAAGTACTATTTTTCCTGCTTTTTAAGACCACTGATTTTTGTTTTCAATAG
Seq C2 exon
ATGATTCCCCCAAGAGGTTGTGCGTATGTCTGCATGGTTCATAGACAAGATGCATATCGTGCTCTTCAGAAGCTTAGTTCTGGGTCCTACAAAATCGGATCTAAAATTATTAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSGALG00000013635:ENSGALT00000022182:13
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:
PF0007617=RRM_1=PU(41.8=82.4)
A:
NA
C2:
PF0007617=RRM_1=FE(55.2=100)


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:
TTTGCAGCACTACTCTTTGGGT
R:
TTTAGATCCGATTTTGTAGGACCCA
Band lengths:
206-2029
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]