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Gene : OPLAH Homo sapiens

Name  ? 5-oxoprolinase, ATP-hydrolysing Cytological Location  8q24.3
Brief Description  5-oxoprolinase, ATP-hydrolysing
description  The protein encoded by this gene acts as a homodimer, using ATP hydrolysis to catalyze the conversion of 5-oxo-L-proline to L-glutamate. Defects in this gene are a cause of 5-oxoprolinase deficiency (OPLAHD). [provided by RefSeq, Jun 2012]
  • synonyms:
  • uc033cce.2,
  • OPLAHD,
  • NM_017570,
  • HGNC:8149,
  • 5-Opase,
  • OPLA,
  • OTTHUMG00000165435,
  • AB122018,
  • AF024672,
  • OPLA,
  • 5-Opase,
  • OPLAH
  • identifiers:
  • 26873,
  • ENSG00000178814,
  • OPLAH

Genome feature

Region: gene ? Length: 12761  
Location: 8:144051266-144064026 reverse strand Cyto location: 8q24.3


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Function

Gene Ontology Displayer

Gene --> GO terms.

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Genomics

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Gene --> Chromosomal location.

Gene --> GO terms.

Gene --> Overlapping genes.

Proteins

Gene --> Proteins.

SNPs

Gene Report --> GWAS hit

Disease

1 Diseases

Gene (Hum OR Rat) --> Mouse Allele (Phenotype)

Gene --> Alleles and Disease (clinVar data)

Gene -> HPO annotation (Human Phenotype Ontology)

Mouse Gene --> Allele [Phenotype]

Homology

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Gene --> Orthologues

Interactions

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Gene --> Physical and Genetic Interactions

Expression

Gene(s) --> Significant SNPs (GTex data)

Gene Ontology

Gene --> GO terms.

 

Other

154 SN Ps

5 Cross References

18 Data Sets

6 Homologues

0 Located Features

90 Rna Seq Results