Special

RnoINT0049247 @ rn6

Intron Retention

Gene
Description
dynein, axonemal, heavy chain 9 [Source:RGD Symbol;Acc:621799]
Coordinates
chr10:52597157-52600509:-
Coord C1 exon
chr10:52600383-52600509
Coord A exon
chr10:52597310-52600382
Coord C2 exon
chr10:52597157-52597309
Length
3073 bp
Sequences
Splice sites
5' ss Seq
CAGGTAAGT
5' ss Score
10.86
3' ss Seq
GCCATGACTTCCTTTCTCAGGTT
3' ss Score
9.37
Exon sequences
Seq C1 exon
GTTGTGCCTGTGTGAGAAAGCCCTTGCAGAGTACCTAGACACCAAGAGACTCGCCTTCCCTCGCTTTTACTTCCTGTCCTCCTCTGACCTGCTAGACATCCTTTCCAATGGCACAGCCCCACAACAG
Seq A exon
GTAAGTTGGGTAGCAACTTCAAGATCATCCAAATGGCTGGGACACCCCAGCAGGGGGCTCCTCTTCCATGTTACTTTGGGCATCTCTGCTCCCTTCAGCTTTCCACACACACACACACACACACACACACACACACACACACACACCCCACTCCTCACAGGCCACCCACCTCCCTAGCAGCTGAAACAGACGTGGAGTTGCAAAGGAATATGAAATTAAGCCTCCATCAGGAATGCCTTTGATCTGGCTCCGAGGTGACATCTAGTCAATTGTGGTCAACAGTGACAGCTATATAAAGAAGAATGATCTTCTGTCACTGGCAGGATGGCATGCATGGAGCTGGAGGAGGATGTGAAATGAGATAAGTCAGTCACTGGAAGACAGATGCCACATGTGGAGGCTCAAGTTGATCTCAGAGAAGCAGGGGCAATGACAGTGGTTACCAGAGGAATGGGGGATGGCTAGTGAGTGAAAGGTACTGGGTGTGCCATGACTCAATAACTTTTAAAATTTGATAGCATAATAAGATAACTGTAGTATACCACAGTTTACATATTTCAAAAAAGCTAATAGAAGTTCAGTAATTCCAATATAAGAAAGAACCAGTGTTTGATATAACAGTCATACCAACCTCCCTGACCTGACCATATTTGTTATATAGATCTGTTGAAGTGTCATATCAGACCCCATAAGTCAGTACAATTATTGTGTACATATTTGTAAATTACAAATAAGAAGAATGATGCCTAGAGTTTCCAAAAGGCCTATAAGTTGAGTGATTTTATTGGTTAAGTCATAGGGTGGTTCAGTCAAAAAAAGCCTGTGAGGAATCCCAGGTTTGGGGCTCTCCCTTTAATTCTAGTCATTTGTTGGCAGATAGGCTATTATTGTTTTAAATGGTTTTGCCTGTAAAAGTGAGGTTTGCTGAATAACATGGTTTTCGAGTGTCCGAATAACTAGATGAAGCTCCCTTGGTGTTTGTATCAACAGACAGTGGACCTCCAACTTGAATAAGACCCTGTGGAGGGTCTGTTATGAGCACACCCTCTCAGCCTCTCCCAGAACTTCTGATTTCCTGGATACAGGTGTGGCTGTAGGCTTTGTTTTTTTAGGTTTTCCCACATGAGCCCATACCTTTAGAGCCAATGCCATTGGCCTTGCAGGCTGTGTCTCCTGCTAAATGACAGGTGCTGCCTCTGTTCACACCTGAGATGAGTTCATAGATCTTTCATTTTGCCTCAGACTGAAGATGTATAGACCAAACATTCAACTGAGAAGTTGTTTGGCTGAATTCCTTCCCTCCCTTCTGGGTGATTTTTTTATTCATTTGAAGTACAAAGGGGTTTCTCTCTCCTTTTTTTTCTCACACAGAAGGTAGCATACTGCATATTCCTGTTTGTACTTTGTCTTCATGGGGGAAGGGCAGAGTGTCACTCTGTGGTCCAAGGCAACCATAAACTTGTGATGCTTGTGCCCCTGCCTACTGAGAATTCAGGCATGTGGTATTAGTTTTGTACTTTGTACTTTGTATTTTGTAATTTTTTACTTAGTTATATGTCTTTCATCTCTGTCTCTGTCTCTCTGTCTCTCTCTGTCTCTCTGTCTCTCTCTCTTTCCCCACCCCAGCCCTCCATTCCAACATTTGCATGATACTCTATTCTGGTGTATCATAGTCACACCACTACATCACTATTATTTTCCTATCTCAAATGAAGTGGCATTGGTGCCACCTTGTGTTTTGGAGACCCATCTTTTAGACCTAGAGATATTCCTAGAGAGTGCTGGCTGAAAGTAAATACACAACATCCTTGTTTGCACACACAACAATGCTTCCCTACATGGGAACTGTCCCCTTGGCATCACTGCCAACCATGCCTGAGAACTTCTCCAACAGAGCCAAAAATCAGATCCAGCAGGTCTTCGGTTTACTTGTTAATAAGAAGCAAATACTAAAGGGCATCGTCCTTGCATTTGTGGTCCTTCTGATTTTAGCCTGCAGATTGAGTTTCCCCAGTGGCCCAGGCACAGTGAAGTTGAACTATATGTCATATCAGTATTCTGCTTAGAGTTGTACTAACCCCATGTGTAGAAAGGGTCAGACTGTCCTCATCCTGTCTATAGCTTTAGTACCTAAGGTACTCATTCATAAGTATTCACTTCTCATTTAGTTGTAATAAATAATCCATTCCTCCCATATCCTAGTGAATGAAGCACAGTAAAGGTATTTCCTGACCCCTCTTCTGTGTGAGCAACTTAATGAATTGACTTAGAAGTCATAGTGACAGTAATTTCTTTTTTATCTAGATGTCTATAGAAATCAAAATGTATATTAATATGCAAAATATGTTTTTATTTATGTGTTTGCTTTATTTTGTTAGTTTACTGACACTTGAGATTTACCACTACCTGGAAACCATGGATTCTGTTGTCTTGACAGTTTTCTTCCACAATGTTTTAGAACATTTCTATTATACTAATCTGCCCCTGTCCCTTTAGGTTTTCCACACATCTGTAAACTGAGGTCTGTTACCTTTGACTGCAGAAACCGTCTTCTCTTTGAGTGTAGACTTAGCTCTTGGTCCACTTCCTTGGCATTCTTCAGAACTTCTTCATTTAGTTTTTGTGTCAGTTGAACCTCGAGTGCTGTTAATGCTGCTGTAAATTGATTTTGAATTTGCTTCCTTCGTTTCTTACCAGCCCATCTTTCATCTTGCGATTTACAGTGCCTACATTTCTTTTATTTAAATGAGAGCAAAACCAAATGATAGTTATTTCCCTTTAGGTTACACATTCATTCCTGTTTGCACTCCTCTGATCTCAGGAGAGGGCACTGACTCCCATGATGGAATCACAATGGTGCAATGTTCCCACCAGTTTTATATTCTTTTGGTCATGTCTGTCCAGCTCACATGGTCCCTATCTTCATACCTGCATAATTGCTGTAATCTTCCTTCAACACTCTTGACATTCACCCTTCTATGTTATGCTAGAGTTGTCCCTGGCATACCCTAGACAACCATGATCAGCTTCCTGTGCATCCTCTCAAACCCTTTGCCATGACTTCCTTTCTCAG
Seq C2 exon
GTTCAACGTCACCTTTCCAAGCTCTTTGACAACATGGCTAAGATGCAGTTCCAGTTAGATGCCAGTCAGAACCCAACCAAGACAAGCCTGGGCATGTACAGCAAAGAGGAGGAATATGTGGCCTTCAGTGAGCCCTGTGACTGCAGTGGACAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSRNOG00000004171:ENSRNOT00000005583:22
Average complexity
IR
Mappability confidence:
NA
Protein Impact

ORF disruption upon sequence inclusion

No structure available
Features
Disorder rate (Iupred):
  C1=0.000 A=NA C2=0.020
Domain overlap (PFAM):

C1:
PF083938=DHC_N2=FE(10.1=100)
A:
NA
C2:
PF083938=DHC_N2=FE(12.1=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA


Other Skipping Isoforms:
NA
Associated events
Conservation
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]