Special

BtaINT0050191 @ bosTau6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:HGNC:2941]
Coordinates
chr17:54115289-54115938:-
Coord C1 exon
chr17:54115804-54115938
Coord A exon
chr17:54115506-54115803
Coord C2 exon
chr17:54115289-54115505
Length
298 bp
Sequences
Splice sites
5' ss Seq
ATGGTAAGA
5' ss Score
9.48
3' ss Seq
GGTATTTTCCTATGAACCAGGTA
3' ss Score
4.4
Exon sequences
Seq C1 exon
ATGGAGCAAGGTTATTTAGAGAGCCTGTTTGAGAAATACGTACCATACCTCATTGATGTGATAGTGGAAGGAATAGTGGATGGAAGACAAGGAGAAAAGCTGAAGACAATAGTTCCGCAGACAGACCTGAATATG
Seq A exon
GTAAGAAACTATCTTTGTTAGCAAAAATAAATTCTTCCTAAAGAGCTTTCAAAAGGGAAGCAAAGACATCAGATGGGTAAGATCTAACCTTGCCGGTTACTGACAAGGGAGACTCAATACTTCTTTTTGTGACCATGAGCAAGACAAGATACTGGGCTCCATCTGCCCAAACCAATATGGTGGGCCATATAATTCCCATCGTTCTGAGATCTGGGGTCCCAGGGTTTGTGACCAGAACTGACTCTTGTGGGGTTGTGTGGAATATATGGGCTGACCCAGGTATTTTCCTATGAACCAG
Seq C2 exon
GTAACCCAGTTAGCCAAGATGCTGGATTCGTTACTAGAGGGAGAAATCGAGGAGCCCGATCTTCTGGAGTGCTACTTCTTAGAGGCTCTGTACTGTTCTCTGGGCTCCTGCCTCCTTGAGGATGGAAGGGCTAAATTTGATGAATGTATTAAGCGCATTGCTTCTTTGCCTACTGCTGATACAGAAGGGATATGGGCCAGTCCTGGGGAACTGCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000016523:ENSBTAT00000029664:42
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=0.014
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:
TGGAGCAAGGTTATTTAGAGAGCC
R:
GTAGGCAAAGAAGCAATGCGC
Band lengths:
307-605
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development