{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,19]],"date-time":"2026-10-19T22:05:52Z","timestamp":1792447552092,"version":"4.5.0"},"reference-count":65,"publisher":"Wiley","issue":"3","license":[{"start":{"date-parts":[[2018,11,6]],"date-time":"2018-11-06T00:00:00Z","timestamp":1541462400000},"content-version":"vor","delay-in-days":0,"URL":"http:\/\/onlinelibrary.wiley.com\/termsAndConditions#vor"}],"funder":[{"DOI":"10.13039\/100000002","name":"National Institutes of Health","doi-asserted-by":"publisher","award":["1ZIAHG000136\u201018"],"award-info":[{"award-number":["1ZIAHG000136\u201018"]}],"id":[{"id":"10.13039\/100000002","id-type":"DOI","asserted-by":"publisher"}]}],"content-domain":{"domain":["onlinelibrary.wiley.com"],"crossmark-restriction":true},"short-container-title":["Pigment Cell Melanoma Res"],"published-print":{"date-parts":[[2019,5]]},"abstract":"<jats:title>Abstract<\/jats:title>\n                  <jats:p>Over the past century, studies of human pigmentary disorders along with mouse and zebrafish models have shed light on the many cellular functions associated with visible pigment phenotypes. This has led to numerous genes annotated with the ontology term \u201cpigmentation\u201d in independent human, mouse, and zebrafish databases. Comparisons among these datasets revealed that each is individually incomplete in documenting all genes involved in integument\u2010based pigmentation phenotypes. Additionally, each database contained inherent species\u2010specific biases in data annotation, and the term \u201cpigmentation\u201d did not solely reflect integument pigmentation phenotypes. This review presents a comprehensive, cross\u2010species list of 650 genes involved in pigmentation phenotypes that was compiled with extensive manual curation of genes annotated in OMIM, MGI, ZFIN, and GO. The resulting cross\u2010species list of genes both intrinsic and extrinsic to integument pigment cells provides a valuable tool that can be used to expand our knowledge of complex, pigmentation\u2010associated pathways.<\/jats:p>","DOI":"10.1111\/pcmr.12743","type":"journal-article","created":{"date-parts":[[2018,10,19]],"date-time":"2018-10-19T10:28:14Z","timestamp":1539944894000},"page":"348-358","update-policy":"https:\/\/doi.org\/10.1002\/crossmark_policy","source":"Crossref","is-referenced-by-count":131,"title":["A curated gene list for expanding the horizons of pigmentation biology"],"prefix":"10.1111","volume":"32","author":[{"ORCID":"https:\/\/orcid.org\/0000-0001-7941-1088","authenticated-orcid":false,"given":"Laura L.","family":"Baxter","sequence":"first","affiliation":[{"name":"Genetic Disease Research Branch National Human Genome Research Institute, National Institutes of Health Bethesda Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Dawn E.","family":"Watkins\u2010Chow","sequence":"additional","affiliation":[{"name":"Genetic Disease Research Branch National Human Genome Research Institute, National Institutes of Health Bethesda Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"William J.","family":"Pavan","sequence":"additional","affiliation":[{"name":"Genetic Disease Research Branch National Human Genome Research Institute, National Institutes of Health Bethesda Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"ORCID":"https:\/\/orcid.org\/0000-0002-1958-4689","authenticated-orcid":false,"given":"Stacie K.","family":"Loftus","sequence":"additional","affiliation":[{"name":"Genetic Disease Research Branch National Human Genome Research Institute, National Institutes of Health Bethesda Maryland"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"311","published-online":{"date-parts":[[2018,11,6]]},"reference":[{"key":"e_1_2_10_2_1","doi-asserted-by":"publisher","DOI":"10.1111\/j.1755-148X.2010.00679.x"},{"key":"e_1_2_10_3_1","doi-asserted-by":"crossref","first-page":"1.2.1\u20131.2.12","DOI":"10.1002\/cpbi.27","article-title":"Searching online mendelian inheritance in man (OMIM): A knowledgebase of human genes and genetic phenotypes","volume":"58","author":"Amberger J. 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