H-InvDB x AHG DB
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H-InvDB_8.3 released on March 26, 2013.
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H-Invitational ID: HIT000101512 Accession number: D49400 Created date: 26-Mar-2013 Last modified: 20-Apr-2012
Definition: V-type proton ATPase subunit F; V-ATPase subunit F; V-ATPase 14 kDa subunit; Vacuolar proton pump subunit F;
 
 

Transcript original information
Accession number D49400.1
CAGE tag ID NA
EST ID NA
Clone Number NA
Experimental resources NBRC: NITE Biological Resource Center  NBRC ; HGPD: Human Gene and Protein Database HGPD ; Antibody: searching human antibodies at "BIO-kaimono.com" Antibody (ATP6V1F) ; Catalog: searching experimental product catalogs at "BIO-kaimono.com" Catalog (ATP6V1F);
Sequence data provider NA
Annotation project NA
Length of cDNA 680[bp] (No. of exon:2)[A:138 T:164 G:174 C:204]
Devision HUM
Molecular type mRNA
Library origin Cell type NA
Tissue type brain
Develpmental stage fetus
Mini-G
Sequence quality information
CDS feature Complete CDS
Kozak sequence NA
PolyA NA
Vector/adapter sequence NA
Frame shift NA
Remaining intron NA
Splice site acceptor (NAGNAG) NA
Transcript quality feature NA
Notes NA

Gene structure information  G-integra H-DBAS cDNA-genome alignment
H-Inv cluster ID HIX0033667
Genomic location  G-integra Help Chromosome 7
Location 7q32.1
Position 128502910- 128505902
Strand +
Possible duplicated location(s) NA
Gene structure 2 exon(s)
Database links RefSeq NM_004231NM_001198909
Ensembl ENST00000249289ENST00000492758
Entrez Gene Entrez Gene ID:9296
KEGG GENES KEGG GENES(9296)
GeneCard GeneCardATP6V1F*GeneCards is provided free to academic non-profit institutions.
Related H-InvDB links H-DBASH-DBAS;  G-integraG-integra cDNA-genome alignmentcDNA-genome alignment

Predicted CDS information
HIP ID HIP000027841
Predicted CDS 51..410;  119[aa];  Orientation:+3; 
Codon Adaptation Index (CAI). 0.852

Gene function information  Gene family PPI viewer Similarity Search Tool TACT
H-Inv ID HIT000101512
H-Inv cluster ID Locus viewHIX0033667
Accession number D49400.1
CAGE tag ID NA
EST ID NA
Transcript feature  Help NO; 
Coding potential  Help Protein coding; 
Definition V-type proton ATPase subunit F; V-ATPase subunit F; V-ATPase 14 kDa subunit; Vacuolar proton pump subunit F;
Similarity category  Help Category: Identical to known human protein(Category I).
Identical to known human protein (Q16864)  [Identity/coverage = 99.16%/100.0%] to Homo sapiens (Human). protein.
Experimental evidence Protein evidence
PubMed ID 85817361548933421269460ALL
Gene family/group Gene family H-Inv gene family/group ID HIF0002542
Gene family/group name ATPase, V1 complex, subunit F, eukaryotic (IPR005772).
Evidence motif (InterPro) ID IPR005772
Gene symbol/name HGNC symbol ATP6V1F
HGNC aliases NA
HGNC name ATPase, H+ transporting, lysosomal 14kDa, V1 subunit F
DDBJ NA
UniProt ATP6V1F
EC number EC 3.6.1.3adenosinetriphosphatase; 
GGDB
(GlycoGene Database)
Gene symbol NA
Familly NA
Designation NA
Expression NA
KEGG metabolic pathway 00230 :Purine metabolism; 
Protein-protein interaction (PPI) PPI viewer H-Inv protein ID HIP000027841
No. of interaction 13
Interaction partner(s) HIP000031904HIP000031904HIP000033722HIP000040212HIP000045212HIP000079362HIP000089323HIP000095593HIP000095593HIP000098362HIP000103276HIP000116600HIP000193291
BIND 180328;  301689;  301696;  301698;  301726; 
DIP NA
MINT MINT-8007070; 
HPRD 00783;  01967;  06120; 
IntAct NA
Database links RefSeq NM_004231NM_001198909
Ensembl ENST00000249289ENST00000492758
Entrez Gene Entrez Gene ID:9296
KEGG GENES KEGG GENES(9296)
GeneCard GeneCardATP6V1F*GeneCards is provided free to academic non-profit institutions.
etc H-GOLDHuman-Gene diversity Of Life-style related Diseases
Curation status Auto-annotated
Notes NA
Related H-InvDB links ATPase, V1 complex, subunit F, eukaryotic (IPR005772). Similarity Search ToolSimilarity Search Tool;  TACTTACT
fRNAdb (The functional RNA database) : overlapping fRNAdb entries with H-InvDB transcripts based on the location of the genome. 
NA


Subcellular localization information  Last modified:20-Apr-2012
WoLF PSORT cytosol;  nuclear;  cytoskeleton;  extracellular; 
Target P Other
SOSUI soluble protein
TMHMM soluble protein
PTS1 Not targeted
Related H-InvDB links LIFEdb LIFEdb; 
JRE-1.4.0 or later is required. Download JRE at Sun's web site.

Protein structure information (GTOP) GTOP Last modified:20-Apr-2012
Start End PDB_ID E-value Identity Coverage SCOP_ID
9 108 2d00A1 1e-25 20.5 88/104 c.149.1.1
Related H-InvDB links GTOP GTOP

Gene expression information  H-ANGEL DNAProbeLocator Last modified:20-Apr-2012
Tissue-specific expression  H-ANGEL NA
Probe
information DNAProbeLocator
AceGene AGhsA201222; 
Affymetrix
GeneChip
HG-Focus 201527_at; 
HG-U133 201527_at; 
HG-U133A 201527_at; 
HG-U133A_2 201527_at; 
HG-U133B NA
HG-U133_Plus_2 201527_at; 
HG-U95 37395_at; 
HG-U95A 37395_at; 
HG-U95B NA
HG-U95C NA
HG-U95D NA
HG-U95E NA
HG-U95Av2 NA
HuEx-1_0 3023213;  3023219;  3023220;  3413342; 
HuGeneFL D49400_at; 
Agilent Human 1A Oligo Microarray:PGID215 A_23_P93623; 
Whole Human Genome Oligo Microarray:PGID247 A_23_P93623; 
Related H-InvDB links H-ANGELH-ANGEL DNAProbeLocatorDNAProbeLocator

Disease/pathology information  DiseaseInfo Viewer LEGENDA Last modified:20-Apr-2012
Disease relation Disease name:NA
Related information in OMIM OMIM ID:NA Title:NA
Co-localized orphan diseases OMIM ID:  605635
Disease related mutation NA
Literature-Extracted GENe-Disease Associations (LEGENDA) LEGENDA Gene name Entrez Gene ID:(9296)
Disease Entrez Gene ID:(9296)
Substance Entrez Gene ID:(9296)
Related H-InvDB links DiseaseInfo ViewerDiseaseInfo ViewerLEGENDALEGENDA

Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information  VaryGene Repeat mask viewer
 Single Nucleotide Polymorphism (SNP) and indel  VaryGene
Location Variation dbSNP ID Strand CDS/UTR Translation
12 .. 12 C/T rs11547837 + 5'UTR
17 .. 17 G/T rs75593211 + 5'UTR
39 .. 39 C/T rs113816833 + 5'UTR
73 .. 73 C/T rs1804887 + CDS Nonsynonymous[Thr8Ile]
121 .. 121 G/T rs10958 + CDS Nonsynonymous[Gly24Val]
164 .. 164 G/C rs112994393 + CDS Synonymous[Val38Val]
288 .. 288 G/A rs73459264 + CDS Nonsynonymous[Ala80Thr]
309 .. 309 G/A rs11547835 + CDS Nonsynonymous[Ala87Thr]
339 .. 339 C/A rs11547836 + CDS Nonsynonymous[Pro97Thr]
393 .. 393 G/C rs1804889 + CDS Nonsynonymous[Ala115Pro]
442 .. 442 G/T rs1804888 + 3'UTR
551 .. 551 C/T rs1050684 + 3'UTR
601 .. 601 C/T rs3580 - 3'UTR
616 .. 616 C/T rs15498 + 3'UTR
 Microsatellite (Short Tandem Repeat, STR)
No data available
 Microsatellite: Human-Gene diversity Of Life-style related Diseases (H-GOLD)
No data available
 Repeat  Repeat mask viewer
No data available
Database links H-GOLDHuman-Gene diversity Of Life-style related Diseases(H-GOLD)
Related H-InvDB links VaryGeneVaryGene Repeat mask viewerRepeat Mask Viewer