HsaINT0050668 @ hg19
Intron Retention
Gene
ENSG00000079805 | DNM2
Description
dynamin 2 [Source:HGNC Symbol;Acc:2974]
Coordinates
chr19:10906048-10908194:+
Coord C1 exon
chr19:10906048-10906115
Coord A exon
chr19:10906116-10908055
Coord C2 exon
chr19:10908056-10908194
Length
1940 bp
Sequences
Splice sites
5' ss Seq
CAGGCAAGT
5' ss Score
3.1
3' ss Seq
CTGCCCTCCGCATGACCCAGGAC
3' ss Score
5.27
Exon sequences
Seq C1 exon
ATGGAGTTTGACGAGAAGGACTTACGACGGGAGATCAGCTATGCCATTAAGAACATCCATGGAGTCAG
Seq A exon
GCAAGTTCCACGAGGAGAGTCACCACTGTTCCTTCCTCTCCGTGGTGCGACCCCCCAGCTAATTGGGTCACCCACACCTCTGAGTCCCTAATCGTTAGGCCTTAAGAGGGCTCTTGGATGGTTTTCTGTAGCTGCGAGCCCCTCCCTGAGGGTCTCCAAGGGCACATGAGGGTGGATGTGTCTTAGTCCTGCGTCCATTGCAGGCTTCAGGGCTGTCTGCAGCTCCTGATCAAATAGGGCTTAGTTCCTGCCCAGTCGGTTGGTGTGAACCTCATGCTAAACTAAGAATGCTCACTGCAGATTTGCCTGGGGAGGGGCGGGGCGGCACTGAATCAGGGTTTTGGGAAGCCAGCATGAGTCCCCATCATGGCTTCCTCGTGAGCCTCTTGGGTCCCCTCCTTATTCTAACAAAGGTAGTTGCTCCAGGTGTCTGCCCTTCCATCGCCGTGGGGTCCTCGGGTCACCCTGAGGGTTTCCGGGCAGTGGACTCAGGCATCCGACCCCACACATGACACAACCTTCATTCCTTGTTGGGGACCCGGCCAGGGCCAATGAAATTGCTGACCATGCTTTGTTTCTCTCTGACTTATCTCCCCTGCCCCCGGGTCTGGACGGTTTCAGGACCGGGCTTTTCACCCCGGACTTGGCATTCGAGGCCATTGTGAAAAAGCAGGTCGTCAAGCTGAAAGAGCCCTGTCTGAAATGTGTCGACCTGGTTATCCAGGAGCTAATCAATACAGTTAGGCAGTGTACCAGTAAGGTATTGCTCCCTCGGCAGGGTGACTCCTGACCTTGTGGAAACGGGGGTACGGGGGTTTGGTATCAGGCTCCCAGCGCCTCATTGGCCCCCACTGGTGCCTTTTCTCCCCATATCGCTTTGTGTCCGTGAACTTGGCCTCTCCCCAGAGGCTGGGGCAGGAGCATGTAGGCCTGGGCCCAGGCACACAGGGGAGTGCCAGGCCTCCTGGACTGGCCAGACAGATGCACAGTTGTCCCTGGGACCCTGATACCAAGCCTAGCATGTGTCTGATGAAATTGGGGTTTCACTGGGCTGTTGCTTTGCTGCCTCCTGGGAAGCAGAGAGGGACCCCCCGCGTCAACTGCTGGAGGCTGAGCTCCTTGAAGCTCCCTGGCTGTCACCCCTTCTTGACCAATGCCCGGCATTCTCAGACTTCCCTGGAGCCACCGACTTCTCTGTCCCTCAGCTCCGGGAATGGCCTGAATGCCAGCGACATCATGAGAGCCAGCTGGGGTCCTAAGTGCCCCTGCCCACCCCCTGCACCCCACGCTGTCCCCCAGGGGCAGCCCATTTTTGGATCCACTTAGTCACAGTGCCTCTATGCGCTCTCGACGAGCCACTGCCTCCACTCAGCAGGACGCGCCGGGCTCCCCCAACCCGCGCCAACGCCGCGGGCCTGGTTCCCAGGGCAGCACGCTTTGGCCAAGCAGCTGAAATGCCTCCCAGTGGGCAGTCTGTGCTTGCGCGACCACAGTGTCCCCAGCGCTCCGGGTTGCCAGGGAATTTCTGCTTGAGCCCCTCTGTTCTTAGTCTGGAAAAGCCCACATTTGCTGCTTAAGCTTCTTCGATTAGAAAAGGGAGGGGGAAAACAGTCCAAACAGGTTGGAAAACGCTCGTCCTAGAGCCAGGTGTCATGGACATGAATGTTAGAGGACTCCGCACACCTTGGCTGTCTGTCTGTGCAATGACAACCCCCCGTGGCCCTTCTGTAACTACACCCCAGACCGAGCCCACACCCCCAAACCCCAGACCTCTTTGATCCGAAGCAGCTTCCGGGGCAAATGCGGGCGCAGGCTCCCCCATGCATGGACTAATCAGATGACTCTCGTTTCTTCTCTTCTCTCTGTCTCCTGTCCTGCGTGTGTGGCCTGCACTGTCCCTGGGTGTCTTTCTGCCTCATCCTGCCCTCCGCATGACCCAG
Seq C2 exon
GACGGGGCTCTTCACCCCCGACATGGCCTTTGAAGCCATTGTGAAAAAACAGATTGTAAAACTCAAAGAGCCGAGTTTGAAGTGTGTTGATCTCGTGGTCTCAGAGCTGGCCACGGTCATAAAAAAGTGTGCCGAGAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000079805-DNM2:NM_001005361:9
Average complexity
IR-C
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:
PF0103115=Dynamin_M=FE(7.5=100)
A:
NA
C2:
PF0103115=Dynamin_M=FE(15.6=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Conservation
Rat
(rn6)
No conservation detected
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGGAGTTTGACGAGAAGGACT
R:
TTTTATGACCGTGGCCAGCTC
Band lengths:
191-2131
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
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)