ENSG00000100225


Homo sapiens

Features
Gene ID: ENSG00000100225
  
Biological name :FBXO7
  
Synonyms : F-box protein 7 / FBXO7 / Q9Y3I1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 22
Strand: 1
Band: q12.3
Gene start: 32474676
Gene end: 32498829
  
Corresponding Affymetrix probe sets: 1554423_a_at (Human Genome U133 Plus 2.0 Array)   201178_at (Human Genome U133 Plus 2.0 Array)   243649_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000404388
Ensembl peptide - ENSP00000395823
Ensembl peptide - ENSP00000406155
Ensembl peptide - ENSP00000266087
Ensembl peptide - ENSP00000380571
Ensembl peptide - ENSP00000388547
NCBI entrez gene - 25793     See in Manteia.
OMIM - 605648
RefSeq - XM_011530106
RefSeq - NM_001033024
RefSeq - NM_001257990
RefSeq - NM_012179
RefSeq Peptide - NP_001244919
RefSeq Peptide - NP_001028196
RefSeq Peptide - NP_036311
swissprot - Q9Y3I1
swissprot - F8WBR0
swissprot - A2A282
swissprot - F8WDR9
Ensembl - ENSG00000100225
  
Related genetic diseases (OMIM): 260300 - Parkinson disease 15, autosomal recessive, 260300
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
 fbxo7ENSDARG00000099833Danio rerio
 FBXO7ENSGALG00000012569Gallus gallus
 Fbxo7ENSMUSG00000001786Mus musculus


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


Protein motifs (from Interpro)
Interpro ID Name
 IPR001810  F-box domain
 IPR021625  PI31 proteasome regulator, N-terminal
 IPR029071  Ubiquitin-like domain superfamily
 IPR036047  F-box-like domain superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0000209 protein polyubiquitination TAS
 biological_processGO:0000422 autophagy of mitochondrion IMP
 biological_processGO:0006511 ubiquitin-dependent protein catabolic process IDA
 biological_processGO:0006626 protein targeting to mitochondrion IMP
 biological_processGO:0010975 regulation of neuron projection development IMP
 biological_processGO:0016567 protein ubiquitination IDA
 biological_processGO:0031647 regulation of protein stability IDA
 biological_processGO:0040012 regulation of locomotion IDA
 biological_processGO:0043687 post-translational protein modification TAS
 biological_processGO:0045620 negative regulation of lymphocyte differentiation IEA
 biological_processGO:0045736 negative regulation of cyclin-dependent protein serine/threonine kinase activity IEA
 biological_processGO:1901215 negative regulation of neuron death IEA
 biological_processGO:1903204 negative regulation of oxidative stress-induced neuron death IMP
 biological_processGO:1903599 positive regulation of autophagy of mitochondrion IEA
 biological_processGO:2000134 negative regulation of G1/S transition of mitotic cell cycle IEA
 cellular_componentGO:0000151 ubiquitin ligase complex IDA
 cellular_componentGO:0005634 nucleus IEA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005739 mitochondrion IEA
 cellular_componentGO:0005829 cytosol TAS
 cellular_componentGO:0019005 SCF ubiquitin ligase complex TAS
 cellular_componentGO:0032991 protein-containing complex IDA
 cellular_componentGO:0097409 glial cytoplasmic inclusion IDA
 cellular_componentGO:0097414 classical Lewy body IDA
 cellular_componentGO:0097462 Lewy neurite IDA
 cellular_componentGO:1990037 Lewy body core IDA
 cellular_componentGO:1990038 Lewy body corona IDA
 molecular_functionGO:0004842 ubiquitin-protein transferase activity EXP
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0019901 protein kinase binding IEA
 molecular_functionGO:0031625 ubiquitin protein ligase binding IPI
 molecular_functionGO:0043130 ubiquitin binding IDA
 molecular_functionGO:0046982 protein heterodimerization activity IPI


Pathways (from Reactome)
Pathway description
Neddylation
Antigen processing: Ubiquitination & Proteasome degradation


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:0000514 Slow saccades 
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 HP:0001260 Dysarthria "Dysarthric speech is a general description referring to a neurological speech disorder characterized by poor articulation. Depending on the involved neurological structures, dysarthria may be further classified as spastic, flaccid, ataxic, hyperkinetic and hypokinetic, or mixed." [HPO:curators]
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 HP:0001332 Dystonia "An abnormally increased muscular tone that causes fixed abnormal postures. There is a slow, intermittent twisting motion that leads to exaggerated turning and posture of the extremities and trunk." [HPO:curators]
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 HP:0001337 Tremor "An unintentional, oscillating to-and-fro muscle movement." [HPO:curators]
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 HP:0001347 Hyperreflexia "The presence of overactive or overresponsive reflexes." [HPO:curators]
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 HP:0001762 Talipes equinovarus "Also called clubfoot typically has 4 main components: inversion and adduction of the forefoot; inversion of the heel and hindfoot; equinus (limitation of extension) of the ankle and subtalar joint; and internal rotation of the leg. Clubfoot is a complex, multifactorial deformity with genetic and intrauterine factors. One popular theory postulates that a clubfoot is a result of intrauterine maldevelopment of the talus that leads to adduction and plantarflexion of the foot. On radiographic projection a clubfoot can be noted as parallel axes of talus and calcaneus." [HPO:curators]
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 HP:0002061 Lower limb spasticity 
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 HP:0002063 Rigidity 
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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:0002071 Extrapyramidal signs 
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 HP:0002172 Postural instability 
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 HP:0002548 Favorable response to levodopa 
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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:0003677 Slow progression 
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 HP:0011462 Young adult onset "Onset of disease at the age of between 15 and 40 years." [DDD:hfirth]
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 HP:0012407 Scissor gait "A form of gait abnormality characterized by hypertonia and flexion in the legs, hips and pelvis accompanied by extreme adduction leading to the knees and thighs hitting, or sometimes even crossing, in a scissors-like movement. The opposing muscles (abductors) become comparatively weak from lack of use." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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