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SLC19A2
Solute carrier family 19 member 2THTR1, TRMA
This gene encodes the thiamin transporter protein. Mutations in this gene cause thiamin-responsive megaloblastic anemia syndrome (TRMA), which is an autosomal recessive disorder characterized by diabetes mellitus, megaloblastic anemia and sensorineural deafness. Two transcript variants encoding different isoforms have been found for this gene. [provided by RefSeq, Feb 2016]
Top validated antibodies |
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| Invitrogen Antibodies |  PA5-53456 |
1 references | Polyclonal |
IHC
OA
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| antibodies-online | ABIN396527 |
Monoclonal |
WB
EL
IHC
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| Biorbyt | orb1421329 |
Polyclonal |
WB
ICC
IHC
|
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| Novus Biologicals | H00010560-M10 |
Monoclonal |
WB
EL
|
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| Abnova Corporation | H00010560-M10 |
Monoclonal |
WB
EL
|
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