NP_722477.1
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NCBI GenBank Nucleotide #
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UniProt Primary Accession #
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UniProt Related Accession #
Molecular Weight
61,526 Da
NCBI Official Full Name
protein FAM20A
NCBI Official Synonym Full Names
family with sequence similarity 20, member A
NCBI Official Synonym Symbols
NCBI Protein Information
protein FAM20A; ortholog of human family with sequence similarity 20, member A FAM20A
UniProt Protein Name
Protein FAM20A
UniProt Entry Name
FA20A_MOUSE
UniProt Comments for FAM20A
FAM20A: Defects in FAM20A are the cause of amelogenesis imperfecta and gingival fibromatosis syndrome (AIGFS). An autosomal recessive condition characterized by mild gingival fibromatosis and dental anomalies, including hypoplastic amelogenesis imperfecta, intrapulpal calcifications, delay of tooth eruption, hypodontia/oligodontia, pericoronal radiolucencies, and unerupted teeth. Belongs to the FAM20 family.
Protein type: Secreted, signal peptide; Secreted
Cellular Component: Golgi apparatus; cell; extracellular region
Biological Process: calcium ion homeostasis
Research Articles on FAM20A
Precautions
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Disclaimer
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Diseases associated with FAM20A elisa kit
Organs/Tissues associated with FAM20A elisa kit
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