Special

HsaINT0049536 @ hg19

Intron Retention

Gene
ENSG00000187775 | DNAH17
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:2946]
Coordinates
chr17:76498673-76499093:-
Coord C1 exon
chr17:76498968-76499093
Coord A exon
chr17:76498781-76498967
Coord C2 exon
chr17:76498673-76498780
Length
187 bp
Sequences
Splice sites
5' ss Seq
CAGGTCTGA
5' ss Score
5.06
3' ss Seq
TGGGGGGTATGTACTTTCAGGTG
3' ss Score
6.44
Exon sequences
Seq C1 exon
GTGGAAGTGTGGCTGAATCGAGTGCTGGACCGAATGTGCTCTACCCTCCGGCACGAAATCCCAGAGGCCGTGGTGACCTACGAAGAGAAGCCGAGGGAGCAGTGGATCCTGGACTACCCAGCCCAG
Seq A exon
GTCTGAGGCGGGTGGGGGCTCGGCGGCGCCTCGTGGCTGAGATAAGGGGCGAGTTTCTTTGCGTTCATGGGCTCCGCTGTTAACTGTGGTCCCCTGGAAAACCATCTAAGCTTTCAGCAGGAATGTCTGCGTTAGCAGGCGCCAGCGATCGCTCACTGCGTGGGCAATGGGGGGTATGTACTTTCAG
Seq C2 exon
GTGGCCCTGACTTGCACCCAGATCTGGTGGACGACCGAGGTGGGCCTGGCATTTGCCAGGCTGGAGGAAGGCTATGAAAACGCTATCAGAGATTATAACAAAAAGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187775-DNAH17:NM_173628:32
Average complexity
IR-S
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=PD(6.5=64.3)
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Primers PCR
Suggestions for RT-PCR validation
F:
AAGTGTGGCTGAATCGAGTGC
R:
GCTTTTTGTTATAATCTCTGATAGCG
Band lengths:
228-415
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains
  • Pre-implantation embryo development