tmem165 Phenotypes

XB-GENEPAGE-972193

Gene Symbol: tmem165 Gene Name: transmembrane protein 165

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: tmem165 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (26 sources): Abnormal cerebral white matter morphology, Amelogenesis imperfecta, Diaphyseal dysplasia, Elevated circulating creatine kinase concentration, Elevated circulating hepatic transaminase concentration, Epiphyseal dysplasia, Failure to thrive, Generalized hypotonia, Global developmental delay, Growth delay, Hepatomegaly, Hypotonia, Kyphoscoliosis, Low-set ears, Malar flattening, Metaphyseal dysplasia, Midface retrusion, Muscle weakness, Osteoporosis, Posteriorly rotated ears, Secondary microcephaly, Seizure, Short stature, Thrombocytopenia, Unexplained fevers, obsolete Joint laxity [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (26 sources): Abnormal cerebral white matter morphology, Amelogenesis imperfecta, Diaphyseal dysplasia, Elevated circulating creatine kinase concentration, Elevated circulating hepatic transaminase concentration, Epiphyseal dysplasia, Failure to thrive, Generalized hypotonia, Global developmental delay, Growth delay, [+]