mysm1 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (188)

Interactants (4)

XB-GENEPAGE-1032956

Gene Symbol: mysm1 Gene Name: Myb like, SWIRM and MPN domains 1

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (15 sources): Abnormal facial shape, Anemia, Bone marrow hypocellularity, Decreased circulating immunoglobulin concentration, Decreased total leukocyte count, Dry skin, Eczematoid dermatitis, Global developmental delay, Low-set ears, Microcephaly, Midface retrusion, Recurrent respiratory infections, Rhizomelia, Short stature, Thrombocytopenia [+]
Mouse (41 sources): abnormal body length, abnormal bone mineralization, abnormal common lymphocyte progenitor cell morphology, abnormal coping response, abnormal cranium morphology, abnormal hair cycle, abnormal hair follicle morphology, abnormal hindlimb morphology, abnormal tail morphology, abnormal T cell differentiation, abnormal vertebral arch morphology, arrested B cell differentiation, belly spot, curly tail, decreased body length, decreased erythrocyte cell number, decreased hematocrit, decreased hematopoietic cell number, decreased hemoglobin content, decreased immature B cell number, decreased lean body mass, decreased locomotor activity, decreased mature B cell number, decreased pre-B cell number, decreased pro-B cell number, decreased sacral vertebrae number, decreased tail pigmentation, decreased thermal nociceptive threshold, distorted hair follicle pattern, increased bone mineral content, increased circulating alkaline phosphatase level, increased foot pad pigmentation, increased granulocyte number, increased heart weight, increased IgG2b level, increased lean body mass, increased mean corpuscular hemoglobin concentration, increased total body fat amount, kinked tail, short tail, trunk curl [+]
View all ortholog results at Monarch