HsaINT0186001 @ hg38
Intron Retention
Gene
ENSG00000147130 | ZMYM3
Description
zinc finger MYM-type containing 3 [Source:HGNC Symbol;Acc:HGNC:13054]
Coordinates
chrX:71247734-71248312:-
Coord C1 exon
chrX:71248162-71248312
Coord A exon
chrX:71247907-71248161
Coord C2 exon
chrX:71247734-71247906
Length
255 bp
Sequences
Splice sites
5' ss Seq
AAGGTAAGG
5' ss Score
10.51
3' ss Seq
TCCTCTTCTCCTCTTTCCAGGCT
3' ss Score
11.47
Exon sequences
Seq C1 exon
GACCAAGTGTTCCAGTTCTGCTGCCGTGATTGCTGTGAGGACTTCAAGCGGCTTCGGGGTGTGGTGTCCCAGTGTGAGCACTGTCGGCAGGAGAAACTCTTGCATGAGAAACTCCGATTCAGCGGAGTGGAGAAAAGCTTCTGCAGCGAAG
Seq A exon
GTAAGGAGATGGGGAAGGGCAGAAGACACTATAACTCCCAGCCAGGGAGAATGGAGGAGAAGGGAGGGAGGCCGGGAAAGTGGTCCATGAGGCAGGGCCTTCTGCCCGGGATGTTCTACCCCCATCTCCCCTAAAGTTTTGGGCACAAGGGGCTGCTTAGAGAGAGGTTTCAGGTATAGCACCTTGAAAAGGTTGGGTCTCTTGCCCTTGGGTATCTGTGTCTCTGGACTCTCTTTCCTCTTCTCCTCTTTCCAG
Seq C2 exon
GCTGTGTGCTGCTGTACAAACAGGACTTCACTAAGAAGCTGGGCTTGTGCTGTATCACTTGTACTTACTGCTCCCAGACCTGCCAGCGCGGAGTCACCGAGCAACTGGATGGCAGCACCTGGGACTTCTGCAGTGAGGACTGTAAGAGCAAGTACCTGCTGTGGTACTGCAAG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000147130:ENST00000373998:11
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=0.000
Domain overlap (PFAM):
C1:
PF064679=zf-FCS=PD(34.1=27.5),PF064679=zf-FCS=PU(84.6=64.7)
A:
NA
C2:
PF064679=zf-FCS=PD(12.8=8.6),PF064679=zf-FCS=WD(100=69.0),PF064679=zf-FCS=PU(10.0=6.9)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
CCGTGATTGCTGTGAGGACTT
R:
ACCACAGCAGGTACTTGCTCT
Band lengths:
293-548
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains