PHD finger protein 6 (PHF6) (NM_032458) Human Tagged ORF Clone Lentiviral Particle

CAT#: RC223100L2V

Lenti ORF particles, PHF6 (mGFP-tagged) - Human PHD finger protein 6 (PHF6), transcript variant 2, 200ul, >10^7 TU/mL

Specifications

Product Data

• Type: Human Tagged ORF Clone Lentiviral Particle
• Tag: mGFP
• Symbol: PHD finger protein 6
• Synonyms: BFLS; BORJ; CENP-31
• Mammalian Cell Selection: None
• Vector: pLenti-C-mGFP
• ACCN: NM_032458
• ORF Size: 1095 bp
• Sequence Data:
  ORF Nucleotide Sequence

  The ORF insert of this clone is exactly the same as(RC223100).
• OTI Disclaimer: The molecular sequence of this clone aligns with the gene accession number as a point of reference only. However, individual transcript sequences of the same gene can differ through naturally occurring variations (e.g. polymorphisms), each with its own valid existence. This clone is substantially in agreement with the reference, but a complete review of all prevailing variants is recommended prior to use. More info
• OTI Annotation: This clone was engineered to express the complete ORF with an expression tag. Expression varies depending on the nature of the gene.

Reference Data

• RefSeq: NM_032458.2
• RefSeq Size: 4772 bp
• RefSeq ORF: 1098 bp
• Locus ID: 84295
• UniProt ID: Q8IWS0
• Cytogenetics: Xq26.2
• Protein Families: Druggable Genome, Transcription Factors
• MW: 41.1 kDa
• Gene Summary: This gene is a member of the plant homeodomain (PHD)-like finger (PHF) family. It encodes a protein with two PHD-type zinc finger domains, indicating a potential role in transcriptional regulation, that localizes to the nucleolus. Mutations affecting the coding region of this gene or the splicing of the transcript have been associated with Borjeson-Forssman-Lehmann syndrome (BFLS), a disorder characterized by cognitive disability, epilepsy, hypogonadism, hypometabolism, obesity, swelling of subcutaneous tissue of the face, narrow palpebral fissures, and large ears. Alternate splicing results in multiple transcript variants, encoding different isoforms. [provided by RefSeq, Jun 2010]