rab11b.2 Phenotypes

XB-GENEPAGE-5963249

Gene Symbol: rab11b.2 Gene Name: RAB11B, member RAS oncogene family, gene 2

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: rab11b.2 assayed (3 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (34 sources): Abnormal facial shape, Abnormal pinna morphology, Absent speech, Cerebellar vermis hypoplasia, Clinodactyly, Delayed ability to walk, Delayed myelination, Difficulty walking, Dystonia, Facial hypotonia, Feeding difficulties, Gait ataxia, Generalized hypotonia, Global developmental delay, Happy demeanor, Hip dysplasia, Hypermetropia, Microcephaly, Motor stereotypy, Nystagmus, Optic atrophy, Overlapping toe, Pes cavus, Poor eye contact, Seizure, Single transverse palmar crease, Spasticity, Strabismus, Talipes equinovarus, Tapered finger, Tented upper lip vermilion, Unsteady gait, Upslanted palpebral fissure, Visual impairment [+]
View all ortholog results at Monarch

Monarch Ortholog Phenotypes

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

Human (34 sources): Abnormal facial shape, Abnormal pinna morphology, Absent speech, Cerebellar vermis hypoplasia, Clinodactyly, Delayed ability to walk, Delayed myelination, Difficulty walking, Dystonia, Facial hypotonia, [+]