XB-GENEPAGE-5995329
diaph1 diaphanous related formin 1
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.
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| Computed annotations: diaph1 assayed (1 source) |
| Monarch Ortholog Phenotypes
These phenotypes are associated with this gene with a has phenotype relation via Monarch.
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| Human (15 sources): Cerebral visual impairment, Eczematoid dermatitis, Generalized hypotonia, Growth delay, Hypoplasia of the corpus callosum, Hypotonia, Low-frequency hearing loss, Microcephaly, Optic atrophy, Poor speech, [+] |
| Mouse (30 sources): abnormal bone marrow cell morphology/development, abnormal CD4-positive, alpha beta T cell number, abnormal CD8-positive, alpha-beta T cell number, abnormal definitive hematopoiesis, abnormal humoral immune response, abnormal leukocyte migration, abnormal skin condition, abnormal spleen germinal center morphology, absent spleen white pulp, decreased B-1 B cell number, [+] |
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View all ortholog results at Monarch |