Special

BtaINT0050345 @ bosTau6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr19:54351840-54353398:+
Coord C1 exon
chr19:54351840-54351992
Coord A exon
chr19:54351993-54353272
Coord C2 exon
chr19:54353273-54353398
Length
1280 bp
Sequences
Splice sites
5' ss Seq
CAGGTGCGA
5' ss Score
7.75
3' ss Seq
CCCCGTGGCTCCGTCCCCAGGTA
3' ss Score
10.43
Exon sequences
Seq C1 exon
GTGAGCCGCCATCTGTCCAAGCTCTTCGACAGCCTGTGTAAACTGAAGTTCCGCCTGGACGCCAGTGGGAAGCCGCTCAAGTTCGGCCTGGGCATGTATAGCAAGGAGGACGAGTATGTGGACTTTGACCAGGAGTGCAACCTCTCGGGGCAG
Seq A exon
GTGCGAGCCGCCGCGGGACGCGCAGAGCACTGCCCTGGGGATGGTGGTGCCCCGTGACCGGGACCGCGTGGCCAGACAGGCTGTCAGCAGCAGCCCGTGGCCAGCCCTCTCTCCTCTTCTCTCAGCCTTGCAGAACAAATGCTTAAGGGACGTCTTTATAGGAGTCCCTGCACAGCCTTACCTATGCAGTCTGAGGTGACCCGTGAAAAGAAAGGAAGGAGAAAGGAGGGAGGGGGAAAGGGAGGGAGAGAACAGATTTATTAATGCCCTTAAATCCTCATCGTTTTATTATTATTAATGCCAAGGGGGCCACTTTGGAGGGTGCCTTGCACACCTGCCAAGGTCTCATCCCTGTTCAGCATGATGGGCTTTACAGCTTCCATATTTAGCAGAGGGCTCCTCTTACCCTGGGCAGCCCAGCCCCAGTCCCACCTCCCCAGCCCGGGAGGCTTCTCCCTTCTGCTGACAGCAAGCTTCCTGGCTGCCCTCTCCCCCATCTTTTTGCCCAAGTATTATTCAAGCATCCAAATCAATTCTTACATTTTGCCTAAGCAAAATGTAATTTGGAGGTAAATTGGCTTGGGGCATTAAAAATCTCACGCGAGAAAACTCGAGCTCCAACAAGTTGAATTCGGAGTGCCTGGCCGGACAGGGTGACGCAGGATCCATTCATCGGTTTGTTCAGACACTTCCCACACTTAACCACTTACAGACATAACCACTGAACTACAGCCTGCACTGTGCTTCTATCAATAGCTTAAAAGAAAAACCAACCTGATTATCCCATTCAGGTATTTTCCCCCTGGTGGCAGTTAGTTGAAGGTTTGTATTTCAAAATACACGCAAGGGTCATCAGCCAGTTTGTCCGCGTGACAAAGAATGCCCTTGAGGACAAGTGGGGCTCTGCTGGTCAGAATCCGCCTGGGACAGGGGGCAGCAGGGCCCGGGGGACAGATGCCCTGTCCCGGAACATCAGCACTACTTCGTGGGCTCAGACACAGACTGTCTTCTCTAGCTTTTTCTCTCGTTCCCTATCCCTTCTGTGTTTAGACACAGTGATTGCACACGAAAGCCCAATGCAACTAGTTTTGTGGGTACAGCGAGGCTTGCTGAACACATTTTTCCAGCAGGGCATTCTTACCGCTCAGAAAACCTGGGCATTTCTACCCCTGGAATGATGATACGGATGAGGACAAGTGGTAATTGATTTCGTAAATGTCAGAGCAAGTCATCGGATGAGACATGCTCACCCTCTCTGGTCCCCGTGGCTCCGTCCCCAG
Seq C2 exon
GTAGAGGTCTGGCTGAACCGGGTGCTGGACAGGATGTGTGCCACGCTCCGCCACGAGATCCCCGAAGCTGTGGTGACCTATGAGGAGAAGCCAAGGGAGCAGTGGATCTTTGACTACCCCGCCCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSBTAG00000000920:ENSBTAT00000022637:30
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:
PF083938=DHC_N2=FE(12.1=100)
A:
NA
C2:
PF083938=DHC_N2=PD(6.5=64.3)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Primers PCR
Suggestions for RT-PCR validation
F:
TGAGCCGCCATCTGTCCAAG
R:
CTGGGCGGGGTAGTCAAAGAT
Band lengths:
278-1558
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Pre-implantation embryo development