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FAM83H, family with sequence similarity 83 member H

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FAM83H, family with sequence similarity 83 member H

  • The protein encoded by this gene plays an important role in the structural development and calcification of tooth enamel. Defects in this gene are a cause of amelogenesis imperfecta type 3 (AI3). [provided by RefSeq, Mar 2010]

  • Gene Synonyms (protein FAM83H, FAM83H variant 1, FAM83H variant 2, truncated FAM83H, AI3, AI3A,)
  • NCBI Gene ID: 286077
  • Species: Homo sapiens (Human)
  • UNIPROT ID#>>Q71RB4
    UNIPROT ID#>>Q6ZRV2
  • View the NCBI Database for this Gene »

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Gene products are often involved in multiple pathways and networks within a living cell. Learn more about other interacting partners.

family with sequence similarity 83 member H interacts with:

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

Paste a protein or nucleic acid sequence in the box below to confirm that it matches this gene’s reference sequence(s). Click on a link under RELATED ORF CLONES to see how a sequence matches to an experimentally-validated ORF clone.

The information on this page was collected from publicly accessible databases, and is periodically updated. Promega makes no claims to accuracy, or ownership of these genes.

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