Special

BtaINT0135300 @ bosTau6

Intron Retention

Gene
Description
solute carrier family 34 (type II sodium/phosphate cotransporter), member 2 [Source:HGNC Symbol;Acc:HGNC:11020]
Coordinates
chr6:46743390-46744017:+
Coord C1 exon
chr6:46743390-46743485
Coord A exon
chr6:46743486-46743896
Coord C2 exon
chr6:46743897-46744017
Length
411 bp
Sequences
Splice sites
5' ss Seq
GTGGTAAGT
5' ss Score
10.36
3' ss Seq
TTCTCATGTTTGCCACCCAGACT
3' ss Score
6.01
Exon sequences
Seq C1 exon
CTGGATAAAAGTATTCTCAACCAAATTGCAATGAATGATGAGTCGGTCCAAAACAAAAGTATGATCAAGATTTGGTGCAAAACTTTTACCAACGTG
Seq A exon
GTAAGTTTCTAAGAATATTGCTGGCTGGGTTAGCTCTTTTGTCTGTACTGGATAAAGCAAGATCTTGCCTTCAGACTGGGCATATAAAAGGTTGGGAGAAAGAAAAATCGAGGATTCCTGAAAAGTCAAAACTAACCAGTGAGAATCCTTAAGTCGTTGATTTCTAGATGGACAAACATGCTGTAGGACAGACAGGACCAGCCCACATCATGGACATGTTATTCCTGGCTAATTATGTTCATGTCTCCTGGCTTATCTCTGGCTGCCACCTTGCTTGCATTTATAGAGGGACTTGTGAAAGCAGTGCCCCACACCTATGGAGTCTCCCGTGATGCCCCGAATTTCCCTCCATTCCCCACCAGAAGTGAGGGTTGTAGACAATGCATAGTATTTCTCATGTTTGCCACCCAG
Seq C2 exon
ACTGAGAGAAATGTCACCGTCCCCTCGCCTGAGAACTGCACCTCCCCTTCTCTCTGTTGGACGGATGGTTTGTACACCTGGACCATCAAGAACGTGACCTACAAGGAGAACATTGCCAAGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000001545:ENSBTAT00000002023:9
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:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AAGTATTCTCAACCAAATTGCAATGA
R:
TGGCAATGTTCTCCTTGTAGGT
Band lengths:
206-617
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]