Special

HsaINT0049565 @ hg19

Intron Retention

Gene
ENSG00000187775 | DNAH17
Description
dynein, axonemal, heavy chain 17 [Source:HGNC Symbol;Acc:2946]
Coordinates
chr17:76455866-76456339:-
Coord C1 exon
chr17:76456244-76456339
Coord A exon
chr17:76456084-76456243
Coord C2 exon
chr17:76455866-76456083
Length
160 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAAG
5' ss Score
9.06
3' ss Seq
ATCCCGTCTGTCATTTGCAGAAC
3' ss Score
10.85
Exon sequences
Seq C1 exon
AACGTCACTGAGAAGCAAAAGGCCTGTGAAACAGACCTGGCCAAAGCAGAACCGGCCCTGCTGGCAGCCCAGGAGGCTCTGGACACTCTGAATAAG
Seq A exon
GTAAAGGGGGAGGGAAAGAAAGGGGACCCCTGGCCTGGTTGGAGAGGAAGCTGCCTTCGCTGTTGGCGTGGGTGGTGACACACTCATGGCGGCTTCTTCGGGGCATCACCGAGGACCCGGTCCAAACTCCCATCGGACCCATCCCGTCTGTCATTTGCAG
Seq C2 exon
AACAACCTGACAGAGCTGAAGTCCTTTGGGTCCCCGCCGGATGCTGTGGTCAACGTCACCGCCGCCGTCATGATTCTGACCGCACCTGGGGGCAAGATCCCCAAGGACAAGAGCTGGAAGGCGGCCAAGATCATGATGGGCAAGGTGGACACCTTCCTAGACTCCCTGAAGAAGTTCGACAAGGAGCACATCCCTGAGGCCTGCCTGAAGGCCTTCAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187775-DNAH17:NM_173628:59
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.062 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF127772=MT=FE(9.0=100)
A:
NA
C2:
PF127772=MT=FE(20.9=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
CAGACCTGGCCAAAGCAGAAC
R:
GGATGTGCTCCTTGTCGAACT
Band lengths:
258-418
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