Special

HsaINT1011403 @ hg38

Intron Retention

Gene
ENSG00000187775 | DNAH17
Description
dynein axonemal heavy chain 17 [Source:HGNC Symbol;Acc:HGNC:2946]
Coordinates
chr17:78505293-78506846:-
Coord C1 exon
chr17:78506720-78506846
Coord A exon
chr17:78505446-78506719
Coord C2 exon
chr17:78505293-78505445
Length
1274 bp
Sequences
Splice sites
5' ss Seq
GAGGTAGGC
5' ss Score
8.99
3' ss Seq
CGCTTCTTGCCTCCTCCCAGGTG
3' ss Score
10.58
Exon sequences
Seq C1 exon
CTTGGCCATCTGTGAAAAGGCTTTGGCAGAGTATTTAGAGACGAAAAGACTGGCTTTCCCCCGGTTCTATTTTGTCTCCTCGGCTGACCTCCTGGACATTCTCTCCAATGGCAATGACCCCGTGGAG
Seq A exon
GTAGGCGGGGCCCCTTGCATTCCGGTGTTTAAGCCAACATCATGCCAGACCCCAGGTGGGCACCTCTACCTCAACCGCCCTAGGGTGGGGTAAGTGTCCTTGGACGTGCCCCATCATCTCCAGGAGGCCCTCTGCACCAGAAGCTGCCCTGGGGTCCCCAGCCATGGCAGAAACGTGGCAGGACTCGCCTCACATCCTGCTCTGCACTTGGCCTGGCTTTTGAGAAGTTAATTTGCCTCTCTGTGCCTCATTTTCCCCTTCTAGAAAATGGGTCGTATGCCAGAGGCTTAGTAAGACACTGTTTCTGAAAGACACACCTCTCAGTGGGTCTTGCTCTGGTCAGCTGGTTAAATCTCAGGGTCCCAAGAGCAAGGAACAGGTGCCTCCTTGGGGCTATTCTAAAAGAGAAAAGAGGTCAGGCACAGTGGCTCACACCTGTAATCCCAGCTACTCAGGAGGCTGTGGCATGATAATTGCTTGAACCCGAGAGGCAGAGGGTTGCCGTGAGCCAAGATCGCACCACTGCACTCCAGCCTGGGCGACAGAGTGAGACTCTGTCTCAAAAAAAAAAAAAAAAAATTAACTAGGTGAAGGGAAAGCGCTTGCATTTTATTTTGACCGTAAGGTTAGAGGTTACACAAGAAGAAGGGATATGCAAGAATAGACTGAGTGTGTGGCTTGGGATCTGGGACAGAACCTTCTCAAAAAGAAGAAATCTTATTTATTAATTTTTTTTATTTTGAGATGGAGTTTCGCTCTTGTTGCCCAGGCTGGAGTGCAATGGCGCGATCTCGGCTCACCACAACCTCTGCCTCCTGGGTTCAGGTGATTCTCCTGCCTCAGCCTCCCAAGTAGCTGGGATTACAGGCATGCACCACCACGTCTGGCTAAGTTTGTATTTTTAGTAGAGATGGGGTTTCTCCACATTGGTCAGGCTGGTCTCGAACTCCTGACCTCGGGTGATCCACCTGCCTCGGCCTCCCAAAGTGCTGGGATTACAGGTGTGAGCCACCATGCCCCACCAAAAAGAAATCTTCCAGAATGGATGTTTGGCTTAGAAGGGCTGCGGTTCCTGGCCTGGTTTCTGTGTCCTGACTCAGAGCAGTCTTCGCTGGTTCCTTTTGTTGACTTAGTCATGTTTAGTCAACGTTGATCAAAGATGGGGAGTATATTCCAAAAAGAACGATGCCTAAAACCACCCACGGAAAGCCCAAGCCACGCACATGCCTTTCAAATCCCCCGTTGCATAATTCCCGCTTCTTGCCTCCTCCCAG
Seq C2 exon
GTGAGCCGCCACCTGTCCAAACTCTTCGATAGCCTGTGTAAACTGAAGTTCCGGCTCGATGCCAGTGACAAACCTCTCAAGGTGGGCCTGGGAATGTACAGCAAGGAGGACGAGTACATGGTTTTTGATCAGGAATGCGACCTCTCGGGGCAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000187775:ENST00000585328:30
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(10.1=100)
A:
NA
C2:
PF083938=DHC_N2=FE(12.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
TGGCCATCTGTGAAAAGGCTT
R:
CGAGAGGTCGCATTCCTGATC
Band lengths:
272-1546
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]


SPECIAL DATASETS

  • Autistic and control brains