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Proteintech
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Immunogen sequence: LAKWRCFFH QMAVEQGQAG LAAMDTKLEV AVLQESVAKL GIASRAEIED WFTAETLGVS GTMDLLDWSS LIDSRTKLSK HLVVPNAQTG QLEPLLSRFT EEEELQMTRM LQRMDVLAKK ATEMGVRLMV DAEQTYFQPA ISRLTLEMQR KFNVEKPLIF NTYQCYLKDA YDNVTLDVEL ARREGWCFGA KLVRGAYLAQ ERARAAEIGY EDPINPTYEA TNAMYHRCLD YVLEELKHNA KAKVMVASHN EDTVRFALRR MEELGLHPAD HRVYFGQLLG MCDQISFPLG QAGYPVYKYV PYGPVMEVLP YLSRRALENS SLMKGTHRER QLLWLELLRR LRTGNLFHRP A (143-492 aa encoded by BC118597)
The protein encoded by this gene is a mitochondrial proline dehydrogenase that catalyzes the first step in proline degradation. Defects in this gene are a cause of hyperprolinemia type 1 and possibly susceptibility to schizophrenia 4 (SCZD4). The gene is located on chromosome 22q11.21, a region which has also been associated with the contiguous gene deletion syndromes DiGeorge syndrome and CATCH22 syndrome.
仅用于科研。不用于诊断过程。未经明确授权不得转售。
蛋白别名: p53-induced gene 6 protein; PRODH 1; PRODH 2; proline dehydrogenase (oxidase) 1; proline dehydrogenase (proline oxidase); Proline dehydrogenase 1, mitochondrial; proline dehydrogenase, mitochondrial; Proline oxidase; Proline oxidase 2; proline oxidase, mitochondrial; SCZD4; tumor protein p53 inducible protein 6
基因别名: HSPOX2; PIG6; POX; POX2; Pro-1; Pro1; PRODH; PRODH1; PRODH2; TP53I6; Ym24d07
UniProt ID: (Human) O43272, (Mouse) Q9WU79
Entrez Gene ID: (Human) 5625, (Mouse) 19125, (Rat) 680409