slc19a3.2 Phenotypes

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Phenotypes

Gene Literature (1)

Nucleotides (76)

Interactants (42)

XB-GENEPAGE-5732457

Gene Symbol: slc19a3.2 Gene Name: solute carrier family 19 member 3 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: slc19a3.2 assayed (7 sources)

Monarch Ortholog Phenotypes These phenotypes are associated with this gene with a has phenotype relation via Monarch.
Human (36 sources): Abnormality of the skin, Aminoaciduria, Anorexia, Arrhythmia, Ataxia, Atrial septal defect, Cardiac arrest, Cardiomyopathy, Cone/cone-rod dystrophy, Congestive heart failure, Cryptorchidism, Diabetes mellitus, Diarrhea, Gastroesophageal reflux, Global developmental delay, Headache, Hoarse voice, Lethargy, Megaloblastic anemia, Nystagmus, Optic atrophy, Pallor, Paresthesia, Paroxysmal atrial tachycardia, Retinal degeneration, Retinal dystrophy, Seizure, Sensorineural hearing impairment, Short stature, Sideroblastic anemia, Situs inversus totalis, Stroke, Thiamine-responsive megaloblastic anemia, Thrombocytopenia, Ventricular septal defect, Visual loss [+]
Mouse (16 sources): abnormal definitive hematopoiesis, abnormal distortion product otoacoustic emission, abnormal erythropoiesis, abnormal myelopoiesis, abnormal spermatid morphology, arrest of male meiosis, cochlear inner hair cell degeneration, cochlear outer hair cell degeneration, decreased erythrocyte cell number, decreased testis weight, digestive/alimentary phenotype, increased insulin sensitivity, increased or absent threshold for auditory brainstem response, increased sensitivity to induced morbidity/mortality, premature death, sensorineural hearing loss [+]
View all ortholog results at Monarch