wbp1l Phenotypes

XB-GENEPAGE-5799642

Gene Symbol: wbp1l Gene Name: WW domain binding protein 1 like

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: wbp1l assayed (6 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (18 sources): abnormal bone marrow cell physiology, abnormal circulating alkaline phosphatase level, abnormal embryonic hematopoiesis, abnormal eye anterior chamber depth, abnormal locomotor activation, abnormal pre-B cell morphology, abnormal retina inner nuclear layer morphology, abnormal skin coloration, decreased B-1 B cell number, decreased circulating alkaline phosphatase level, decreased pre-B cell number, decreased prepulse inhibition, decreased pro-B cell number, immune system phenotype, increased dendritic cell number, increased hematopoietic stem cell number, increased marginal zone B cell number, increased startle reflex [+]

Monarch Ortholog Phenotypes

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

Mouse (18 sources): abnormal bone marrow cell physiology, abnormal circulating alkaline phosphatase level, abnormal embryonic hematopoiesis, abnormal eye anterior chamber depth, abnormal locomotor activation, abnormal pre-B cell morphology, abnormal retina inner nuclear layer morphology, abnormal skin coloration, decreased B-1 B cell number, decreased circulating alkaline phosphatase level, [+]