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Protein structure
SLC29A3
Solute carrier family 29 member 3ENT3, FLJ11160
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]
Top validated antibodies |
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| GeneTex |  GTX32151 |
Polyclonal |
WB
EL
ICC
IHC
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| Invitrogen Antibodies | PA5-38039 |
1 references | Polyclonal |
WB
IHC
OA
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| Boster Biological Technology | A04749 |
Polyclonal |
WB
EL
ICC
IHC
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| LSBio | LS-C161206 |
Polyclonal |
WB
IHC
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| Biorbyt | orb1238949 |
Polyclonal |
WB
EL
ICC
IHC
|
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