NEGR1 | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Aliases | NEGR1 , DMML2433, IGLON4, KILON, Ntra, neuronal growth regulator 1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
External IDs | OMIM: 613173 MGI: 2444846 HomoloGene: 41447 GeneCards: NEGR1 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Wikidata | |||||||||||||||||||||||||||||||||||||||||||||||||||
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Neuronal growth regulator 1 also known as NEGR1 is a protein which in humans is encoded by the NEGR1 gene. [5]
Variants of the NEGR1 gene may be associated with obesity and major depression. [6] [7] [8]
Collagen alpha-1 (XXVII) chain (COL27A1) is a protein that in humans is encoded by the COL27A1 gene.
Apolipoprotein C-IV, also known as apolipoprotein C4, is a protein that in humans is encoded by the APOC4 gene.
Sialomucin core protein 24 also known as endolyn or CD164 is a protein that in humans is encoded by the CD164 gene. CD164 functions as a cell adhesion molecule.
Melanocortin 4 receptor (MC4R) is a melanocortin receptor that in humans is encoded by the MC4R gene. It encodes the MC4R protein, a G protein-coupled receptor (GPCR) that binds α-melanocyte stimulating hormone (α-MSH). In mouse models, MC4 receptors have been found to be involved in feeding behaviour, the regulation of metabolism, sexual behaviour, and male erectile function.
McKusick–Kaufman/Bardet–Biedl syndromes putative chaperonin is a protein that in humans is encoded by the MKKS gene.
Bardet–Biedl syndrome 1 protein is a protein that in humans is encoded by the BBS1 gene. BBS1 is part of the BBSome complex, which required for ciliogenesis. Mutations in this gene have been observed in patients with the major form of Bardet–Biedl syndrome.
Proline/serine-rich coiled-coil protein 1 is a protein that in humans is encoded by the PSRC1 gene.
Ventral anterior homeobox 1 is a protein that in humans is encoded by the VAX1 gene.
Dipeptidase 3 (DPEP3) is a protein that in humans is encoded by the DPEP3 gene.
Dystrobrevin beta is a protein which in humans is encoded by the DTNB gene.
Transmembrane protein 18 also known as TMEM18 is a protein which in humans is encoded by the TMEM18 gene.
Glucosamine-6-phosphate deaminase 2 also known as GNPDA2 is an enzyme that in humans is encoded by the GNPDA2 gene.
Potassium channel tetramerisation domain containing 15 also known as BTB/POZ domain-containing protein KCTD15 is protein that in humans is encoded by the KCTD15 gene.
Like many other medical conditions, obesity is the result of an interplay between environmental and genetic factors. Studies have identified variants in several genes that may contribute to weight gain and body fat distribution; although, only in a few cases are genes the primary cause of obesity.
Centrosomal protein of 120 kDa (Cep120), also known as coiled-coil domain-containing protein 100, is a protein that in humans is encoded by the CEP120 gene.
Popeye domain-containing protein 3 is a protein that in humans is encoded by the POPDC3 gene.
Zinc finger protein 57 homolog (ZFP57), also known as zinc finger protein 698 (ZNF698), is a protein that in humans is encoded by the ZFP57 gene.
WD repeat-containing protein 72 is a protein that in humans is encoded by the WDR72 gene. WDR72 contains 7 WD40 repeats, which are predicted to form the blades of a 7 beta propeller structure.
Interferon kappa, also known as IFN-kappa, is a protein that in humans is encoded by the IFNK gene.
Monocarboxylate transporter 9 is a protein that in humans is encoded by the SLC16A9 gene.