Name

LOC7795 Gene

Methylation modifier for class I HLA

LOC390956 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC101927654 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC105374327 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC100996503 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC105371242 Gene

peptidyl-prolyl cis-trans isomerase A-like 4G

Predicted to enable cyclosporin A binding activity and peptidyl-prolyl cis-trans isomerase activity. Predicted to be involved in protein folding. Predicted to be active in cytoplasm. [provided by Alliance of Genome Resources, Mar 2025]

PTRH2 Gene

peptidyl-tRNA hydrolase 2

The protein encoded by this gene is a mitochondrial protein with two putative domains, an N-terminal mitochondrial localization sequence, and a UPF0099 domain. In vitro assays suggest that this protein possesses peptidyl-tRNA hydrolase activity, to release the peptidyl moiety from tRNA, thereby preventing the accumulation of dissociated peptidyl-tRNA that could reduce the efficiency of translation. This protein also plays a role regulating cell survival and death. It promotes survival as part of an integrin-signaling pathway for cells attached to the extracellular matrix (ECM), but also promotes apoptosis in cells that have lost their attachment to the ECM, a process called anoikos. After loss of cell attachment to the ECM, this protein is phosphorylated, is released from the mitochondria into the cytosol, and promotes caspase-independent apoptosis through interactions with transcriptional regulators. This gene has been implicated in the development and progression of tumors, and mutations in this gene have been associated with an infantile multisystem neurologic, endocrine, and pancreatic disease (INMEPD) characterized by intellectual disability, postnatal microcephaly, progressive cerebellar atrophy, hearing impairment, polyneuropathy, failure to thrive, and organ fibrosis with exocrine pancreas insufficiency (PMID: 25574476). Alternative splicing results in multiple transcript variants encoding different isoforms. [provided by RefSeq, Mar 2015]

PTRH1 Gene

peptidyl-tRNA hydrolase 1 homolog (S. cerevisiae)

Enables aminoacyl-tRNA hydrolase activity. Involved in rescue of stalled ribosome. Located in mitochondrion. [provided by Alliance of Genome Resources, Mar 2025]

LOC101060458 Gene

peptidyl-prolyl cis-trans isomerase A-like

LOC101928610 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC105374236 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC101928624 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC100287361 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC105369232 Gene

peptidyl-prolyl cis-trans isomerase FKBP4 pseudogene

LOC101060363 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC101926910 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC442744 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC105378561 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

ACE3P Gene

angiotensin I converting enzyme (peptidyl-dipeptidase A) 3, pseudogene

Predicted to be located in acrosomal vesicle. [provided by Alliance of Genome Resources, Mar 2025]

LOC100996727 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

PTRHD1 Gene

peptidyl-tRNA hydrolase domain containing 1

This gene encodes the enzyme peptidyl-tRNA hydrolase. Peptidyl-tRNA hydrolases perform the essential function of recycling peptidyl-tRNAs. Mutations in this gene are associated with autosomal-recessive intellectual disability and parkinsonism. [provided by RefSeq, May 2017]

LOC101927689 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene

LOC101928064 Gene

peptidyl-prolyl cis-trans isomerase A pseudogene