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Atp6v1b2 Gene Detail
Summary
  • Symbol
    Atp6v1b2
  • Name
    ATPase, H+ transporting, lysosomal V1 subunit B2
  • Synonyms
    Atp6b2, HO57
  • Feature Type
    protein coding gene
  • IDs
    MGI:109618
    NCBI Gene: 11966
  • Alliance
  • Transcription Start Sites
    7 TSS
Location &
Maps
more
  • Sequence Map
    Chr8:69541388-69566370 bp, + strand
    From NCBI annotation of GRCm39
  • View this region in JBrowse
  • Genome Browsers
  • Genetic Map
    Chromosome 8, 33.88 cM
  • Mapping Data
    1 experiment
Strain
Comparison
more
  • SNPs within 2kb
    695 from dbSNP Build 142
  • Strain Annotations
    19
For selected strains:
Strain Gene Model ID Feature Type Coordinates Select Strains
C57BL/6J MGI_C57BL6J_109618
protein coding gene Chr8:69541298-69566370 (+)
129S1/SvImJ ENSMUSG00200031912
protein coding gene Chr8:64384734-64409835 (+)
A/J ENSMUSG00195014348
protein coding gene Chr8:64795205-64820264 (+)
AKR/J ENSMUSG00220022085
protein coding gene Chr8:64626060-64650938 (+)
BALB/cJ ENSMUSG00180025675
protein coding gene Chr8:64359387-64384495 (+)
C3H/HeJ ENSMUSG00175019980
protein coding gene Chr8:64622699-64647576 (+)
C57BL/6NJ ENSMUSG00215023440
protein coding gene Chr8:64368212-64393279 (+)
CAROLI/EiJ MGP_CAROLIEiJ_G0031107
protein coding gene Chr8:61316302-61341035 (+)
CAST/EiJ ENSTCUG00005035747
protein coding gene Chr8:64132419-64157690 (+)
CBA/J ENSMUSG00210028881
protein coding gene Chr8:64506874-64531694 (+)
DBA/2J ENSMUSG00185021914
protein coding gene Chr8:70554753-70579628 (+)
FVB/NJ ENSMUSG00205025321
protein coding gene Chr8:63910740-63935848 (+)
JF1/MsJ ENSUMUG00000012470
protein coding gene Chr8:72797547-72822599 (+)
LP/J ENSMUSG00230031638
protein coding gene Chr8:74176181-74201834 (+)
NOD/ShiLtJ ENSMUSG00190025267
protein coding gene Chr8:64411721-64436782 (+)
NZO/HlLtJ ENSMUSG00225045809
protein coding gene Chr8:77594788-77620233 (+)
PWK/PhJ ENSLUMG00010032649
protein coding gene Chr8:64261328-64286362 (+)
SPRET/EiJ ENSMSPG00010038932
protein coding gene Chr8:65662207-65687277 (+)
WSB/EiJ ENSIUOG00005025337
protein coding gene Chr8:65196300-65221565 (+)



Homology
more
  • Human Ortholog
    ATP6V1B2, ATPase H+ transporting V1 subunit B2
  • Vertebrate Orthologs
    4
Vertebrate Orthology Source
Alliance of Genome Resources
  • Human Ortholog
    ATP6V1B2, ATPase H+ transporting V1 subunit B2
  • Synonyms
    ATP6B1B2, ATP6B2, DOOD, HO57, VATB, Vma2, VPP3, ZLS2
  • Links
    NCBI Gene ID: 526
    UniProt: P21281

  • Chr Location
    8p21.3; chr8:20197381-20230399 (+)  GRCh38

Human Diseases
more
  • Diseases
    2 with Atp6v1b2 mouse models; 1 with human ATP6V1B2 associations

Human Disease Mouse Models
      
IDs
View 2 models
      
IDs
View 1 model
Click on a disease name to see all genes associated with that disease.

  • Mutations/Alleles
    2 with disease annotations
  • References
    2 with disease annotations
Mutations,
Alleles, and
Phenotypes
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  • Phenotype Summary
    26 phenotypes from 3 alleles in 3 genetic backgrounds
    15 phenotype references
Phenotype Overview

adipose tissue
behavior/neurological
cardiovascular system
cellular
craniofacial
digestive/alimentary system
embryo
endocrine/exocrine glands
growth/size/body
hearing/vestibular/ear
hematopoietic system
homeostasis/metabolism
integument
immune system
limbs/digits/tail
liver/biliary system
mortality/aging
muscle
nervous system
pigmentation
renal/urinary system
reproductive system
respiratory system
skeleton
taste/olfaction
neoplasm
vision/eye

Click cells to view annotations.
Mice homozygous for a single point mutation show slow postnatal weight gain, abnormal hippocampus CA1 region morphology, cognitive deficits, and environmentally induced seizures. Homozygosity for the p.R506* mutation leads to hyperactivity, decreased anxiety, lower chemically induced seizure threshold and stimuli-induced seizures.
Gene Ontology
(GO)
Classifications
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  • All GO Annotations
  • GO References
Molecular Function

carbohydrate derivative binding
cytoskeletal protein binding
DNA binding
enzyme regulator
hydrolase
ligase
lipid binding
oxidoreductase
RNA binding
signaling receptor activity
signaling receptor binding
transcription
transferase
transporter
Biological Process

carbohydrate derivative metabolism
cell differentiation
cell population proliferation
cellular component organization
DNA-templated transcription
establishment of localization
homeostatic process
immune system process
lipid metabolic process
programmed cell death
protein metabolic process
response to stimulus
signaling
system development
Cellular Component

cell projection
cytoplasmic vesicle
cytoskeleton
cytosol
endoplasmic reticulum
endosome
extracellular region
Golgi apparatus
mitochondrion
membraneless organelle
nucleus
organelle envelope
organelle lumen
plasma membrane
protein-containing complex
synapse
vacuole
Click cells to view annotations.
Expression
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Expression Overview

early conceptus
embryo ectoderm
embryo endoderm
embryo mesoderm
embryo mesenchyme
extraembryonic component
alimentary system
auditory system
branchial arches
cardiovascular system
connective tissue
endocrine system
exocrine system
hemolymphoid system
integumental system
limbs
liver and biliary system
musculoskeletal system
nervous system
olfactory system
reproductive system
respiratory system
urinary system
visual system
Click cells to view annotations.


  • Assay Results
  • Tissues
  • cDNA Data
  • Literature Summary
  • Comparison Matrix
  • Sequences &
    Gene Models
    less
    Representative SequencesLengthStrain/SpeciesFlank
    genomic 11966 NCBI Gene Model | MGI Sequence Detail 24983 C57BL/6J ±  kb
    transcript NM_007509 RefSeq | MGI Sequence Detail 2742 C57BL/6  
    polypeptide P62814 UniProt | EBI | MGI Sequence Detail 511 Not Applicable  
    For the selected sequence
    Protein
    Information
    less
    • UniProt
      3 Sequences
    • Protein Ontology
      PR:000004482 V-type proton ATPase subunit B, brain isoform
    • PDB
    • EC
    • InterPro Domains
      IPR020003 ATPase, alpha/beta subunit, nucleotide-binding domain, active site
      IPR004100 ATPase, F1/V1/A1 complex, alpha/beta subunit, N-terminal domain
      IPR000194 ATPase, F1/V1/A1 complex, alpha/beta subunit, nucleotide-binding domain
      IPR005723 ATPase, V1 complex, subunit B
      IPR055190 ATP synthase A/B type, C-terminal domain
      IPR027417 P-loop containing nucleoside triphosphate hydrolase
      IPR022879 V-type ATP synthase regulatory subunit B/beta
    • GlyGen
      P62814 2 sites, 1 N-linked glycan (1 site), 1 O-linked glycan (1 site)
    Molecular
    Reagents
    less
    • All nucleic 465
      cDNA 459
      Primer pair 5
      Other 1
      Antibodies 2

      Microarray probesets 7
    Other
    Accession IDs
    less
    MGD-MRK-39617, MGI:2142474, MGI:2142617, MGI:2142893
    References
    more
    • Summaries
      All 82
      Developmental Gene Expression 19
      Diseases 2
      Gene Ontology 20
      Phenotypes 15
    • Earliest
      J:20867 van Hille B, et al., Heterogeneity of vacuolar H(+)-ATPase: differential expression of two human subunit B isoforms. Biochem J. 1994 Oct 1;303(Pt 1):191-8
    • Latest
      J:390120 Trowe MO, et al., Mesenchymal WNT signaling coordinates epithelial and mesenchymal differentiation in the developing murine ureter. Cell Commun Signal. 2026 Jul 21;24(1)

    Contributing Projects:
    Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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    last database update
    09/01/2026
    MGI 6.24
    The Jackson Laboratory