HsaINT0049451 @ hg19
Intron Retention
Gene
ENSG00000185842 | DNAH14
Description
dynein, axonemal, heavy chain 14 [Source:HGNC Symbol;Acc:2945]
Coordinates
chr1:225305583-225306996:+
Coord C1 exon
chr1:225305583-225305701
Coord A exon
chr1:225305702-225306921
Coord C2 exon
chr1:225306922-225306996
Length
1220 bp
Sequences
Splice sites
5' ss Seq
AAAGTATGA
5' ss Score
3.87
3' ss Seq
ATTTTTGAAACTAATTTTAGGAA
3' ss Score
6.64
Exon sequences
Seq C1 exon
CCTCATCTTGTGAAATGCTTTGAAAATATAAAACAATTATTGATATGGAAACAAGACATTGGCCCTCCTGCTGTAAAAATGCTAATATCTGCTGAAGGGGAAGGTCTCGTGCTGCCAAA
Seq A exon
GTATGATAAATGTTACAAACTGTTTAGATTCTGTACAACGTCATTATTTAAAATCTCTGCTTTGAAATTTTTGATATATTATAAAAGTGCGCTAAGCAAACTGTTTCTTCAAAGATTATATCCTTACGTAAATATACTTTTGCCTTTCCATATTCCCTACAATACATAATCTCACCTTTGCTCTAATTAAAAGTTGAGAAAGCAGTCTTCAAACTCCTGGGTGCATTCTAATTTGCACTTACATTTTGTTCTGTCATTAAATTCTGCCTTAAGTTTCCTACTCTCTTTTTAGTGCTTTTTCCCTTTTTGGTTTTAGTATATGAATATAGATAAGAAGAAAATTGGCTATTTGGAGTTGTTGATGCTACTCCCACTACTGCTTCTGCTGATCTCTGGTTTCACTGTGGTTTGCTCCCAGGCAATAATGACAAACTAGGTCCTTCCATTACACTGGTTCAATTTGCCAGCCCCAGCAAGGGCTCTCTAACCTTTGGCAAGTGGTCCTGATGTAAGTTGATTTTTAAAAAAATGCTGTGCCCAACCCTTCTTATCTACCAAAATCCCTATTCCAACCCTGCTGTTTAAAAGATCCAGTGAGGAAGGCCGGGTGCAGTGGCTCAAGCCTGTAATCCCGACACTTTGGGAGGCCGAGGCAGGTGAATTACCCAAGGTCAGGAGTTTGAGACCAGCCTGACTAACATGGTGAAACCCTATCTCTACTAAAAATACAAAAATTAGCTGATCGTGGTGGCAGGCACCTGTAATCCCAGCTACTTGGGGGGCTGGGACAGGAGAATCACTTGAACCCAGGAGGTGGAGGTTGCAGTGACCCAAGGTGGCACCATTGCACTCCAGCCTGGGTGACAGAACGAGACTCTCTCTGTCTCAAAAAAAAAAAAAAAAAAGAAAAGAAAAATTCCAGTGAGGAATCCAAAACTGTTTTATAACACAATTTGTTTATCTTGTAAATACCATTTTACATGAAACTTATTTATTGTGTAAATTCATGATTTTGATATCAGAATTTCCTAAAGCATGTTCATATGTTTTCTGCATAGTTTTCAAAATTAAGATTTAGAAAAACCAAAAGGCAGTAGTAGTCCTTTGGCCCATGAATATTATTAAAGTATGTAGAAAATTTAGTCTACAGGCTTGTCAAAGGACTGAAACATGAATTAAAAAATAATTCTTCATGATATTATTTTTGAAACTAATTTTAG
Seq C2 exon
GAAAATTCGTGTAAGAAGTGCTGTAGAACAGTGGCTGGTAAATGTAGAAAAAAGCATGTTCGATGTGCTAAAAAA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000185842-DNAH14:NM_001373:25
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(55.6=46.9)
A:
NA
C2:
PF083938=DHC_N2=FE(55.6=100)
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Conservation
Rat
(rn6)
No conservation detected
Chicken
(galGal4)
No conservation detected
Chicken
(galGal3)
No conservation detected
Zebrafish
(danRer10)
No conservation detected
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
- Genotype-Tissue Expression Project (GTEx)
- 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)