fam161a Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (95)

Interactants (142)

XB-GENEPAGE-5821021

Gene Symbol: fam161a Gene Name: FAM161A, centrosomal protein

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (32 sources): Abnormal electroretinogram, Abnormal retinal vascular morphology, Abnormal testis morphology, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Anteverted nares, Atypical scarring of skin, Blindness, Bone spicule pigmentation of the retina, Cataract, Conductive hearing impairment, Constriction of peripheral visual field, Glaucoma, Hyperinsulinemia, Hyperreflexia, Hypogonadism, Hypoplasia of penis, Intellectual disability, Keratoconus, Nyctalopia, Nystagmus, Obesity, Ophthalmoplegia, Optic atrophy, Optic disc pallor, Photophobia, Progressive night blindness, Rod-cone dystrophy, Sensorineural hearing impairment, Type II diabetes mellitus, Visual impairment, Wide nasal bridge [+]
Mouse (29 sources): abnormal RR interval, abnormal coping response, abnormal electroretinogram waveform feature, abnormal grip strength, abnormal heart rate, abnormal photoreceptor connecting cilium morphology, abnormal photoreceptor outer segment morphology, abnormal response to new environment, abnormal retina photoreceptor morphology, abnormal sinus arrhythmia, cardiovascular system phenotype, convulsive seizures, decreased a-wave amplitude, decreased b-wave amplitude, decreased coping response, decreased exploration in new environment, decreased heart rate variability, disorganized photoreceptor outer segment, increased a-wave implicit time, increased b-wave implicit time, increased grip strength, increased lean body mass, increased retina apoptosis, increased startle reflex, microgliosis, retina outer nuclear layer degeneration, retina photoreceptor degeneration, shortened RR interval, thin retina outer nuclear layer [+]
View all ortholog results at Monarch