zfpm1 Phenotypes

Phenotypes

XB-GENEPAGE-940293

Gene Symbol: zfpm1 Gene Name: zinc finger protein, FOG family member 1

Expression Phenotypes Gene expression phenotype annotations where the gene of interest has been disrupted (manipulated) or is the gene assayed (assayed). Computed annotations are derived from differential expression analysis from Xenbase processed GEO data with the criteria of a TPM >= 1, FDR <= 0.05 and an absolute LogFC >= 2.
Computed annotations: zfpm1 assayed (2 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (36 sources): abnormal bone marrow cell number, abnormal circulating chemokine level, abnormal common myeloid progenitor cell morphology, abnormal embryonic erythropoiesis, abnormal erythropoiesis, abnormal megakaryocyte differentiation, abnormal megakaryocyte morphology, abnormal megakaryocyte progenitor cell morphology, abnormal vitelline vasculature morphology, atrioventricular septal defect, cardiovascular system phenotype, common atrioventricular valve, decreased embryo size, decreased platelet alpha-granule number, decreased spleen white pulp amount, embryonic lethality during organogenesis, complete penetrance, embryonic lethality during organogenesis, incomplete penetrance, hematopoietic system phenotype, impaired hematopoiesis, increased erythrocyte cell number, increased granulocyte number, increased heart weight, increased hemoglobin concentration distribution width, increased neutrophil cell number, increased red blood cell distribution width, increased spleen red pulp amount, increased spleen weight, lethality throughout fetal growth and development, complete penetrance, lethality throughout fetal growth and development, incomplete penetrance, no abnormal phenotype detected, pale liver, pale yolk sac, pericardial edema, perinatal lethality, incomplete penetrance, small liver, thin myocardium [+]

Monarch Ortholog Phenotypes

These phenotypes are associated with this gene with a has phenotype relation via Monarch.

Mouse (36 sources): abnormal bone marrow cell number, abnormal circulating chemokine level, abnormal common myeloid progenitor cell morphology, abnormal embryonic erythropoiesis, abnormal erythropoiesis, abnormal megakaryocyte differentiation, abnormal megakaryocyte morphology, abnormal megakaryocyte progenitor cell morphology, abnormal vitelline vasculature morphology, atrioventricular septal defect, [+]