ZBTB24 gene

zinc finger and BTB domain containing 24

The information on this page was automatically extracted from online scientific databases.

From NCBI Gene:

This gene encodes a protein similar to a protein in rodents which is induced by bone morphogenic protein 2 in vitro. [provided by RefSeq, Aug 2011]

From UniProt:

May be involved in BMP2-induced transcription.

From NCBI Gene:

  • Immunodeficiency-centromeric instability-facial anomalies syndrome 2

From UniProt:

Immunodeficiency-centromeric instability-facial anomalies syndrome 2 (ICF2): A rare disorder characterized by a variable immunodeficiency resulting in recurrent infections, facial anomalies, and branching of chromosomes 1, 9, and 16. Other variable symptoms include growth retardation, failure to thrive, and psychomotor retardation. Laboratory studies show limited hypomethylation of DNA in a small fraction of the genome in some, but not all, patients. [MIM:614069]

Cytogenetic Location: 6q21, which is the long (q) arm of chromosome 6 at position 21

Molecular Location: base pairs 109,462,516 to 109,483,237 on chromosome 6 (Homo sapiens Annotation Release 108, GRCh38.p7) (NCBI)

Cytogenetic Location: 6q21, which is the long (q) arm of chromosome 6 at position 21
  • BIF1
  • ICF2
  • PATZ2
  • ZNF450