frmd4a Phenotypes

Phenotypes

XB-GENEPAGE-5922924

Gene Symbol: frmd4a Gene Name: FERM domain containing 4A

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: frmd4a assayed (1 source)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (34 sources): Absent speech, Agenesis of corpus callosum, Anteverted nares, Aplasia/Hypoplasia of the corpus callosum, Ataxia, Cerebellar hypoplasia, Cerebellar vermis hypoplasia, Everted lower lip vermilion, Global developmental delay, Growth delay, Highly arched eyebrow, Hirsutism, Intellectual disability, Intellectual disability, severe, Limb hypertonia, Long eyelashes, Low anterior hairline, Low-set ears, Low-set, posteriorly rotated ears, Microcephaly, Narrow forehead, Nonprogressive cerebellar ataxia, Palpebral edema, Partial agenesis of the corpus callosum, Poor speech, Posteriorly rotated ears, Primary microcephaly, Protruding ear, Sparse hair, Spasticity, Strabismus, Thick eyebrow, Thick lower lip vermilion, Upper eyelid edema [+]
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): Absent speech, Agenesis of corpus callosum, Anteverted nares, Aplasia/Hypoplasia of the corpus callosum, Ataxia, Cerebellar hypoplasia, Cerebellar vermis hypoplasia, Everted lower lip vermilion, Global developmental delay, Growth delay, [+]