ZFPM2 gene

zinc finger protein, FOG family member 2

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

From NCBI Gene:

The zinc finger protein encoded by this gene is a widely expressed member of the FOG family of transcription factors. The family members modulate the activity of GATA family proteins, which are important regulators of hematopoiesis and cardiogenesis in mammals. It has been demonstrated that the protein can both activate and down-regulate expression of GATA-target genes, suggesting different modulation in different promoter contexts. A related mRNA suggests an alternatively spliced product but this information is not yet fully supported by the sequence. [provided by RefSeq, Jul 2008]

From UniProt:

Transcription regulator that plays a central role in heart morphogenesis and development of coronary vessels from epicardium, by regulating genes that are essential during cardiogenesis. Essential cofactor that acts via the formation of a heterodimer with transcription factors of the GATA family GATA4, GATA5 and GATA6. Such heterodimer can both activate or repress transcriptional activity, depending on the cell and promoter context. Also required in gonadal differentiation, possibly be regulating expression of SRY. Probably acts a corepressor of NR2F2 (By similarity).

Covered on Genetics Home Reference:

From NCBI Gene:

  • Diaphragmatic hernia 3
  • 46,XY sex reversal 9
  • Tetralogy of Fallot

From UniProt:

Tetralogy of Fallot (TOF): A congenital heart anomaly which consists of pulmonary stenosis, ventricular septal defect, dextroposition of the aorta (aorta is on the right side instead of the left) and hypertrophy of the right ventricle. In this condition, blood from both ventricles (oxygen-rich and oxygen-poor) is pumped into the body often causing cyanosis. [MIM:187500]

Diaphragmatic hernia 3 (DIH3): Form of congenital diaphragmatic hernia (CDH). CDH refers to a group of congenital defects in the structural integrity of the diaphragm associated with often lethal pulmonary hypoplasia and pulmonary hypertension. [MIM:610187]

Conotruncal heart malformations (CTHM): A group of congenital heart defects involving the outflow tracts. Examples include truncus arteriosus communis, double-outlet right ventricle and transposition of great arteries. Truncus arteriosus communis is characterized by a single outflow tract instead of a separate aorta and pulmonary artery. In transposition of the great arteries, the aorta arises from the right ventricle and the pulmonary artery from the left ventricle. In double outlet of the right ventricle, both the pulmonary artery and aorta arise from the right ventricle. [MIM:217095]

46,XY sex reversal 9 (SRXY9): A disorder of sex development. Affected individuals have a 46,XY karyotype but present as phenotypically normal females or have ambiguous external genitalia. [MIM:616067]

Cytogenetic Location: 8q23.1, which is the long (q) arm of chromosome 8 at position 23.1

Molecular Location: base pairs 105,318,438 to 105,804,539 on chromosome 8 (Homo sapiens Updated Annotation Release 109.20200522, GRCh38.p13) (NCBI)

Cytogenetic Location: 8q23.1, which is the long (q) arm of chromosome 8 at position 23.1
  • DIH3
  • FOG2
  • hFOG-2
  • SRXY9
  • ZC2HC11B
  • ZNF89B