2024年12月24日 · ASIP (Agouti Signaling Protein) is a Protein Coding gene. Diseases associated with ASIP include Skin/Hair/Eye Pigmentation, Variation In, 9 and Obesity And Hypopigmentation . Among its related pathways are Adipogenesis and GPR143 in melanocytes and retinal pigment epithelium cells .

2024年12月25日 · Complete information for lnc-ASIP-2 gene (RNA Gene), , including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月25日 · PARD3 (Par-3 Family Cell Polarity Regulator) is a Protein Coding gene. Diseases associated with PARD3 include Neural Tube Defects and Prostate Cancer. Among its related pathways are Cell junction organization and Signaling by TGFB family members.

2024年12月25日 · Complete information for MC4R gene (Protein Coding), Melanocortin 4 Receptor, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

Showing 25 of 461 results for ASIP Search Time: 0 ms in Aliases & Descriptions Drugs & Compounds Disorders Text-Mined Disorders Domains Expression in Human Tissues Function Genomics Localization Orthologs Paralogs Pathways Phenotypes Proteins Publications Summaries Transcripts Variants in category Protein Coding RNA Gene Functional Element ...

2024年12月24日 · AIP (Aryl Hydrocarbon Receptor Interacting Protein) is a Protein Coding gene. Diseases associated with AIP include Pituitary Adenoma 1, Multiple Types and Growth Hormone Secreting Pituitary Adenoma .

2024年12月25日 · Complete information for ENSG00000289720 gene (Protein Coding), Novel Protein, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月24日 · Complete information for DENRP1 gene (Pseudogene), DENR Pseudogene 1, including: function, proteins, disorders, pathways, orthologs, and expression. GeneCards - The Human Gene Compendium

2024年12月24日 · AHCY (Adenosylhomocysteinase) is a Protein Coding gene. Diseases associated with AHCY include Hypermethioninemia With S-Adenosylhomocysteine Hydrolase Deficiency and S-Adenosylhomocysteine Hydrolase Deficiency .

2024年12月25日 · MC2R (Melanocortin 2 Receptor) is a Protein Coding gene. Diseases associated with MC2R include Glucocorticoid Deficiency 1 and Familial Glucocorticoid Deficiency. Among its related pathways are Class A/1 (Rhodopsin-like …