HsaINT0015064 @ hg38
Intron Retention
Gene
ENSG00000033627 | ATP6V0A1
Description
ATPase H+ transporting V0 subunit a1 [Source:HGNC Symbol;Acc:HGNC:865]
Coordinates
chr17:42513861-42514460:+
Coord C1 exon
chr17:42513861-42513978
Coord A exon
chr17:42513979-42514288
Coord C2 exon
chr17:42514289-42514460
Length
310 bp
Sequences
Splice sites
5' ss Seq
CGCGTGAGT
5' ss Score
8.4
3' ss Seq
TTGTGTCTCCCATTCCCCAGAGC
3' ss Score
9.35
Exon sequences
Seq C1 exon
TTTGACTTTGGGGACACCATGGTCCACCAGGCCATCCACACCATCGAGTACTGCCTGGGCTGCATCTCCAACACTGCCTCCTACTTGCGGCTCTGGGCCCTCAGCCTCGCTCATGCGC
Seq A exon
GTGAGTACCTCTCTCCGGGCTCCGGAACTCTAGTTTCCCCCTCTGTGGGCGCACTGTCAGTTGGGGGGCTTAAGTCAAATGGAAATTACATGAAGGTTCTGGAATTATTCAGGTTCCTGAACCCAAGGAGAATGAGTACAGACAGGAGGCTCAGCACTTGTGCCAGGTTAGCTCTGCATGGTGGTCCCACTAAGGCAGTGGGAAGCCAGGATCCAGGGAACCCTAGAGCAGGGGGATGGCAGAGCAAAATTCATGGCCTACAGCTGCCTCTTGCCAAACTGCACTGGATTTTGTGTCTCCCATTCCCCAG
Seq C2 exon
AGCTGTCTGAGGTGCTTTGGACCATGGTGATCCACATCGGCCTGAGCGTGAAGAGCTTGGCGGGAGGTTTGGTGCTGTTCTTCTTCTTCACTGCCTTTGCCACCCTGACCGTGGCCATCCTCCTGATCATGGAGGGCCTCTCGGCCTTTCTCCACGCACTGCGCTTACACTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033627:ENST00000393829:19
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:
PF0149614=V_ATPase_I=FE(21.8=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(12.0=100)
Main Inclusion Isoform:
NA
Other Inclusion Isoforms:
NA
Other Skipping Isoforms:
Associated events
Other assemblies
Conservation
Fruitfly
(dm6)
No conservation detected
Primers PCR
Suggestions for RT-PCR validation
F:
TGGGGACACCATGGTCCAC
R:
CAGTGCGTGGAGAAAGGCC
Band lengths:
271-581
Functional annotations
There are 0 annotated functions for this event
GENOMIC CONTEXT[edit]
INCLUSION PATTERN[edit]
SPECIAL DATASETS
- Autistic and control brains
- Pre-implantation embryo development