HsaINT0049217 @ hg19
Intron Retention
Gene
ENSG00000197653 | DNAH10
Description
dynein, axonemal, heavy chain 10 [Source:HGNC Symbol;Acc:2941]
Coordinates
chr12:124281203-124283918:+
Coord C1 exon
chr12:124281203-124281379
Coord A exon
chr12:124281380-124283792
Coord C2 exon
chr12:124283793-124283918
Length
2413 bp
Sequences
Splice sites
5' ss Seq
GAGGTATGT
5' ss Score
9.81
3' ss Seq
TTGCTTGAATTCTTTGATAGGTC
3' ss Score
7.32
Exon sequences
Seq C1 exon
ATTGACATCATTAATAAAATCTTTGTCCAGAACCTTGAAAATCCACCACTGTATAAGAATCACCCTCCAGTAGCAGGTGCAATATACTGGGAACGATCTCTGTTCTTTCGGATTAAGCATACCATCCTCCGATTTCAAGAGGTACAAGAGATACTGGACAGTGATCGAGGACAGGAG
Seq A exon
GTATGTTGCTCTTGCTAGAATTGGCTCCTTTTGTATTTGATTTTTTTTTTTTTTTTGAGATGGAGTCTCGCTCTGTCGCCCAGGCTGGAGTGCAGTGGCGCAATCTCGGCTCACTGCAACCTCCGCCTCCCAGGTTCAAGCGATTCTCTTGCCTCAGCCTCCCAAGTAGCTGGGACTACAGGCATGTGCCACCACGTCCGGCTAATTTTTTTGTATTTTTAGTAGAGGTGGGATTTTACCGTGTTAGCCAGGATGGTCTGGATTTCCTGACCTCGTGATCTGCCCACCTGGGCCTCCCAAAGTGCTGGGATTACAGGCGTAAGCCATAGCACCCGGCCCTGTATTTAATGTTTTAATCCTAGACTGGCTGCCCTCCCCGATCCCATCCAGGAGAAGCATTAGATCAGGCTGCTGCCGCCATGCAGCACGCTATGTAGAGTGGCCCATTTGAGAAGCAGCTCAATTTCAGACCCATGCCTGTGAGTTAGAGGGTCTTTCTGTTGTCCTTGCATTCATGCTCATAGTAAACTGCCTTTTGCGTTCCTTCTTTTTCTTTTCTTTTTCTTTTTTTTTTTTTTAAGACAAGGTCTTGCTGTGTTGCCCAGGCTGGAGTGCAGTGGCACAATCACAGCTCACTGCAGCCTTGACCTTCTGGGTTTAAGCGATCCTCCTGCCTCAGCCTCCCGAGTAGCGGGGCCTACAGGTGTGGGCCACCACGCCTGGCCCATTTTTGTATTTTTTGTAGAGATGAGGTTGCACCATGTTGCCTGCCCAGGCTGGTCTCAAACTCCTGAGCTCAAGCAATCTGTCCACCTCGGCCTCCCAAAGTGTTGGGCTTACAGGCGTGAGCCACTGCACCTGGCCTGTGTTCTTTCTCTTTGGCATCTTAATACAGAAGACATCTTCCAGAATGTGGTCATGTGGGCTTCTTCCTGTATTGAATTTTCAGCTTCTTTGGAGGATGCCTACCATCTTTTCGATATGATCTCACCCCCCACCCATGGATTTTTATATGTTATATAGCAGAGGCTGGTAAGCCATTTCTTTGAAGATCCCGATAGTAAATATTTTAGGGGTTTGGACAATTTCTCTGCAACGACTCAACCTGTCGTTGCTGCAATAAAGTATCCCCCAGATAATACGTTTTGAACAGGCGTGGCTGTGTCCAATAAAACTTTATTTATGGATGCTGAATTTGAATTTCATATCTTTTTCTTGAGTTACAAAGCATTATTATTCTTTTGATTTCTTTTTAATCATCTAAATCATTTCCTTCTCTTCATGTAAAAGCTGTTCTTAGTTCATGGGTAGAGACCAAGGCAGTTCATGGACTGTGGTTTGCAGAAGGCTGCCAGTCAACCTAGATTTCAAGTTATCAACTATATTAGTCCATTTTGCTATAAAGAAACTGGGTAATTTATAAGAAAAGAGGTTTAATTGGCTCACAGTTCTGCAGGCTGTACAGGTAGCATAGCCTTCCTGGGAGGTCCCAGGAAACTCCCAATCATGGTGGAAGGCAAAGTGGGGGCAGGTACCTCACACAGTGGGAGCAGGAGCAAGAGAGAGTGAAGGGGCAGGTGCTGCCCACTTTCACTTGAGCAGATCTCCCAAGAACTCACTCAGCATCACCAGGACAGTCCCAAGAGAGGTGGTGCAAACCATTCACGAGAATTCCGCCTTCGTGATCCAGTTGCCTCCCAGCAGGCCCCACCTCCAACACTGGGGATTACAATGCAGTATGAGATTTGGGAGGACAGAGATCTGTGCTATATCACCATCGCAGACCAACTCTCCAAGCTTTGGGAAAATCTATTGACTTCCTTTTTCAAAATGTGTTTATATCTAATACTATTTTATATTATATTATTTAATATTATATAACTATATATTATTTATTATATTAACATTTTTATTTATTATATTTATAATGTATGTATACAAAATTATGTAGAAAGATATGAAAAAATGTTTATATATAATTATATAAAAATGACCAGGTGCAGTGGCTCACACCTGTAATCCCAGCACTTTGAAAGGCCGAGGTGGGCAGATCACCTGAGGTCAGGAGTTCAAGACCAGCCTGGCCAACATGGTGAAACCCTGTCTCTACTAAAATACAAAAATTAGCTGGGTGTGGTGGCATGTGCCTGTAATCCTAGCTACTTGGGAGGCTGAGGCAGGAGAATCGCTTGAGCCCGGGAGGCGAAGGATGTAGTGAGCTGAGATCGCGCTACTACACTCCAGCCTGGGCGACAGAGTGAGACTCCGTCTCCAAAAAAAAAAAAAAAAAATTATATAATGTTTATAATAATTTATATATTATATTTATAATTTGTATAAATTATCTGTGTAGAGCGAGATGAAAAATGTTATTTTCAAGGACAAAATGACGGTTGCTTGAATTCTTTGATAG
Seq C2 exon
GTCAAACAAAAATATTTGGAAGTAGGTAGGACAATGAAGGAGTATGAAGACAGAAAGTATGAGCAGTGGATGGAGGTGACGGAGCAGGTGCTGCCAGCTCTCATGAAGAAGAGCCTTTTGACCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000197653-DNAH10:NM_207437:12
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:
PF083857=DHC_N1=FE(26.2=100)
A:
NA
C2:
PF083857=DHC_N1=FE(18.6=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping 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)