H-InvDB_8.3 released on March 26, 2013.
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H-Inv ID (HIT)
H-Inv cluster ID (HIX)
H-Inv protein ID (HIP)
H-Inv gene family/group (HIF)
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Chromosome number
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Definition*
Data source ID
---
CCDS ID
dbSNP ID (rs number)
EC number
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FR ID
FR Accession number
GO ID
GO name*
HGNC gene symbol
HGNC gene name*
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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;
Select format
Flat file
XML file
Nucleotide sequence fasta
Protein sequence fasta
Transcript original information
Accession number
D49400.1
CAGE tag ID
NA
EST ID
NA
Clone Number
NA
Experimental resources
NBRC
;
HGPD
;
Antibody (ATP6V1F)
;
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
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
AGTTTCAGTGGCTTCTGGTGCTCTAGGGTGAGCTCTGCCCGGCTGCAGGG ATGGCGGGGAGGGGTAAGCTCACCGCAGTGATCGGAGACGAGGACACGGT GACTGGTTTCCTGCTGGGCGGCATAGGGGAGCTTAACAAGAACCGCCATC CCAATTTCCTGGTGGTGGAGAAGGATACAACCATCAATGAGATCGAAGAC ACTTTCCGGCAATTTCTAAACCGGGATGACATTGGCATCATCCTCATCAA CCAGTACATCGCAGAGATGGTGCGGCATGCCCTGGACGCCCACCAGCAGT CCATCCCCGCTGTCCTGGAGATCCCCTCCAAGGAGCACCCATATGACGCC GCCAAGGACTCCATCCTGCGCAGGGCCAGGGGCATGTTCACTGCCGAAGA CCTGCGCTAGGGGACTCCTCATAGCCCTCAGCCCTTCCCTCGTTTCCAGG CCTCTCCCCAGGCTTGCCATCAGCCTTCTTTACTTTTTGAGCCTCTGATT TCCAATTCCCTGCTCCTTCCCACTCCATTAAGAGGCTAGGTGAGGCGCTT CTAGGTTGCTGGGGCTCTGCTGGTTAAGGAACAGGAAGCCTGACCATCTC CCTCCACTACCTCTTCCCTGTGCTGTTACACAGTGTCATTGTTGATGTTA AATTAAAGTCATATTCTTGCTTCTCTCCAG
Gene structure information
H-Inv cluster ID
HIX0033667
Genomic location
Chromosome
7
Location
7q32.1
Position
128502910- 128505902
Strand
+
Possible duplicated location(s)
NA
Gene structure
2 exon(s)
Database links
RefSeq
NM_004231
;
NM_001198909
;
Ensembl
ENST00000249289
;
ENST00000492758
;
Entrez Gene
Entrez Gene ID:9296
;
KEGG GENES
KEGG GENES(9296)
;
GeneCard
ATP6V1F
;
*GeneCards is provided free to academic non-profit institutions.
Related H-InvDB links
H-DBAS;
G-integra
;
cDNA-genome alignment
;
Predicted CDS information
HIP ID
HIP000027841
Predicted CDS
51..410; 119[aa]; Orientation:+3;
Codon Adaptation Index (CAI).
0.852
MAGRGKLTAVIGDEDTVTGFLLGGIGELNKNRHPNFLVVEKDTTINEIED TFRQFLNRDDIGIILINQYIAEMVRHALDAHQQSIPAVLEIPSKEHPYDA AKDSILRRARGMFTAEDLR*
Gene function information
H-Inv ID
HIT000101512
H-Inv cluster ID
HIX0033667
Accession number
D49400.1
CAGE tag ID
NA
EST ID
NA
Transcript feature
NO;
Coding potential
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
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
8581736
;
15489334
;
21269460
;
ALL
;
Gene family/group
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 3.6.1.3
adenosinetriphosphatase;
GGDB
(GlycoGene Database)
Gene symbol
NA
Familly
NA
Designation
NA
Expression
NA
KEGG metabolic pathway
00230
:Purine metabolism;
Protein-protein interaction (PPI)
H-Inv protein ID
HIP000027841
No. of interaction
13
Interaction partner(s)
HIP000031904
;
HIP000031904
;
HIP000033722
;
HIP000040212
;
HIP000045212
;
HIP000079362
;
HIP000089323
;
HIP000095593
;
HIP000095593
;
HIP000098362
;
HIP000103276
;
HIP000116600
;
HIP000193291
;
BIND
180328; 301689; 301696; 301698; 301726;
DIP
NA
MINT
MINT-8007070;
HPRD
00783; 01967; 06120;
IntAct
NA
Database links
RefSeq
NM_004231
;
NM_001198909
;
Ensembl
ENST00000249289
;
ENST00000492758
;
Entrez Gene
Entrez Gene ID:9296
;
KEGG GENES
KEGG GENES(9296)
;
GeneCard
ATP6V1F
;
*GeneCards is provided free to academic non-profit institutions.
etc
Human-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 Tool;
TACT
;
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;
JRE-1.4.0 or later is required.
Download JRE at
Sun's web site.
Protein structure information (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
Gene expression information
Last modified:20-Apr-2012
Tissue-specific expression
NA
Probe
information
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-ANGEL
;
DNAProbeLocator
;
Disease/pathology information
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)
Gene name
Entrez Gene ID:(9296)
Disease
Entrez Gene ID:(9296)
Substance
Entrez Gene ID:(9296)
Related H-InvDB links
DiseaseInfo Viewer
;
LEGENDA
;
Polymorphism (SNP, indel), microsatellite (Short Tandem Repeat, STR) and repeat information
Single Nucleotide Polymorphism (SNP) and indel
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
No data available
Database links
Human-Gene diversity Of Life-style related Diseases(H-GOLD)
;
Related H-InvDB links
VaryGene
;
Repeat Mask Viewer
;