trip13 Phenotypes

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Phenotypes

Gene Literature (0)

Nucleotides (185)

Interactants (124)

XB-GENEPAGE-974897

Gene Symbol: trip13 Gene Name: thyroid hormone receptor interactor 13

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (74 sources): Abdominal pain, Abnormal aortic morphology, Abnormal cardiovascular system morphology, Abnormal lung lobation, Abnormal skull morphology, Abnormality of immune system physiology, Abnormality of skin pigmentation, Abnormality of the orbital region, Abnormality of the skeletal system, Abnormality of the upper limb, Abnormality of vision, Acute lymphoblastic leukemia, Ambiguous genitalia, Aniridia, Aortic regurgitation, Aplasia/Hypoplasia of the cerebellum, Aplasia/Hypoplasia of the corpus callosum, Apnea, Ascites, Atrial septal defect, Cataract, Cleft palate, Clinodactyly of the 5th finger, Coarctation of aorta, Colon cancer, Corneal opacity, Dandy-Walker malformation, Depressed nasal ridge, Downslanted palpebral fissures, Duodenal atresia, Epicanthus, Fever, Frontal bossing, Glaucoma, Global developmental delay, Growth delay, Hearing impairment, Hematuria, High forehead, Holoprosencephaly, Hypertension, Hypothyroidism, Hypotonia, Increased nuchal translucency, Intellectual disability, Intestinal polyposis, Intrauterine growth retardation, Low-set, posteriorly rotated ears, Lymphadenopathy, Microcephaly, Micrognathia, Microphthalmia, Multicystic kidney dysplasia, Multiple cafe-au-lait spots, Muscular dystrophy, Myelodysplasia, Neoplasm, Neoplasm of the liver, Neoplasm of the lung, Nephroblastoma, Osteolysis, Polyhydramnios, Premature chromatid separation, Rhabdomyosarcoma, Seizure, Short stature, Sloping forehead, Stomach cancer, Subvalvular aortic stenosis, Triangular face, Vaginal neoplasm, Ventriculomegaly, Weight loss, Wide nose [+]
Mouse (30 sources): abnormal bone mineralization, abnormal chiasmata formation, abnormal chromosomal synapsis, abnormal double-strand DNA break repair, abnormal female meiosis, abnormal seminiferous tubule morphology, abnormal sinus arrhythmia, abnormal synaptonemal complex, abnormal tail morphology, absent ovarian follicles, arrest of male meiosis, asthenozoospermia, cardiovascular system phenotype, decreased body size, decreased bone mineral content, decreased circulating glucose level, decreased grip strength, decreased heart rate variability, decreased lean body mass, decreased oocyte number, decreased startle reflex, impaired ovarian folliculogenesis, increased fasting circulating glucose level, increased total body fat amount, kinked tail, postnatal lethality, incomplete penetrance, short tail, shortened RR interval, shortened ST segment, small ovary [+]
View all ortholog results at Monarch