Zinc Finger Protein 674 (ZNF674)

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ZNF673B; MRX92

Zinc Finger Protein 674 (ZNF674)
ZNF674 encodes a zinc finger protein with an N-terminal Kruppel-associated box-containing (KRAB) domain and 11 Kruppel-type C2H2 zinc finger domains. Like other zinc finger proteins, this gene may function as a transcription factor. This gene resides on an area of chromosome X that has been implicated in nonsyndromic X-linked mental retardation. Alternative splicing results in multiple transcript variants encoding different isoforms.The ZNF674 cDNA encodes a protein with KRAB A and B domains and 11 Kruppel-type C2H2 zinc finger domains. The transcript of ZNF674 has an open reading frame of 1,743 basepairs, with start and stop codons at positions 212 and 1955 of the cDNA, respectively. PCR of cDNA showed expression of ZNF674 in fetal brain, Epstein-Barr virus-immortalized B lymphocyte cell lines (EBV-LCLs), and testis.

Organism species: Homo sapiens (Human)

CATALOG NO. PRODUCT NAME APPLICATIONS
Proteins n/a Recombinant Zinc Finger Protein 674 (ZNF674) Recombinant Protein Customized Service Offer
Antibodies n/a Monoclonal Antibody to Zinc Finger Protein 674 (ZNF674) Monoclonal Antibody Customized Service Offer
n/a Polyclonal Antibody to Zinc Finger Protein 674 (ZNF674) Polyclonal Antibody Customized Service Offer
Assay Kits n/a CLIA Kit for Zinc Finger Protein 674 (ZNF674) CLIA Kit Customized Service Offer
n/a ELISA Kit for Zinc Finger Protein 674 (ZNF674) ELISA Kit Customized Service Offer
  1. "ZNF674: a new Kruppel-associated box-containing zinc-finger gene involved in nonsyndromic X-linked mental retardation."Am. J. Hum. Genet. 78:265-278(2006) [PubMed] [Europe PMC] [Abstract]
  2. "Complete sequencing and characterization of 21,243 full-length human cDNAs." Nat. Genet. 36:40-45(2004) [PubMed] [Europe PMC] [Abstract]
  3. "The DNA sequence of the human X chromosome." Nature 434:325-337(2005) [PubMed] [Europe PMC] [Abstract]
  4. "XLID-causing mutations and associated genes challenged in light of data from large-scale human exome sequencing."Am. J. Hum. Genet. 93:368-383(2013) [PubMed] [Europe PMC] [Abstract]