HsaINT0050090 @ hg19
Intron Retention
Gene
ENSG00000007174 | DNAH9
Description
dynein, axonemal, heavy chain 9 [Source:HGNC Symbol;Acc:2953]
Coordinates
chr17:11774915-11778501:+
Coord C1 exon
chr17:11774915-11775103
Coord A exon
chr17:11775104-11778265
Coord C2 exon
chr17:11778266-11778501
Length
3162 bp
Sequences
Splice sites
5' ss Seq
AAAGTACGT
5' ss Score
7.99
3' ss Seq
TGGTGTTTCTTCTTCACCAGACT
3' ss Score
7.07
Exon sequences
Seq C1 exon
GTTGGAGGACTCGCTTCTGAAAACGTGAGGTGGGCAGATGCCGTGCAGAACTTCAAACAGCAGGAAAGGACGTTATGTGGAGACATTTTACTTATAACGGCTTTCATTTCCTACCTTGGCTTCTTCACAAAGAAATACCGGCAGAGCCTCCTGGACAGAACTTGGAGGCCCTACCTGAGCCAGCTGAAA
Seq A exon
GTACGTATGGCCTGAATTTCTCCCGACCACATCAGCCTCTGGGCACCAATGGGAAGACATCACGGTCATAATTCGCATCCTCTGGTGTCCTCCTGCACACTCATCCCCACCACCCCCTGAGCACCAGGTGTGAAACCTGCGTACCCGTGTCCTTCCACACTGCCTTGCATTGCTGCCCACTGCCCTCCAGGCCACCTGGGGGCAGCACCTCTCCTCTGAATGTAGTCCTCCATGGGAACACTAGTCCTCTTCCCCGCGGGCTGTCTCCTAGCAATCCTTAAAGCTGTGAAACCTGAGAGATAGAAAAAGAACCATTTTCGTCTCTGATCTCCCCACTCCAGAGCCAGACTTCATAGGAGCAGTCAGGGGACGTTCCATTTCCCAGATCCTACATTGCACCTTGTTACTGGGCCCTAAAGCTACACAGCTTGTGCCAGTGACTCACAGATATCCTTCGTCGGCTTCCGTCCTGCATAATCCCATGAACAGCTGCTCACATGCTTCTTATTTGGGCAGTTCAGCTTGTCCTCCTCGTGTGGCTAGGTGGATGTTACTCCCAACCCATCCCTTTACATCACCCGCCCCCCACCCCCTGCAATGTAACTAAATGGAGAAATACTGGTTTCCCATTAAAGGGGATTCAAAGCTATACTTGGACGCGAGCATCAGAAGTTCTAATATTTTCTTGGCACTTTCGCATCACTTCTAGCAACCCACAAATACTTCCTGTGTATTTAGTGTGTCCTACCACTCCACTATACAGGAGGCACACAAAACGTTCAAGACCGGGATACCTTTGGCAAGTTCCCAGTCCACTTGAGGAGATTAGGCTCATAGAAGTCAGCGAAGGTGGGCCGGGCGCGGTGGCTCACGCCTGTAATCCCAGCACTTTGGGAGGTTGAGGCGGGCGGATCACGAGGTCAGGAGATCGAGACCATCTTGGCTAACACAGTGAAACCACGTCTCTACTAAAAATACAAAAAATTAGCCGGGCATGGTGGCGGGCGCCTGTAATCCCAGCTACTCGGGAGGCTGAGGCAGGAGAATGGCGTGAACCCGGGAGGCGAAGCTTGCAGTGAGCCAAGATAGCACCACTGCACTCCAGCCTGGGCGACAGAGCGAGACTCCGTCTCAAAAAACAAACAAACAAAAACAGTCAGTGAGGGTGAAAGTCAGCCCCAAATTTCACAACATAAGGTAAAAGCTGTATTCCAGATCTATTTGTAAGTAGAACCTTAGAACAAAAACTCTTTCTGTAGTGATGATTGTTTTCTCAGATCAGCTCATAAAACCCTGCTCACCTGACAATTAGCTGAACCGTAGTTTTTAAAATGCTAGCAAATAAACAAAAAATAAAGCAGCTGTTTGACTCATCCTAAACACTTTTGGAAAAAGGAAATTGTTGAAGGAACCATCATTAACTGAGTGAATGAAGAAGAAGAGCTCAGTAGCAGCTTAGTGAGGATTTTTCTGGCTTTGTTTGGATTCTTAAGCTTTTTTGTGTCATGGACGTCTTTGGCAGTCTGGTGAGACCTACGGATTCTTTCTCAGAATAATGATTTTGACACGTCAAATAGAATGCATGAGATTACAAAGGGAAAAAATATATTGGAACACAATTCTGGTCCCAGATAAGAATCCCCAAGGGGCTGATTTCCCTTCAGAGGTTTGCTGGATACTGTAGTACTGGCCATTTGTGCCCTTGTTAGATACAATTAAGAGGATGGGAGATGGTTTGGAGAGGTTTCCCTGGGATAATTGGGCAGAACAAACTTCAGAGAGGAGTGAGATGAAGGAGTTAAAAGGGTATTTGTCTAAACCTCGAAAGCATTATGCTAAGTGAAAGTAACCAGACACAAAAGGTCACATATTGTAGGATTCATTTATAGTAAAATATCCAGAATAAGAAAATCCAAGGGGACAGAAAACATATTCATAGTTTCCACGAGCTGGGGGTAGACAGAAATTGCGGGGGCTGTTGAATGAGTATGGGATTTGGGGGTGATGAAATGTTTTGGGGGTAGAGCCGATGGCTGCATAATGTTATGCATAGACTAAATGCCACTGAATTGTGCACTTTAAAATGATTAATTTATTTCATATCAATGTTACCTTAATTTAAAAAAATATATATGGGTCATCAATGAAAAAGATTGCCTGTAAAAAAAATTAAGTGAGCCCGGCGTGGTGGGTCACGCCTGTAATCCCAGTATTTTGGGAGGCCGAAGCAGGTGGATCGCCTGAGGTCAGGAGTTCGAGACCAGCCTGTCCAACATGGTGAAACCTCGTCTCTACTAAAAACACAAAAATTAGCTGGGTGTGGTGGCAGGCACCTGTAATCCCAGCCACCTGGGAGGCTGAGGCAGGAGAATCACTTGAACCCGGGAGGTGGAGTTTGCATGGAGCTGAGATGACGCCATTGCACTCCAGCCTGTGTGACAGAGCAAGATTCCATCTCAAAAAAAAAAAAAAAGAACTGAGTGAGCAGAGAAAGGCTAACAAAGAAGAAAAGGCAGTGTCTAGGGCACACACAGGAGCCCTGAAGGGGCCTAAGAGAGGCCACAGGCAAGTTCTCAGACTGATAAATACTCGGCAGCTTCCCCACAGGCACCAGCAGGCAGGTTTGCAAGAGTCCTGCAAGTGAATGGGGTGTTTGGGGAAGAGAAAAAGAAAACCCGTCCAGCCTCTTGCAAGCTGGTGAAACAGAGGAGAGGAAAGAGTGGTTTGTGCCGGTTGGTACAGACAGGAGCAAACCCACTAGGCATGGGACCTGGTGCTGGTTCATGGAGCGTGCACAAGAAACACAGACATATAGCAGAGAAATAACACTGTTAACATGGGTGAGAGTGTGTAGGAGGTCGTAGATTAAAATACAGATAATATAGTAGAAACTTGACTTAGGTAAAGATACCGAAAAACAAAGAATCAGTCACACGAGTTGAATTTCTGCAGTTATTCATCCATGGAGGGGAAAAAAAAAAGCTATCAGGACTTTAATAGAACCTGCTTCCAGAAATAATCACACAGCCAGAAAGGCATTCTTCAGTGGGATGTTGATCTTGCTTTTAAAGGAGTTGTGTCATTTGGTGAGTAACTGCATTCATCCCAGCTGAGAATGTCTGCTTCTGTTCTGAGCGTGGGGTGGTGTTTCTTCTTCACCAG
Seq C2 exon
ACTCCCATTCCAGTCACCCCAGCCCTGGATCCCCTGAGGATGCTGATGGATGATGCTGACGTGGCTGCCTGGCAGAACGAGGGCCTCCCAGCCGACCGCATGTCCGTGGAGAATGCCACCATTCTCATCAACTGTGAGCGCTGGCCACTCATGGTTGACCCTCAGCTACAAGGCATCAAATGGATCAAGAATAAATATGGTGAAGATCTCCGGGTCACGCAGATTGGTCAGAAAGG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000007174-DNAH9:NM_001372:52
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:
PF127772=MT=PD(16.9=92.1)
A:
NA
C2:
PF127772=MT=PD(2.9=6.3),PF0102514=GrpE=PD(18.6=20.3),PF097314=Mitofilin=PD(1.2=1.3),PF127812=AAA_9=PU(60.7=82.3)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
No suggested primer sequences
R:
No suggested primer sequences
Band lengths:
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
Other AS DBs:
FasterDB (Includes CLIP-seq data)
AS-ALPS (AS-induced ALteration of Protein Structure, links to PINs)
APPRIS (Selection of principal isoform)
DEU primates (Only for human)