abcg2 Phenotypes

Phenotypes

XB-GENEPAGE-991894

Gene Symbol: abcg2 Gene Name: ATP binding cassette subfamily G member 2 (Junior blood group)

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: abcg2 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Mouse (22 sources): abnormal bile color, abnormal blood urea nitrogen level, abnormal bone marrow cell morphology/development, abnormal endoplasmic reticulum morphology, abnormal hematopoietic system morphology/development, abnormal hepatocyte morphology, abnormal mitochondrial crista morphology, abnormal mitochondrial physiology, abnormal oxidative phosphorylation, abnormal respiratory electron transport chain, decreased blood urea nitrogen level, decreased liver glycogen level, fused cornea and lens, hematopoietic system phenotype, homeostasis/metabolism phenotype, increased physiological sensitivity to xenobiotic, increased porphyrin level, increased prepulse inhibition, no abnormal phenotype detected, oxidative stress, phototoxicity, porphyria [+]

Monarch Ortholog Phenotypes

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

Mouse (22 sources): abnormal bile color, abnormal blood urea nitrogen level, abnormal bone marrow cell morphology/development, abnormal endoplasmic reticulum morphology, abnormal hematopoietic system morphology/development, abnormal hepatocyte morphology, abnormal mitochondrial crista morphology, abnormal mitochondrial physiology, abnormal oxidative phosphorylation, abnormal respiratory electron transport chain, [+]