Special

HsaINT0015058 @ hg19

Intron Retention

Gene
ENSG00000033627 | ATP6V0A1
Description
ATPase, H+ transporting, lysosomal V0 subunit a1 [Source:HGNC Symbol;Acc:865]
Coordinates
chr17:40647052-40647734:+
Coord C1 exon
chr17:40647052-40647206
Coord A exon
chr17:40647207-40647643
Coord C2 exon
chr17:40647644-40647734
Length
437 bp
Sequences
Splice sites
5' ss Seq
GACGTAAGT
5' ss Score
10.93
3' ss Seq
CTTTTTCCCTGTCATGGTAGTGA
3' ss Score
5.62
Exon sequences
Seq C1 exon
ATGTTTAGCACTGTGTTCAGTGGTCGATACATTATTTTATTGATGGGTGTGTTCTCCATGTACACTGGCCTCATCTACAATGATTGCTTTTCCAAGTCTCTTAATATCTTTGGGTCATCCTGGAGTGTACGGCCGATGTTTACTTATAATTGGAC
Seq A exon
GTAAGTTGCAGAAGAAGCTAAAATTCAAAGCTTATTCCTTTCATGTGCAGCCCTGATTTTTAAGACAAGTGGTAAACTGACACTTCTTTAGGAAGTGGTGACAGTGTCTCCTCATTCATGCTCCACACTGTGAGTTGCTTTGTGATTTGTTCAGCAAGTATCCAGGAACTAAGATTAGAAATGATTTTTTTTTTTTTTGGAAACTAAAACCAGATTCCCCAGTTCCCTACTTGATTGTGTGTTTGTGTGTTTAATTTTTCTTTTTGTCATTTTGGATCCCTCAGTCTCAGCTGCTAGTCTCTCCTCTTTATTTTTCCCCTCCCATTTTATTGAAGAGACAAGATAGCTACAGTAATTTATTTTGGGGTCAGTTTCTGGACCCTTGTTGTTTCCCTCTCTTGTTCAAAAATAATGTGACTTTTTCCCTGTCATGGTAG
Seq C2 exon
TGAAGAGACGCTTCGGGGGAACCCTGTTCTACAGCTGAACCCAGCCCTCCCTGGAGTGTTTGGTGGACCATACCCTTTTGGCATTGATCCA
VastDB Features
Vast-tools module Information
Secondary ID
ENSG00000033627-ATP6V0A1:NM_001130020:13
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(10.8=100)
A:
NA
C2:
PF0149614=V_ATPase_I=FE(3.7=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:
CTGTGTTCAGTGGTCGATACA
R:
AATGCCAAAAGGGTATGGTCCA
Band lengths:
230-667
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