Homo sapiens Gene: TPO | |||||||||||||||||
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Summary | |||||||||||||||||
InnateDB Gene | IDBG-25524.6 | ||||||||||||||||
Last Modified | 2014-10-13 [Report errors or provide feedback] | ||||||||||||||||
Gene Symbol | TPO | ||||||||||||||||
Gene Name | thyroid peroxidase | ||||||||||||||||
Synonyms | MSA; TDH2A; TPX | ||||||||||||||||
Species | Homo sapiens | ||||||||||||||||
Ensembl Gene | ENSG00000115705 | ||||||||||||||||
Encoded Proteins |
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
thyroid peroxidase
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Protein Structure | |||||||||||||||||
Useful resources | Stemformatics EHFPI ImmGen | ||||||||||||||||
Entrez Gene | |||||||||||||||||
Summary |
This gene encodes a membrane-bound glycoprotein. The encoded protein acts as an enzyme and plays a central role in thyroid gland function. The protein functions in the iodination of tyrosine residues in thyroglobulin and phenoxy-ester formation between pairs of iodinated tyrosines to generate the thyroid hormones, thyroxine and triiodothyronine. Mutations in this gene are associated with several disorders of thyroid hormonogenesis, including congenital hypothyroidism, congenital goiter, and thyroid hormone organification defect IIA. Multiple transcript variants encoding distinct isoforms have been identified for this gene, but the full-length nature of some variants has not been determined. [provided by RefSeq, May 2011] |
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Gene Information | |||||||||||||||||
Type | Protein coding | ||||||||||||||||
Genomic Location | Chromosome 2:1374223-1543711 | ||||||||||||||||
Strand | Forward strand | ||||||||||||||||
Band | p25.3 | ||||||||||||||||
Transcripts | |||||||||||||||||
Interactions | |||||||||||||||||
Number of Interactions |
This gene and/or its encoded proteins are associated with 0 experimentally validated interaction(s) in this database.
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Gene Ontology | |||||||||||||||||
Molecular Function |
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Biological Process |
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Cellular Component |
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Orthologs | |||||||||||||||||
Species
Mus musculus
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Gene ID
Gene Order
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Pathways | |||||||||||||||||
NETPATH | |||||||||||||||||
REACTOME |
Thyroxine biosynthesis pathway
Amine-derived hormones pathway
Metabolism of amino acids and derivatives pathway
Metabolism pathway
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KEGG |
Hematopoietic cell lineage pathway
Cytokine-cytokine receptor interaction pathway
Jak-STAT signaling pathway pathway
Tyrosine metabolism pathway
Autoimmune thyroid disease pathway
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INOH | |||||||||||||||||
PID NCI | |||||||||||||||||
Cross-References | |||||||||||||||||
SwissProt | |||||||||||||||||
TrEMBL | |||||||||||||||||
UniProt Splice Variant | |||||||||||||||||
Entrez Gene | |||||||||||||||||
UniGene | Hs.467554 Hs.598371 Hs.735569 | ||||||||||||||||
RefSeq | NM_000547 NM_001206744 NM_001206745 NM_175719 NM_175721 NM_175722 XM_005264699 XM_005264701 XM_005264702 | ||||||||||||||||
HUGO | |||||||||||||||||
OMIM | |||||||||||||||||
CCDS | CCDS1643 CCDS1644 CCDS1646 | ||||||||||||||||
HPRD | 06000 | ||||||||||||||||
IMGT | |||||||||||||||||
EMBL | |||||||||||||||||
GenPept | |||||||||||||||||
RNA Seq Atlas | |||||||||||||||||