Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
This target displays homology in the following species: Cow: 100%; Dog: 100%; Guinea Pig: 100%; Horse: 93%; Human: 100%; Mouse: 100%; Rabbit: 100%; Rat: 100%
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.
For Research Use Only. Not for use in diagnostic procedures. Not for resale without express authorization.
Protein Aliases: 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
Gene Aliases: EVT1; KPL1; PHR1; PHRET1; PLEKHB1
UniProt ID: (Human) Q9UF11
Entrez Gene ID: (Human) 58473
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