Phenotype profiles of nonsyndromic genes linked to bleeding in combination with platelet dysfunction in mouse. Syndromic genes from supplemental File 1 were filtered for bleeding plus platelet dysfunction in mouse. Indicated in blue type are orthologous human genes from the reference list (known link to hemostasis). Phenotype scoring for humans (h) and mice (m) included the following: 1, bleeding; 2, thrombophilia/arterial thrombosis tendency; 3, platelet function; 4, platelet morphology and development; 5, platelet count; 6, coagulation dysfunction; 7, erythrocyte characteristics; 8, platelet traits from human GWAS (supplemental Figure 1). Indicated are also mean levels of platelet and megakaryocyte transcripts and platelet protein copy numbers. Extended phenotype descriptions per gene are given in supplemental File 1. Coagul, coagulation; MGK, megakaryocyte; P-count, platelet count; P-morph, platelet morphology; P-mRNA, platelet mRNA.