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Expression profile for YHR037W (YHR037W)

Description : Delta-1-pyrroline-5-carboxylate dehydrogenase; nuclear-encoded mitochondrial protein involved in utilization of proline as sole nitrogen source; deficiency of human homolog ALDH4A1 causes type II hyperprolinemia (HPII), an autosomal recessive inborn error of metabolism; human homolog ALDH4A1 can complement yeast null mutant [Source:SGD;Acc:S000001079]

Sample enrichment: YEP + lactic acid,WT (SPM: 0.31, entropy: 3.69, tau: 0.62)
Perturbation specificity: YEP (SPM: 0.49, entropy: 3.25, tau: 0.51)

All conditions


Perturbation specificity

Note: SPM calculations for this profile are done using the maximum value.