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SAMD9L


Official Full Name
sterile alpha motif domain containing 9 like
Organism
Homo sapiens
Gene ID
219285
Background
This gene encodes a cytoplasmic protein that acts as a tumor suppressor but also plays a key role in cell proliferation and the innate immune response to viral infection. The encoded protein contains an N-terminal sterile alpha motif domain. Naturally occurring mutations in this gene are associated with myeloid disorders such as juvenile myelomonocytic leukemia, acute myeloid leukemia, and myelodysplastic syndrome. Naturally occurring mutations are also associated with hepatitis-B related hepatocellular carcinoma, normophosphatemic familial tumoral calcinosis, and ataxia-pancytopenia syndrome. [provided by RefSeq, Apr 2017]
Synonyms
UEF1; ATXPC; DEL7q; DRIF2; MLSM7; SCA49; C7DELq; C7orf6; M7MLS1

Cat.No. Product Name Price
SHH401720 shRNA set against Human SAMD9L (NM_152703.2) Inquiry
Cat.No. Product Name Price
CDFG009687 Human SAMD9L cDNA Clone(NM_152703.2) Inquiry
CDFG009690 Human SAMD9L cDNA Clone(NM_152703.2) Inquiry
CDFL011901 Mouse Samd9l cDNA Clone(NM_010156.3) Inquiry
MiUTR1H-09134 SAMD9L miRNA 3'UTR clone Inquiry
CDCB185615 Rabbit SAMD9L ORF clone (XM_008261728.1) Inquiry
CDCH076830 human SAMD9L ORF clone (NM_152703.2) Inquiry
CDCH076836 Mouse Samd9l ORF clone (NM_010156.3) Inquiry
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