ENSMUSG00000010936


Mus musculus

Features
Gene ID: ENSMUSG00000010936
  
Biological name :Vac14
  
Synonyms : Q80WQ2 / Vac14 / Vac14 homolog (S. cerevisiae)
  
Possible biological names infered from orthology : Q08AM6 / Vac14, PIKFYVE complex component
  
Species: Mus musculus
  
Chr. number: 8
Strand: 1
Band: D3
Gene start: 110618585
Gene end: 110720398
  
Corresponding Affymetrix probe sets: 10575476 (MoGene1.0st)   1416231_at (Mouse Genome 430 2.0 Array)   
  
Cross references: Ensembl peptide - ENSMUSP00000148440
Ensembl peptide - ENSMUSP00000148548
Ensembl peptide - ENSMUSP00000034190
NCBI entrez gene - 234729     See in Manteia.
MGI - MGI:2157980
RefSeq - XM_006530918
RefSeq - XM_006530919
RefSeq - NM_146216
RefSeq Peptide - NP_666328
swissprot - Q80WQ2
swissprot - A0A1D5RLY2
swissprot - A0A1D5RLN5
Ensembl - ENSMUSG00000010936
  
See expression report in BioGPS
See gene description in Wikigenes
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 vac14ENSDARG00000014303Danio rerio
 VAC14ENSGALG00000002458Gallus gallus
 VAC14ENSG00000103043Homo sapiens


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
No match


Protein motifs (from Interpro)
Interpro ID Name
 IPR011989  Armadillo-like helical
 IPR016024  Armadillo-type fold
 IPR021841  Vacuolar protein 14 C-terminal Fig4-binding domain
 IPR026825  Vacuole morphology and inheritance protein 14
 IPR032878  Vacuole morphology and inheritance protein 14, Fab1-binding region


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0006661 phosphatidylinositol biosynthetic process IEA
 biological_processGO:0006970 response to osmotic stress ISA
 biological_processGO:0042327 positive regulation of phosphorylation IEA
 cellular_componentGO:0005768 endosome IEA
 cellular_componentGO:0005774 vacuolar membrane ISA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0010008 endosome membrane IEA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0031090 organelle membrane IEA
 cellular_componentGO:0043231 intracellular membrane-bounded organelle IEA
 cellular_componentGO:0070772 PAS complex IEA
 molecular_functionGO:0005488 binding IEA
 molecular_functionGO:0019209 kinase activator activity ISA


Pathways (from Reactome)
Pathway description
Synthesis of PIPs at the Golgi membrane
Synthesis of PIPs at the early endosome membrane
Synthesis of PIPs at the late endosome membrane


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 MP:0000358 abnormal cell content/ morphology "structural anomalies of the minute protoplasmic masses that make up organized tissues and which are the fundamental structural and functional units of living organisms" [cwg:Carroll-Ann W. Goldsmith , Mouse Genome Informatics curator, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000371 diluted coat color "a coat color that appears lighter in intensity or paler than normal" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14ingls
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * DBA/2J

 MP:0000745 tremors "repetitive, cyclical movements of the body or a body part; usually involuntary, but can also manifest in response to an attempt at movement" [MeSH:National Library of Medicine - Medical Subject Headings , 2003, Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0000788 abnormal cerebral cortex morphology "malformed gray cellular mantle covering the surface of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:38857]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000807 abnormal hippocampus morphology "absent or malformed deep lying structure of the cerebrum involved with memory storage and spatial navigation" [The Atlas of Mouse Development:ISBN 0-12-402035-6, MGI:Cls, J:38857]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000819 abnormal olfactory bulb morphology "malformation or absence of the forebrain region that coordinates neuronal signaling involved in the perception of smell; it receives input from the sensory neurons and outputs to the olfactory cortex" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, Principles of Neural Science:ISBN 0-8385-8034-3, J:16461]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000832 abnormal thalamus morphology "malformation or absence of the large ovoid mass of paired bodies containing mostly gray matter and forming part of the lateral wall of the third ventricle of the brain" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000837 abnormal hypothalamus morphology "any malformation or absence of the ventral part of the diencephalon extending from the region of the optic chiasm to the caudal border of the mammillary bodies and forming the inferior and lateral walls of the third ventricle; this region regulates the autonomic nervous system via hormone production and release" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000846 abnormal medulla oblongata "anomaly in the most caudal region of the brainstem that lies directly rostral to the spinal cord; includes regions responsible for autonomic functions such as digestion, breathing and control of heart rate" [Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000848 abnormal pons "malformed band of nerve fibers in the brain connecting the medulla oblongata and the mesencephalon; this region conveys information about movement from the cerebral hemisphere to the cerebellum" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:1776, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000849 abnormal cerebellum morphology "any malformation or absence of the part of the metencephalon that lies in the posterior cranial fossa dorsal to the pons and medulla that is concerned with the coordination of movement and learning of motor skills" [J:50311, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000897 abnormal midbrain "malformation or malfunction associated with the middle of the three cerebral vesicles of the embryo; this region controls sensory and motor functions, including eye movement and coordination of auditory and visual reflexes" [J:23882, Principles of Neural Science , 3rd edition:ISBN 0-8385-8034-3]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000904 abnormal superior colliculus "dysmorphology or disorganization of the paired superior eminence of the mesencephalic tectum that is involved in auditory processing" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000960 abnormal sensory ganglia morphology "malformation or absence of a group of sensory neuron cell bodies" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:CLS, J:64962]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0000961 abnormal dorsal root ganglia morphology "malformed group of nerve cell bodies of each segmental nerve projecting from the spinal cord " [Stedman s Medical Dictionary:ISBN 0-683-40008-8, MGI:cls, J:60159]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0001092 abnormal trigeminal ganglion morphology "malformed group of sensory neuron cell bodies associated with the trigeminal nerve (fifth cranial nerve)" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:33038]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0001265 reduced body size "smaller than average body weight, height and/or length of an organism compared to controls" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, J:23170]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14ingls
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * DBA/2J

 MP:0001393 ataxia "inability to coordinate voluntary muscular movements" [Stedman s Medical Dictionary:ISBN 0-683-40008-8, J:67231]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0001516 abnormal motor coordination/ balance "altered ability of an animal to maintain skillful and effective interaction of movements or maintenance of equilibrium" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0001891 hydroencephaly "excessive accumulation of cerebrospinal fluid in the brain, especially the cerebral ventricles, often leading to increased brain size and other brain trauma" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, MeSH:National Library of Medicine - Medical Subject Headings, 2003]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0002152 abnormal brain morphology "anomalous structure of or abnormal development of the brain, one of the two components of the central nervous system and the center of thought and emotion; controls coordination, bodily activities and the interpretation of information from the senses (sight, hearing, smell, etc.)" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator, http://cancerweb.ncl.ac.uk]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0002183 gliosis "increased growth pattern of neuroglia in a damaged area of the brain or spinal cord" [Stedman s Medical Dictionary , 27th edition:ISBN 0-683-40008-8, csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0002654 spongiform encephalopathy "a neurodegenerative state characterized by the appearance of large vacuolated areas in the brain cells, resembling a sponge" [csmith:Cynthia L. Smith , Mouse Genome Informatics Curator]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0003105 abnormal heart atrium morphology "structural anomaly of one or both of the two upper chambers of the heart " [csmith:Cynthia L. Smith, Mouse Genome Informatics Curator]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0003354 astrocytosis "a proliferation or spread of astrocytes in the area of a degenerative lesion or damaged tissue" [MeSH:National Library of Medicine - Medical Subject Headings , 2003]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

 MP:0008535 enlarged lateral ventricles "increased size of the cavity in each of the cerebral hemispheres derived from the cavity of the embryonic neural tube; they are separated from each other by the septum pellucidum, and each communicates with the third ventricle by the foramen of Monro, through which also the choroid plexuses of the lateral ventricles become continuous with that of the third ventricle" [MESH:A08.186.211.276.650, MGI:csmith "Cynthia L. Smith, Mouse Genome Informatics Curator"]
Show

Allelic Composition: Eno2tm1(DTA)Hsak/?,Tg(Olfr16-cre,-ECFP)1Hsak/?
Genetic Background: involves: C57BL/6

 MP:0011085 complete postnatal lethality "premature death anytime between the neonatal period and weaning age of all organisms of a given genotype in a population (Mus: P1 to approximately 3 weeks of age)" [MGI:csmith]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14Gt(RRP155)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14ingls
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * DBA/2J

 MP:0011380 enlarged brain ventricle "increased size of one or more of the four communicating cavities within the brain that are continuous with the central canal of the spinal cord" [MGI:smb]
Show

Allelic Composition: Grid2Lc/Grid2+
Genetic Background: B6CBACa Aw-J/A-Grid2Lc/J

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14ingls
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J * DBA/2J

 MP:0012261 increased hindbrain apoptosis "increase in the number of cells of the hindbrain undergoing programmed cell death" [MGI:anna]
Show

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14Gt(RRP155)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0012503 increased midbrain apoptosis "increase in the number of cells of the midbrain undergoing programmed cell death" [MGI:anna]
Show

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14Gt(RRP155)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

 MP:0012504 increased forebrain apoptosis "increase in the number of cells of the forebrain undergoing programmed cell death" [MGI:anna]
Show

Allelic Composition: Vac14Gt(RRP155)Byg/Vac14Gt(RRP155)Byg
Genetic Background: involves: 129P2/OlaHsd * C57BL/6J

  


Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSMUSG00000025949 Q9Z1T6 / Pikfyve / phosphoinositide kinase, FYVE type zinc finger containing / Q9Y2I7*  / complex
 ENSMUSG00000038417 Fig4 / Q91WF7 / Polyphosphoinositide phosphatase / Q92562* / FIG4 phosphoinositide 5-phosphatase*  / complex






 

0 s.

 
External programs and data are copyrighted by and are the property of their respective authors.
The Manteia system, data and analyses are provided "as is" with no warranties, expressed or implied as to capabilities or accuracy. User assumes the entire risk as to the results and performance of the software, data and documentation


                   


© Olivier Tassy / Olivier Pourquie 2007-2024
contact: otassy@igbmc.fr