Special

HsaINT0049336 @ hg19

Intron Retention

Gene
ENSG00000105877 | DNAH11
Description
dynein, axonemal, heavy chain 11 [Source:HGNC Symbol;Acc:2942]
Coordinates
chr7:21784056-21784681:+
Coord C1 exon
chr7:21784056-21784217
Coord A exon
chr7:21784218-21784487
Coord C2 exon
chr7:21784488-21784681
Length
270 bp
Sequences
Splice sites
5' ss Seq
GAAGTAAGC
5' ss Score
6.95
3' ss Seq
TTCTCTTTCTCATCCTGCAGGGT
3' ss Score
11.97
Exon sequences
Seq C1 exon
GGGATTTTATTTGCTTCTCCTGAGTGTTTAAAAGGTCCACTTGATTTAATACATCTGTGGCTTCATGAATCTGCCCGTGTTTATGGAGACAAACTGATAGACAAAAAAGATTGTGATTTGTTTCAGAGAAGAATGCTGGAAACTGCTTATAAATATTTTGAA
Seq A exon
GTAAGCGTATGAATGTCAGAGGTCACTACTTACTCCAACACCAACTGGGTATTGGGACTAAAGTTAGATGAGGGTATGAGAGAAGTGCACAAGGGCTTACCTTTTTGCAATGGCTGTGAATCCAGAATACACTTGGTCTATGCTTGGGAACATTCCACCCACCTACCCATGTGTGGGTCTGCAAGCTTTTCCCTTGCTAGGCCATGCTGCCTGCAGCTGGACCTCTATGGATGGTTGACATGCCATATTTTTCTCTTTCTCATCCTGCAG
Seq C2 exon
GGTATAGATAGTCACATGCTGCTTCAACAGCCCCTCATTTATTGCCACTTTGCTGATAGAGGGAAGGACCCACATTACATGCCAGTGAAGGACTGGGAAGTGCTGAAGACGATTCTTACAGAAACGTTAGACAACTACAATGAACTAAATGCTGCCATGCACCTAGTTTTGTTTGAAGATGCCATGCAACATGT
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000105877-DNAH11:NM_003777:50
Average complexity
IR-S
Mappability confidence:
NA
Protein Impact

No protein impact description available

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.000
Domain overlap (PFAM):

C1:
PF127752=AAA_7=PD(8.1=40.7)
A:
NA
C2:
PF127802=AAA_8=PU(7.1=29.2)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
Rat
(rn6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGTGGCTTCATGAATCTGCCC
R:
ACATGTTGCATGGCATCTTCA
Band lengths:
301-571
Functional annotations
There are 0 annotated functions for this event


GENOMIC CONTEXT[edit]

INCLUSION PATTERN[edit]