Special

HsaINT0015061 @ hg19

Intron Retention

Gene
ENSG00000033627 | ATP6V0A1
Description
ATPase, H+ transporting, lysosomal V0 subunit a1 [Source:HGNC Symbol;Acc:865]
Coordinates
chr17:40652725-40653322:+
Coord C1 exon
chr17:40652725-40652941
Coord A exon
chr17:40652942-40653214
Coord C2 exon
chr17:40653215-40653322
Length
273 bp
Sequences
Splice sites
5' ss Seq
CAGGTACGT
5' ss Score
10.65
3' ss Seq
TCCTTCTTCTTACTCTGCAGAAA
3' ss Score
10.95
Exon sequences
Seq C1 exon
CTATTTCAAGAAGCCCCTGAATATCTACTTTGGATTTATTCCTGAAATAATCTTCATGACCTCTTTGTTTGGCTATTTGGTTATCCTTATTTTTTACAAGTGGACGGCCTATGATGCTCATACCTCTGAGAATGCACCAAGCCTTCTGATCCATTTCATAAACATGTTCCTCTTTTCCTACCCAGAGTCTGGTTATTCAATGTTGTATTCTGGACAG
Seq A exon
GTACGTCAGCCCAGAGGCAGACTGTCTGAGATGATTATACTTGATCAGGAAGCCAGATGTTTCTCTGACCCTAAAAAATTTATAACTGCCCTTCTATGGGACAATTCTAGGGCTTTGCCACAAAATGTGATAATTATTTTGAGAAATTGGATAGTGTTATTCATAGATTAGTAAGAAAGTACTGTTGGGGGAAATTTGTGCCATATTTGGAAACTGCGTATGTGATCGGTAGACTTTTATATGATGTACCTTGTCCTTCTTCTTACTCTGCAG
Seq C2 exon
AAAGGAATTCAGTGTTTCCTGGTAGTGGTTGCACTACTGTGTGTACCTTGGATGCTGCTGTTTAAACCATTGGTCCTTCGCCGTCAGTATTTGAGGAGAAAGCATTTG
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033627-ATP6V0A1:NM_001130020:16
Average complexity
IR-S
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(10.6=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(19.6=100)


Main Inclusion Isoform:
NA


Main Skipping Isoform:


Other Inclusion Isoforms:
NA
Associated events
Other assemblies
Conservation
Primers PCR
Suggestions for RT-PCR validation
F:
AGCCCCTGAATATCTACTTTGGA
R:
TACTGACGGCGAAGGACCAAT
Band lengths:
295-568
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