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SLC29A3


Official Full Name
solute carrier family 29 member 3
Organism
Homo sapiens
Gene ID
55315
Background
This gene encodes a nucleoside transporter. The encoded protein plays a role in cellular uptake of nucleosides, nucleobases, and their related analogs. Mutations in this gene have been associated with H syndrome, which is characterized by cutaneous hyperpigmentation and hypertrichosis, hepatosplenomegaly, heart anomalies, and hypogonadism. A related disorder, PHID (pigmented hypertrichosis with insulin-dependent diabetes mellitus), has also been associated with mutations at this locus. Alternatively spliced transcript variants have been described.[provided by RefSeq, Mar 2010]
Synonyms
ENT3; HJCD; PHID; HCLAP

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SHL004992 shRNA set against Rat Slc29a3(NM_181639.3) Inquiry
SHH410172 shRNA set against Human SLC29A3 (NM_018344.5) Inquiry
SHH410176 shRNA set against Mouse SLC29A3 (NM_023596.3) Inquiry
SHH410180 shRNA set against Rat SLC29A3 (NM_181639.3) Inquiry
SHL005408 shRNA set against Mouse Slc29a3(NM_023596.3) Inquiry
Cat.No. Product Name Price
CDFH017837 Human SLC29A3 cDNA Clone(NM_001174098.1) Inquiry
CDFR014997 Rat Slc29a3 cDNA Clone(NM_181639.3) Inquiry
MiUTR1M-10836 SLC29A3 miRNA 3'UTR clone Inquiry
MiUTR1R-07444 SLC29A3 miRNA 3'UTR clone Inquiry
MiUTR3H-12404 SLC29A3 miRNA 3'UTR clone Inquiry
CDCB194706 Rabbit SLC29A3 ORF clone (XM_008269997.1) Inquiry
CDCH081792 human SLC29A3 ORF clone (NM_001174098.1) Inquiry
CDCH081796 Mouse Slc29a3 ORF clone (NM_023596.3) Inquiry
CDCR382044 Rat Slc29a3 ORF Clone(NM_181639.3) Inquiry
CDCS419555 Human SLC29A3 ORF Clone (BC120996) Inquiry
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