ttc8 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (82)

Interactants (36)

XB-GENEPAGE-1000121

Gene Symbol: ttc8 Gene Name: tetratricopeptide repeat domain 8

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (56 sources): Abnormal electroretinogram, Abnormality of fundus pigmentation, Abnormality of retinal pigmentation, Abnormal retinal vascular morphology, Abnormal speech pattern, Abnormal testis morphology, Anteverted nares, Atypical scarring of skin, Blindness, Brachycephaly, Cataract, Cognitive impairment, Conductive hearing impairment, Constriction of peripheral visual field, Cryptorchidism, Downslanted palpebral fissures, Finger syndactyly, Generalized hirsutism, Glaucoma, Global developmental delay, Hearing impairment, Hepatic fibrosis, Hyperinsulinemia, Hyperreflexia, Hypertension, Hypogonadism, Hypoplasia of penis, Hypoplasia of the ovary, Hypospadias, Intellectual disability, Keratoconus, Medial flaring of the eyebrow, Multicystic kidney dysplasia, Nephrotic syndrome, Nyctalopia, Nystagmus, Obesity, obsolete Low-set, posteriorly rotated ears, Ophthalmoplegia, Optic atrophy, Photophobia, Pigmentary retinopathy, Polydactyly, Postaxial hand polydactyly, Progressive night blindness, Prominent nasal bridge, Renal dysplasia, Rod-cone dystrophy, Sensorineural hearing impairment, Short neck, Short stature, Situs inversus totalis, Skeletal muscle atrophy, Type II diabetes mellitus, Visual impairment, Wide nasal bridge [+]
Mouse (7 sources): abnormal olfactory epithelium cilium morphology, abnormal photoreceptor inner segment morphology, decreased body size, dilated renal tubules, impaired olfaction, postnatal lethality, incomplete penetrance, slow postnatal weight gain
View all ortholog results at Monarch