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Vectors for Human NBPF7P

Gene Information

  • Offical Gene Symbol NBPF7P
  • Species Human (Homo sapiens)
  • Offical Full Name NBPF member 7, pseudogene
  • Other Aliases NBPF7
  • Other Desigations NBPF member 7; neuroblastoma breakpoint family member 7; putative neuroblastoma breakpoint family member 7
  • Gene Type pseudo
  • Summary
    This gene is a member of the neuroblastoma breakpoint family (NBPF) which consists of dozens of recently duplicated genes primarily located in segmental duplications on human chromosome 1. This gene family has experienced its greatest expansion within the human lineage and has expanded, to a lesser extent, among primates in general. Members of this gene family are characterized by tandemly repeated copies of DUF1220 protein domains. Gene copy number variations in the human chromosomal region 1q21.1, where most DUF1220 domains are located, have been implicated in a number of developmental and neurogenetic diseases such as microcephaly, macrocephaly, autism, schizophrenia, cognitive disability, congenital heart disease, neuroblastoma, and congenital kidney and urinary tract anomalies. Altered expression of some gene family members is associated with several types of cancer. This gene family contains numerous pseudogenes. [provided by RefSeq, Mar 2013]
  • NCBI Gene ID 343505
  • RefSeq Transcript
  • RefSeq Protein
    -; -
  • External Links NCBI  | OMIM  | HGNCUCSC Genome Browser View
No vectors are found in our database for this gene. We may introduce vectors for this gene in the future.

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