rnf125 Phenotypes

XB-GENEPAGE-6048592

Gene Symbol: rnf125 Gene Name: ring finger protein 125, E3 ubiquitin protein ligase

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: rnf125 assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (36 sources): Anteverted nares, Anxiety, Apnea, Cavum septum pellucidum, Cerebral cortical atrophy, Cerebral palsy, Clumsiness, Delayed cranial suture closure, Delayed speech and language development, Gait disturbance, Gastroesophageal reflux, Generalized hypotonia, Hemihypertrophy, Hydrocephalus, Hypertrichosis, Hypoglycemia, Hypoinsulinemia, Hypotonia, Intellectual disability, Keratoconjunctivitis sicca, Large forehead, Macrocephaly, Macroglossia, Mandibular prognathia, obsolete Psychomotor retardation, Osteopenia, Pneumonia, Raynaud phenomenon, Scoliosis, Seizure, Stomatitis, Syncope, Telecanthus, Thick eyebrow, Ventriculomegaly, Wide nose [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (36 sources): Anteverted nares, Anxiety, Apnea, Cavum septum pellucidum, Cerebral cortical atrophy, Cerebral palsy, Clumsiness, Delayed cranial suture closure, Delayed speech and language development, Gait disturbance, [+]