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Uchl1
Gene Detail
 Symbol
Name
ID
Uchl1
ubiquitin carboxy-terminal hydrolase L1
MGI:103149
Synonyms PGP 9.5, PGP9.5
Feature Type protein coding gene
Genetic Map
Chromosome 5
35.95 cM
Detailed Genetic Map ± 1 cM


Mapping data(7)
Sequence Map
Chr5:66676098-66687231 bp, + strand
From VEGA annotation of GRCm38

  11134 bp   ±  kb flank

VEGA Genome Browser | Ensembl Genome Browser | UCSC Browser | NCBI Map Viewer


Mouse Genome Browser
Vertebrate
homology 		HomoloGene:37894  Vertebrate Homology Class
1 human; 1 mouse; 1 rat; 1 chimpanzee; 1 rhesus macaque; 1 cattle; 1 dog; 1 chicken; 1 zebrafish

Protein SuperFamily: ubiquitin thiolesterase
Gene Tree: Uchl1
Human
homologs
Human Homolog UCHL1, ubiquitin carboxyl-terminal esterase L1 (ubiquitin thiolesterase)
NCBI Gene ID 7345
neXtProt AC  NX_P09936
Human Synonyms  PARK5, PGP95, PGP 9.5, PGP9.5, Uch-L1
Human Chr (Location)  4p14; chr4:41258898-41270446 (+)  GRCh37.p10
Disease Associations  (1) Diseases Associated with Human UCHL1
Alleles
and
phenotypes 		All alleles(6) : Targeted(3) Spontaneous(3)
 
Mice homozygous for one allele show ataxia beginning at 80 days of age, followed by progressive tremors, impaired locomotion, atrophy of hind limb muscles, and death by 5-6 months. Mice homozygous for a second allele exhibit defects in motor coordination and decreases in thermal pain sensation.
 
Gene Ontology
(GO)
classifications 		All GO classifications: (36 annotations)
Process adult walking behavior, axonogenesis, ...
Component axon, cytoplasm, ...
Function alpha-2A adrenergic receptor binding, cysteine-type endopeptidase activity, ...
External Resources: FuncBase
Expression Literature Summary: (139 records)
Data Summary: Results (496)    Tissues (275)    Images (109)
Theiler Stages: 9, 13, 15, 17, 19, 20, 22, 23, 25, 26, 28
Assay TypeResults
Immunohistochemistry 106
RNA in situ 291
In situ reporter (knock in) 56
Western blot 2
RT-PCR 41
cDNA source data(12)
External Resources: Allen Institute   GENSAT   GEO   ArrayExpress
Molecular
reagents 		All nucleic(16) cDNA(13) Primer pair(3)
Microarray probesets(3)
Other database
links
VEGA Gene ModelOTTMUSG00000042268 (Evidence)
Ensembl Gene ModelENSMUSG00000029223 (Evidence)
Entrez Gene22223 (Evidence)
DFCITC1573461
DoTSDT.101185072, DT.536408, DT.91284313
NIA Mouse Gene IndexU005644
EC6.-.-.-, 3.4.19.12
Consensus CDS ProjectCCDS19315.1
International Mouse Knockout Project StatusUchl1
Sequences
Representative SequencesLengthStrain/SpeciesFlank
genomic OTTMUSG00000042268 VEGA Gene Model | MGI Sequence Detail 11134 C57BL/6J ±  kb
transcript OTTMUST00000111175 VEGA | MGI Sequence Detail 1167 Not Applicable 
polypeptide OTTMUSP00000062165 VEGA | MGI Sequence Detail 223 Not Applicable 

For the selected sequences
All sequences(38) RefSeq(2) UniProt(3)
Polymorphisms SNPs(63 from dbSNP Build 128)
Protein-related
information
ResourceIDDescription
InterPro IPR001578 Peptidase C12, ubiquitin carboxyl-terminal hydrolase 1
Protein Ontology PR:000017024 ubiquitin carboxyl-terminal hydrolase isozyme L1
References (Earliest) J:14916 Yamazaki K, et al., Location of gracile axonal dystrophy (gad) on Chromosome 5 of the mouse. Jpn J Genet. 1987;62:479-84
(Latest) J:190636 Wiese CB, et al., A genome-wide screen to identify transcription factors expressed in pelvic Ganglia of the lower urinary tract. Front Neurosci. 2012;6:130
All references(213)
Other
accession IDs 		MGD-MRK-24015, MGD-MRK-9952, MGI:2141250, MGI:2141346, MGI:2141354, MGI:95631
Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
Citing These Resources
Funding Information
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Send questions and comments to User Support. 		last database update
05/08/2013
MGI 5.13 		The Jackson Laboratory