ENSG00000182220


Homo sapiens

Features
Gene ID: ENSG00000182220
  
Biological name :ATP6AP2
  
Synonyms : ATP6AP2 / ATPase H+ transporting accessory protein 2 / O75787
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: X
Strand: 1
Band: p11.4
Gene start: 40579372
Gene end: 40606848
  
Corresponding Affymetrix probe sets: 201442_s_at (Human Genome U133 Plus 2.0 Array)   201443_s_at (Human Genome U133 Plus 2.0 Array)   201444_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000490462
Ensembl peptide - ENSP00000367697
Ensembl peptide - ENSP00000403969
Ensembl peptide - ENSP00000410105
Ensembl peptide - ENSP00000411317
Ensembl peptide - ENSP00000489622
Ensembl peptide - ENSP00000489653
Ensembl peptide - ENSP00000489819
Ensembl peptide - ENSP00000489845
Ensembl peptide - ENSP00000489920
Ensembl peptide - ENSP00000490083
Ensembl peptide - ENSP00000490239
Ensembl peptide - ENSP00000490257
Ensembl peptide - ENSP00000490345
Ensembl peptide - ENSP00000490382
Ensembl peptide - ENSP00000490452
Ensembl peptide - ENSP00000490532
Ensembl peptide - ENSP00000490558
Ensembl peptide - ENSP00000490675
Ensembl peptide - ENSP00000490706
Ensembl peptide - ENSP00000490733
Ensembl peptide - ENSP00000490884
Ensembl peptide - ENSP00000490954
NCBI entrez gene - 10159     See in Manteia.
OMIM - 300556
RefSeq - NM_005765
RefSeq Peptide - NP_005756
swissprot - A0A1B0GTU8
swissprot - A0A1B0GU12
swissprot - A0A1B0GUT7
swissprot - A0A1B0GUV3
swissprot - A0A1B0GV24
swissprot - A0A1B0GV60
swissprot - A0A1B0GVB9
swissprot - A0A1B0GVC7
swissprot - A0A1B0GVI9
swissprot - A0A1B0GVW0
swissprot - A0A1B0GVZ1
swissprot - A0A1B0GW13
swissprot - A0A1B0GWD6
swissprot - A0A1B0GWJ8
swissprot - A0A1C7CYW4
swissprot - B7Z1I9
swissprot - B7Z413
swissprot - H7C240
swissprot - H7C3E1
swissprot - O75787
swissprot - A0A1B0GTB0
swissprot - A0A1B0GTD6
Ensembl - ENSG00000182220
  
Related genetic diseases (OMIM): 300423 - Mental retardation, X-linked, syndromic, Hedera type, 300423
  300911 - ?Parkinsonism with spasticity, X-linked, 300911
See expression report in BioGPS
See gene description in Wikigenes
See gene description in GeneCards
See co-cited genes in PubMed


Ortholog prediction (from Ensembl)
Ortholog nameID Species
 atp6ap2ENSDARG00000008735Danio rerio
 ATP6AP2ENSGALG00000016241Gallus gallus
 Q9CYN9ENSMUSG00000031007Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR012493  Renin receptor-like
 IPR017850  Alkaline-phosphatase-like, core domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002003 angiotensin maturation TAS
 biological_processGO:0008152 metabolic process IEA
 biological_processGO:0021903 rostrocaudal neural tube patterning IMP
 biological_processGO:0030177 positive regulation of Wnt signaling pathway IMP
 biological_processGO:0032914 positive regulation of transforming growth factor beta1 production IDA
 biological_processGO:0043312 neutrophil degranulation TAS
 biological_processGO:0043408 regulation of MAPK cascade IDA
 biological_processGO:0048069 eye pigmentation IMP
 biological_processGO:0060323 head morphogenesis IMP
 cellular_componentGO:0005886 plasma membrane TAS
 cellular_componentGO:0009897 external side of plasma membrane IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0016021 integral component of membrane IEA
 cellular_componentGO:0043005 neuron projection IEA
 cellular_componentGO:0044297 cell body IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:0070821 tertiary granule membrane TAS
 cellular_componentGO:0101003 ficolin-1-rich granule membrane TAS
 molecular_functionGO:0003824 catalytic activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0019899 enzyme binding IEA


Pathways (from Reactome)
Pathway description
Metabolism of Angiotensinogen to Angiotensins
Neutrophil degranulation


Phenotype (from MGI, Zfin or HPO)
IDPhenotypeDefinition Genetic BG
 HP:0000007 Autosomal recessive inheritance "A mode of inheritance that is observed for traits related to a gene encoded on one of the autosomes (i.e., the human chromosomes 1-22) in which a trait manifests in homozygotes. In the context of medical genetics, autosomal recessive disorders manifest in homozygotes (with two copies of the mutant allele) or compound heterozygotes (whereby each copy of a gene has a distinct mutant allele)." [HPO:curators]
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 HP:0000338 Hypomimic face 
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 HP:0000750 Impaired language development 
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 HP:0001249 Mental retardation 
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 HP:0001257 Spasticity "A motor disorder characterized by a velocity-dependent increase in tonic stretch reflexes with increased muscle tone, exaggerated (hyperexcitable) tendon reflexes." [HPO:curators]
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 HP:0001265 Hyporeflexia 
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 HP:0001270 Motor retardation 
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 HP:0001272 Cerebellar atrophy 
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 HP:0001288 Gait disturbance "The term gait disturbance can refer to any disruption of the ability to walk. In general, this can refer to neurological diseases but also fractures or other sources of pain that is triggered upon walking. However, in the current context gait disturbance refers to difficulty walking on the basis of a neurological or muscular disease." [HPO:curators]
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 HP:0001300 Parkinsonism 
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0001419 X-linked recessive inheritance "A mode of inheritance that is observed for recessive traits related to a gene encoded on the X chromosome. In the context of medical genetics, X-linked recessive disorders manifest in males (who have one copy of the X chromosome and are thus hemizygotes), but generally not in female heterozygotes who have one mutant and one normal allele." [HPO:curators]
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 HP:0002059 Cerebral atrophy 
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 HP:0002067 Bradykinesia "Bradykinesia literally means slow movement, and is used clinically to denote a slowness in the execution of movement (in contrast to hypokinesia, which is used to refer to slowness in the initiation of movement)." [HPO:curators]
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 HP:0002069 Generalized tonic-clonic seizures "Generalized tonic-clonic seizures are `generalized seizures` (HP:0002197) in which the patient suddenly loses conciousness, the eyes roll back, and the entire body musculature undergoes tonic contractions. In the clonic phase of the seizure, there are rhythmic contractions of the musculature alternating with relaxation of all muscle groups. Loss of sphincter control during the seizure is common. This form of seizure was formerly commonly called grand mal seizure." [HPO:curators]
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 HP:0002079 Hypoplasia of the corpus callosum "Underdevelopment of the corpus callosum." [HPO:curators]
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 HP:0002322 Resting tremor "A resting tremor occurs when muscles are at rest and becomes less noticeable or disappears when the affected muscles are moved. Resting tremors are often slow and coarse." [HPO:curators]
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 HP:0002345 Action tremor "A tremor present when the limbs are active, either when outstretched in a certain position or throughout a voluntary movement." [HPO:curators]
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 HP:0002396 Cogwheel rigidity 
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 HP:0003487 Babinski sign "Upturning of the big toe (and sometimes fanning of the other toes) in response to stimulation of the sole of the foot. If the Babinski sign is present it can indicate damage to the corticospinal tract." [HPO:curators]
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 HP:0003593 Early onset 
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 HP:0003677 Slow progression 
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 HP:0003828 Variable expressivity 
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 HP:0010527 Astereognosia "Inability to recognize the form of objects by touch based on the texture, size, weight and three-dimensional form of the object in the absence of any major somatosensory deficit." [HPO:curators]
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 HP:0011812 Agraphesthesia "Impaired ability to recognize letters or numbers drawn by an examiner s fingertip on the patient s skin (the patients eyes are closed or covered throughout this examination)." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
 ENSG00000143839 REN / renin / P00797  / complex






 

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contact: otassy@igbmc.fr