fgl1a Phenotypes

Phenotypes

XB-GENEPAGE-979408

Gene Symbol: fgl1a Gene Name: fibrinogen like 1A

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: fgl1a assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (21 sources): abnormal bone mineralization, abnormal brown fat cell morphology, abnormal gluconeogenesis, abnormal liver weight, behavior/neurological phenotype, decreased circulating free fatty acids level, decreased respiratory quotient, decreased tumor growth/size, decreased white fat cell number, dermatitis, growth/size/body region phenotype, homeostasis/metabolism phenotype, increased anti-double stranded DNA antibody level, increased body length, increased brown fat cell lipid droplet size, increased central memory CD8 positive, alpha-beta T cell number, increased liver triglyceride level, increased total body fat amount, increased white adipose tissue amount, increased white fat cell size, macrovesicular hepatic steatosis [+]

Monarch Ortholog Phenotypes

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

Mouse (21 sources): abnormal bone mineralization, abnormal brown fat cell morphology, abnormal gluconeogenesis, abnormal liver weight, behavior/neurological phenotype, decreased circulating free fatty acids level, decreased respiratory quotient, decreased tumor growth/size, decreased white fat cell number, dermatitis, [+]