Special

HsaINT0049425 @ hg19

Intron Retention

Gene
ENSG00000174844 | DNAH12
Description
dynein, axonemal, heavy chain 12 [Source:HGNC Symbol;Acc:2943]
Coordinates
chr3:57494109-57494939:-
Coord C1 exon
chr3:57494867-57494939
Coord A exon
chr3:57494268-57494866
Coord C2 exon
chr3:57494109-57494267
Length
599 bp
Sequences
Splice sites
5' ss Seq
TGTGTGAGT
5' ss Score
5.84
3' ss Seq
ATGGTGTTTTGCTTTTCCAGAGG
3' ss Score
8.83
Exon sequences
Seq C1 exon
TGCAGAGCGTTCTTGTGAAACCACCAGTTAAATCGCTTGAAGATGAAGGAGGTCCTTTACCTGAATCTCCTGT
Seq A exon
GTGAGTAAATTATTTTAAAAACAGTACTTCATCCAATTTTTGATATAGATAAAAAATAAACTGATCTTACCTTCAAGTATACAATTGTGATGCTCAAAGGTATTTTGAACACATCTAAAAAAAAAGTACTCTTGTTTTTACCTCAGAGGTATTCTCTCTACTATGCTCATTTAGTTCTGCATACATAACTGGGGAGATCTTTATGAATGCATAGCTTAACTTAGCCTTGAGTAAGCTTTGGGGTATGGCAGACAGATTTCTCCAGCGCTTTTCTTTAGTCCTAAAGACTGTGTTCTTTCATTTTTACCAGGATAACTGAGCCAAAGCACAGTGGAAGTTAGCAGAGCTCTCAGATCTGGCCCATCACTCTGCCTTACTCACAAATTATTTCTGTTCTCTCTGAAGATAATGCAGTTTTGAGTTCTTGATGTGTTTTTATTAAATGCATATATCTTAAGGTTCCCATTGCTGACCACAGCTCCCTCTTCTCAAGCCCCAGTTTTCTCACTTCAATACTAATTTCATGTTATAAGCATTATTTCCTAAAGTTTAGGGTGTATTATTTTCATCATGTTTGATATGGTGTTTTGCTTTTCCAG
Seq C2 exon
AGGCCTAGATTATTCTAATCCTTGGCATTCTAGCTATGTGCAGGCAAGAAATCAAATATTCTCTAATTTGCACATTATTCATCCAACTATGAAAATGTTACTGGACCTTGGTTATACAACATTTGCTGATACAGTTTTGTTGGACTTCACAGGAATTAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000174844-DNAH12:NM_178504:6
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

No protein impact description available

No structure available
Features
Disorder rate (Iupred):
  C1=0.480 A=NA C2=0.037
Domain overlap (PFAM):

C1:
NO
A:
NA
C2:
NO


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
Associated events
Conservation
Rat
(rn6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGCAGAGCGTTCTTGTGAAAC
R:
AATTCCTGTGAAGTCCAACAAAACTG
Band lengths:
230-829
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]