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krtt1c19e

Official Full Name
keratin, type 1, 19e
Organism
Danio rerio
GeneID
553371
Background
Predicted to enable structural molecule activity. Predicted to be located in intermediate filament. Predicted to be active in cytoskeleton. Is expressed in cornea; epidermis; and keratinocyte. Human ortholog(s) of this gene implicated in several diseases, including corneal dystrophy (multiple); ectodermal dysplasia (multiple); epidermolytic hyperkeratosis (multiple); focal nonepidermolytic palmoplantar keratoderma 1; and pachyonychia congenita. Orthologous to several human genes including KRT13 (keratin 13); KRT14 (keratin 14); and KRT15 (keratin 15). [provided by Alliance of Genome Resources, Feb 2025]
Synonyms
krtt1c19e; im:6905469; si:dkeyp-113d7.4;

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