| Monarch Ortholog Phenotypes
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Human (4 sources):
Abnormality of metabolism/homeostasis,
Intellectual disability,
Strabismus,
Tremor
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Mouse (25 sources):
abnormal coat appearance,
abnormal long bone epiphyseal plate proliferative zone,
abnormal long bone hypertrophic chondrocyte zone,
abnormal ovarian folliculogenesis,
abnormal postnatal growth/weight/body size,
abnormal reproductive system development,
abnormal skeleton development,
absent corpus luteum,
decreased body size,
decreased bone mass,
decreased circulating cysteine level,
decreased glutathione level,
decreased locomotor activity,
decreased long bone epiphyseal plate size,
decreased spleen red pulp amount,
decreased thyroxine level,
diluted coat color,
disproportionate dwarf,
glutathionuria,
hindlimb paralysis,
increased circulating glutathione level,
increased osteoclast cell number,
nervous,
premature death,
skeleton phenotype
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View all ortholog results at Monarch
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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.