$VAR1 = undef;

Summary for peptidase C19.015: ubiquitin-specific peptidase 14

Summary Gene structure Alignment Tree Sequences Sequence features Distribution Structure Literature

 

Names
MEROPS Nameubiquitin-specific peptidase 14
Other namesTGT subunit, tRNA-guanine transglycosylase 60-kDa subunit, USP14 g.p. (Homo sapiens), USP14, ubiquitin-specific protease 14
Domain architecture
MEROPS Classification
Classification Clan CA >> Subclan (none) >> Family C19 >> Subfamily (none) >> C19.015
Holotypeubiquitin-specific peptidase 14 (Homo sapiens), Uniprot accession P54578 (peptidase unit: 73-494), MERNUM MER0002667
History Identifier created: MEROPS 3.1 (22 December 1998)
Activity
Catalytic typeCysteine
NC-IUBMBNot yet included in IUBMB recommendations.
Activity statushuman: active (Wilson et al., 2002)
mouse: putative
PhysiologyThere is evidence that ubiquitin-specific peptidase 14 functions to maintain the levels of monomeric ubiquitin in mammalian cells (Anderson et al., 2005).
KnockoutMutation in mice is reported to account for hereditary ataxia (Wilson et al., 2002). The ataxia (ax(J)) mutation is a spontaneous recessive mutation that results in reduced expression of ubiquitin-specific protease 14. Mice homozygous for the ax(J) mutation are retarded in growth and exhibit several behavioral disorders, including a resting tremor and hindlimb paralysis (Anderson et al., 2005).
Other databases TREEFAMhttp://www.treefam.org/family/TF314494
Human genetics
Gene symbol Locus Megabases Ensembl Entrez gene Gene Cards OMIM
USP14 18p11.32 ENSG00000101557 9097 USP14 607274
Mouse genetics
Gene symbol Position Megabases Ensembl Entrez gene MGI
Usp14 18:A1 ENSMUSG00000024288 59025 MGI:1928898