ENSG00000154277


Homo sapiens

Features
Gene ID: ENSG00000154277
  
Biological name :UCHL1
  
Synonyms : P09936 / ubiquitin C-terminal hydrolase L1 / UCHL1
  
Possible biological names infered from orthology :
  
Species: Homo sapiens
  
Chr. number: 4
Strand: 1
Band: p13
Gene start: 41256413
Gene end: 41268455
  
Corresponding Affymetrix probe sets: 1555834_at (Human Genome U133 Plus 2.0 Array)   201387_s_at (Human Genome U133 Plus 2.0 Array)   
  
Cross references: Ensembl peptide - ENSP00000284440
Ensembl peptide - ENSP00000422542
Ensembl peptide - ENSP00000426895
Ensembl peptide - ENSP00000426634
Ensembl peptide - ENSP00000425714
Ensembl peptide - ENSP00000423623
Ensembl peptide - ENSP00000423348
NCBI entrez gene - 7345     See in Manteia.
OMIM - 191342
RefSeq - NM_004181
RefSeq Peptide - NP_004172
swissprot - D6RE83
swissprot - D6R974
swissprot - D6R956
swissprot - P09936
swissprot - D6RJD9
swissprot - V9HW74
swissprot - D6RF53
Ensembl - ENSG00000154277
  
Related genetic diseases (OMIM): 613643 - {?Parkinson disease 5, susceptibility to}, 613643
  615491 - Spastic paraplegia 79, autosomal recessive, 615491
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
 uchl1ENSDARG00000026871Danio rerio
 UCHL1ENSGALG00000014261Gallus gallus
 Uchl1ENSMUSG00000029223Mus musculus


Paralog prediction (from Ensembl)
Paralog nameIDSimilarity(%)
UCHL3 / P15374 / ubiquitin C-terminal hydrolase L3ENSG0000011893955


Protein motifs (from Interpro)
Interpro ID Name
 IPR001578  Peptidase C12, ubiquitin carboxyl-terminal hydrolase
 IPR030297  Ubiquitin carboxyl-terminal hydrolase L1
 IPR036959  Peptidase C12, ubiquitin carboxyl-terminal hydrolase superfamily


Gene Ontology (GO)
TypeGO IDTermEv.Code
 biological_processGO:0002931 response to ischemia IEA
 biological_processGO:0006508 proteolysis IEA
 biological_processGO:0006511 ubiquitin-dependent protein catabolic process IEA
 biological_processGO:0007409 axonogenesis IEA
 biological_processGO:0007412 axon target recognition IEA
 biological_processGO:0007628 adult walking behavior IEA
 biological_processGO:0008283 cell proliferation IEA
 biological_processGO:0016241 regulation of macroautophagy TAS
 biological_processGO:0016579 protein deubiquitination IEA
 biological_processGO:0019233 sensory perception of pain IEA
 biological_processGO:0019896 axonal transport of mitochondrion IEA
 biological_processGO:0042755 eating behavior IEA
 biological_processGO:0043161 proteasome-mediated ubiquitin-dependent protein catabolic process NAS
 biological_processGO:0043407 negative regulation of MAP kinase activity IDA
 biological_processGO:0048747 muscle fiber development IEA
 biological_processGO:0050905 neuromuscular process IEA
 cellular_componentGO:0005622 intracellular IEA
 cellular_componentGO:0005654 nucleoplasm IDA
 cellular_componentGO:0005737 cytoplasm IDA
 cellular_componentGO:0005783 endoplasmic reticulum IEA
 cellular_componentGO:0005789 endoplasmic reticulum membrane IEA
 cellular_componentGO:0005829 cytosol IDA
 cellular_componentGO:0005886 plasma membrane IDA
 cellular_componentGO:0016020 membrane IEA
 cellular_componentGO:0030424 axon IEA
 cellular_componentGO:0043025 neuronal cell body IEA
 cellular_componentGO:0043209 myelin sheath IEA
 cellular_componentGO:0044306 neuron projection terminus IEA
 cellular_componentGO:0070062 extracellular exosome HDA
 cellular_componentGO:1904115 axon cytoplasm IEA
 molecular_functionGO:0004197 cysteine-type endopeptidase activity IDA
 molecular_functionGO:0004843 thiol-dependent ubiquitin-specific protease activity IEA
 molecular_functionGO:0005515 protein binding IPI
 molecular_functionGO:0008233 peptidase activity IEA
 molecular_functionGO:0008234 cysteine-type peptidase activity IEA
 molecular_functionGO:0008242 omega peptidase activity IDA
 molecular_functionGO:0016787 hydrolase activity IEA
 molecular_functionGO:0016874 ligase activity IEA
 molecular_functionGO:0031625 ubiquitin protein ligase binding IPI
 molecular_functionGO:0031694 alpha-2A adrenergic receptor binding IPI
 molecular_functionGO:0036459 thiol-dependent ubiquitinyl hydrolase activity IEA
 molecular_functionGO:0043130 ubiquitin binding IEA


Pathways (from Reactome)
Pathway description
UCH proteinases


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:0000529 Progressive visual loss 
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 HP:0000545 Myopia 
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 HP:0000639 Nystagmus "Rhythmic, involuntary oscillations of one or both eyes related to abnormality in fixation, conjugate gaze, or vestibular mechanisms." [HPO:curators]
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 HP:0000648 Optic atrophy 
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 HP:0001258 Spastic paraplegia 
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 HP:0001272 Cerebellar atrophy 
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 HP:0001310 Dysmetria 
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 HP:0001371 Contractures 
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 HP:0001761 Pes cavus 
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 HP:0001763 Pes planus "A condition in which the arch of the foot is flat, with the entire sole of the foot being in near-complete contact with the ground." [HPO:curators]
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 HP:0002059 Cerebral atrophy 
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 HP:0002080 Intention tremor "An oscillatory cerebellar ataxia that tends to be absent when the limbs are inactive and during the first part of voluntary movement but worsening as the movement continues and greater precision is required (e.g., in touching a target such as the patient s nose or a physician s finger)." [HPO:curators]
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 HP:0002180 Neurodegeneration 
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 HP:0002273 Tetraparesis 
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 HP:0002380 Fasciculations "Fasciculations are observed as small, local, involuntary muscle contractions (twitching) visible under the skin. Fasciculations result from increased irritability of an axon (which in turn is often a manifestation of disease of a motor neuron). This leads to sporadic discharges of all the muscle fibers controlled by the axon in isolation from other motor units." [HPO:curators]
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 HP:0002411 Myokymia 
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 HP:0002486 Myotonia "Myotonia is characterized by an abnormally slow relaxation of the muscles after voluntary contraction or electrical stimulation. During physical examination, myotonia may be elicited by asking the patient to make a tight fist and then quickly open the hand." [HPO:curators]
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 HP:0002599 Head titubation 
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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:0003676 Progressive disorder 
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 HP:0011448 Ankle clonus "Clonus is an involuntary tendon reflex that causes repeated flexion and extension of the foot. Ankle clonus is tested by rapidly flexing the foot upward." [HPO:probinson]
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Interacting proteins (from Reactome)
Interactor ID Name Interaction type
No match






 

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