Phenotypes
Phenotypic information for the genes in this entry imported from model organism databases.
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Homo sapiens |
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Thyroid hormone organification defect IIA. |
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Total iodide organification defect. |
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Goiter, congenital. |
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Hyperthyroidism, congenital. |
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Mus musculus |
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Life span-post-weaning/aging. |
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Homeostasis/metabolism phenotype. |
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Growth/size phenotype. |
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Endocrine/exocrine gland phenotype. |
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Immune system phenotype. |
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Hematopoietic system phenotype. |
PubMed
Articles associated with genes and sequences of this entry plus additional related articles.
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Mavragani CP, et al.Increased prevalence of antibodies to thyroid peroxidase in dry eyes and mouth syndrome or sicca asthenia polyalgia syndrome. J Rheumatol 36, 1626-30(2009). |
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Simm D, et al.Two novel mutations in the human thyroid peroxidase (TPO) gene: genetics and clinical findings in four children. Acta Paediatr 98, 1057-61(2009). |
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Fuchs O, et al.Congenital hypothyroidism caused by a novel homozygous mutation in the thyroid peroxidase gene. J Pediatr Endocrinol Metab 21, 1093-7(2008). |
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Kessler J, et al.Factors influencing the study of peroxidase-generated iodine species and implications for thyroglobulin synthesis. Thyroid 18, 769-74(2008). |
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Yang M, et al.Thrombopoietin levels increased in patients with severe acute respiratory syndrome. Thromb Res 122, 473-7(2008). |
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Related Homology Resources
Links to curated and computed homology information found in other databases.
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Orthology group for M.musculus Tpo includes H.sapiens TPO and R.norvegicus Tpo. |
UniGene
Links to groups of transcribed sequences established by tblastn searching of UniGene.
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Thyroid peroxidase |
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Similar to thyroid peroxidase |
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Thyroid peroxidase |
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Thyroid peroxidase |
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Thyroid peroxidase |
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Thyroid peroxidase |
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Thyroid peroxidase |
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Thyroid peroxidase |
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