Prolactin regulatory element-binding protein is a
protein that in humans is encoded by the PREBgene.[5][6][7]
This gene encodes a protein that specifically binds to a Pit1-binding element of the prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand.[7]
Taylor Clelland CL, Levy B, McKie JM, et al. (2000). "Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome". Mamm. Genome. 11 (8): 675–681.
doi:
10.1007/s003350010142.
PMID10920239.
S2CID22946856.
Prolactin regulatory element-binding protein is a
protein that in humans is encoded by the PREBgene.[5][6][7]
This gene encodes a protein that specifically binds to a Pit1-binding element of the prolactin (PRL) promoter. This protein may act as a transcriptional regulator and is thought to be involved in some of the developmental abnormalities observed in patients with partial trisomy 2p. This gene overlaps the abhydrolase domain containing 1 (ABHD1) gene on the opposite strand.[7]
Taylor Clelland CL, Levy B, McKie JM, et al. (2000). "Cloning and characterization of human PREB; a gene that maps to a genomic region associated with trisomy 2p syndrome". Mamm. Genome. 11 (8): 675–681.
doi:
10.1007/s003350010142.
PMID10920239.
S2CID22946856.