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Proteintech
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Immunogen sequence: RRWKRNWFA LWLDGTLGYY HDETAQDEED RVLIHFNVRD IKIGPECHDV QPPEGRSRDG LLTVNLREGG RLHLCAETKD DALAWKTALL EANSTPVRVY SPYQDYYEVV PPNAHEATYV RSYYGPPYAG PGVTHVIVRE DPCYSAGAPL AMGMLAGAAT GAALGSLMWS PCWF (17-189 aa encoded by BC008075)
PHR1 is a transcription factor known to participate in the regulation of genes involved in phosphate homeostasis and the regulation of genes involved in inter organ sulfate transport. Diseases associated with PHR1 protein mutation include Wallerian Degeneration and deafness due to Autosomal Recessive 63 dysfunction.
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: Evectin-1; PH domain containing protein in retina 1; PH domain containing, retinal 1; PH domain-containing family B member 1; PH domain-containing protein in retina 1; PHRET1; pleckstrin homology domain containing, family B (evectins) member 1; Pleckstrin homology domain retinal protein 1; Pleckstrin homology domain-containing family B member 1; retinal 1
基因别名: AI315628; evt-1; EVT1; KPL1; PHR1; PHRET1; PLEKHB1
UniProt ID: (Human) Q9UF11, (Mouse) Q9QYE9, (Rat) Q9WU68
Entrez Gene ID: (Human) 58473, (Mouse) 27276, (Rat) 64471