| Monarch Ortholog Phenotypes
|
Human (39 sources):
Abnormal cartilage morphology,
Abnormality of coagulation,
Abnormality of long bone morphology,
Abnormality of the metaphysis,
Anemia,
Astrocytoma,
Bone pain,
Breast carcinoma,
Cerebral palsy,
Chondrosarcoma,
Cranial nerve paralysis,
Dysphagia,
Exostoses,
Goiter,
Growth delay,
Hemangioma,
Hemangiomatosis,
Joint stiffness,
Lymphangioma,
Micromelia,
Multiple enchondromatosis,
Neoplasm,
Neoplasm of the adrenal cortex,
Neoplasm of the parathyroid gland,
Osteolysis,
Ovarian neoplasm,
Parathyroid adenoma,
Pathologic fracture,
Pituitary adenoma,
Platyspondyly,
Precocious puberty,
Recurrent fractures,
Sarcoma,
Scoliosis,
Short stature,
Skin ulcer,
Subcutaneous nodule,
Venous thrombosis,
Visceral angiomatosis
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Mouse (22 sources):
abnormal blood homeostasis,
abnormal bone marrow cell morphology/development,
abnormal bone marrow cell physiology,
abnormal cartilage development,
abnormal common lymphocyte progenitor cell morphology,
abnormal common myeloid progenitor cell morphology,
abnormal long bone epiphyseal plate morphology,
abnormal myeloblast morphology/development,
abnormal tracheal cartilage morphology,
decreased CD4-positive, alpha beta T cell number,
decreased body size,
decreased bone marrow cell number,
decreased common myeloid progenitor cell number,
decreased hematocrit,
decreased hemoglobin content,
hematopoietic system phenotype,
increased CD4-positive, alpha beta T cell number,
increased erythrocyte cell number,
increased hematopoietic stem cell number,
postnatal lethality, complete penetrance,
prenatal lethality, incomplete penetrance,
preweaning lethality, incomplete penetrance
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View all ortholog results at Monarch
|
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.