$VAR1 = undef;
Summary for peptidase C19.015: ubiquitin-specific peptidase 14
| Names | |
|---|---|
| MEROPS Name | ubiquitin-specific peptidase 14 |
| Other names | TGT 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 |
| Holotype | ubiquitin-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 type | Cysteine | ||
| NC-IUBMB | Not yet included in IUBMB recommendations. | ||
| Activity status | human: active (Wilson et al., 2002) mouse: putative | ||
| Physiology | There is evidence that ubiquitin-specific peptidase 14 functions to maintain the levels of monomeric ubiquitin in mammalian cells (Anderson et al., 2005). | ||
| Knockout | Mutation 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 | TREEFAM | http://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 | ||
