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SAMD9
| Symbol: | SAMD9 | | Name(s): | sterile alpha motif domain containing 9 | | Type: | protein-coding | | Organism: | Homo sapiens | | Synonyms: | C7orf5, FLJ20073, KIAA2004, NFTC, OEF1, OEF2 | | Links: |
Pubmed,
Entrez Gene,
GeneCards,
BioGPS,
Map Viewer.
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Gene Information from Publications |
| Publication Link |
Summary of findings |
| 17507861 |
PIvotal role in calcification and thus implicated in various hereditary diseases such as atherosclerosis, calcinosis and autoimmune diseases. |
| 16960814 |
Mutation analysis revealed a homozygous mutation in the SAMD9 gene (K1495E), which was found to segregate with the disease in all families and to interfere with the protein expression. |
| 17407603 |
SAMD9 and SAMD9L are a novel family of genes, which play a role regulating cell proliferation and suppressing the neoplastic phenotype; the human gene exists in rat, but is lost in mouse, due to a mouse specific rearrangement |
SAMD9 results (if any) from reagent suppliers |
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