prdm14 Phenotypes

Phenotypes

XB-GENEPAGE-954694

Gene Symbol: prdm14 Gene Name: PR domain 14

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: prdm14 assayed (27 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (34 sources): abnormal adipose tissue amount, abnormal bone mineralization, abnormal common lymphocyte progenitor cell morphology, abnormal eye posterior chamber depth, abnormal grip strength, abnormal lean body mass, abnormal locomotor activation, abnormal primordial germ cell morphology, abnormal thymus physiology, absent germ cells, arrested B cell differentiation, decreased bone mineral content, decreased double-positive T cell number, decreased grip strength, decreased heart rate variability, decreased lean body mass, decreased locomotor activity, decreased mature B cell number, decreased pre-B cell number, decreased primordial germ cell number, decreased pro-B cell number, decreased thigmotaxis, enlarged lymph nodes, enlarged thymus, immune system phenotype, increased CD8-positive, alpha-beta T cell number, increased acute lymphoblastic leukemia incidence, increased hematopoietic stem cell number, increased large unstained cell number, increased single-positive T cell number, increased total body fat amount, intermingled spleen red and white pulp, meningitis, premature death [+]

Monarch Ortholog Phenotypes

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

Mouse (34 sources): abnormal adipose tissue amount, abnormal bone mineralization, abnormal common lymphocyte progenitor cell morphology, abnormal eye posterior chamber depth, abnormal grip strength, abnormal lean body mass, abnormal locomotor activation, abnormal primordial germ cell morphology, abnormal thymus physiology, absent germ cells, [+]