This gene is located in the Prader-Willi syndrome region on chromosome 15. This gene is biallelically expressed in adult testis and brain but is paternally imprinted in fetal brain. Defects in this gene may be associated with Prader-Willi syndrome.
A synthesized peptide derived from human NPAS1, corresponding to a region within the internal amino acids.
A synthesized peptide derived from human NPAS2, corresponding to a region within the internal amino acids.
A synthesized peptide derived from Human NPAT.
Interacts specifically with a number of opioid ligands. Receptor for neuropeptides B and W, which may be involved in neuroendocrine system regulation, food intake and the organization of other signals. Has a higher affinity for neuropeptide B.
A synthesized peptide derived from human NPC1L1, corresponding to a region within N-terminal amino acids.
A synthesized peptide derived from human NPC2, corresponding to a region within N-terminal amino acids.
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