Tissue expression
Cell line expression
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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Invitrogen Antibodies | PA5-38039 | 1 references | Polyclonal |
WB
IHC
OA
|
|
GeneTex | GTX32151 | Polyclonal |
WB
EL
ICC
IHC |
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Boster Biological Technology | A04749 | Polyclonal |
WB
EL
ICC
IHC |
||
Biorbyt | orb1238949 | Polyclonal |
WB
EL
ICC
IHC |
||
ProSci | 8129 | Polyclonal |
WB
ICC
IHC
|
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Supportive data in Antibodypedia
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