SLC29A3 蛋白
(Solute Carrier Family 29 Member 3 (SLC29A3))
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].
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3 results
custom-made
SLC29A3
宿主: 人
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, ELISA, SDS
custom-made
SLC29A3
宿主: 小鼠
宿主: Cell-free protein synthesis (CFPS)
Recombinant
approximately 70-80 % as determined by SDS PAGE, Western Blot and analytical SEC (HPLC).
WB, ELISA, SDS
Aliases for SLC29A3 蛋白
solute carrier family 29 member 3 (SLC29A3) 蛋白solute carrier family 29 member 3 (Slc29a3) 蛋白
solute carrier family 29 (nucleoside transporters), member 3 (Slc29a3) 蛋白
solute carrier family 29 (nucleoside transporters), member 3 (SLC29A3) 蛋白
4933435C21Rik 蛋白
AW987637 蛋白
ENT3 蛋白
Ent3 蛋白
HCLAP 蛋白
HJCD 蛋白
PHID 蛋白
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