Metazoan complexes |
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Details of PEPD gene in Homo sapiens
IDs | |||||||||
---|---|---|---|---|---|---|---|---|---|
Link outs | Gene Name | Alias | Uniprot ID | SwissProt ID | NCBI gene ID | ENSEMBL ID | Description | Source | |
| PEPD | PRD | P12955 | PEPD_HUMAN | 5184 | ENSG00000124299 | Xaa-Pro dipeptidase | SPROT |
Disease | |||||||||
---|---|---|---|---|---|---|---|---|---|
Disease | OMIM id | ||||||||
Prolidase deficiency (PD) [MIM:170100]: A multisystem disorder associated with massive iminodipeptiduria and lack of or reduced prolidase activity in erythrocytes, leukocytes, or cultured fibroblasts. Clinical features include skin ulcers, developmental delay, recurrent infections, and a characteristic facies. Note=The disease is caused by mutations affecting the gene represented in this entry. | 170100 |
Orthologs in other species | |||||||||
---|---|---|---|---|---|---|---|---|---|
M. musculus | D. melonogaster | C. elegans | S. purpuratus | ||||||
Pepd | Dip-C | K12C11.1 | Sp-XpapdL |
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
Complex ID | Corum | BioGrid | IRefWeb | Novelty |
---|---|---|---|---|---|---|---|---|---|
Conserved gene 1 |
Conserved gene 2 |
Conserved score |
H. sapiens gene 1 |
H. sapiens gene 2 |
---|---|---|---|---|
LDHB | PEPD | 0.11507798 | LDHB | PEPD |
PEPD | TANGO2 | 0.091099426 | PEPD | TANGO2 |
PEPD | HSPE1 | 0.085643623 | PEPD | HSPE1 |
PEPD | PSMG4 | 0.158385685 | PEPD | PSMG4 |
PEPD | GOT1 | 0.120685505 | PEPD | GOT1 |
RPIA | PEPD | 0.086446246 | RPIA | PEPD |
SOD2 | PEPD | 0.086095877 | SOD2 | PEPD |
LDHA | PEPD | 0.128727202 | LDHA | PEPD |