Coding: BCI65376.1
Homo sapiens (human) ammonium transporter Rh type A
Accession:
BCI65376
Mol Type:
mRNA
Topology:
linear
Base Count:
1230
Dataclass:
STD
Country:
Japan
Codon Start:
1
Product:
ammonium transporter Rh type A
Protein Id:
BCI65376.1
Transl Table:
1
Publications
Publications in which the generation of this record is described
The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to hemolytic
disease of the newborn. Tanaka M., Abe T., Minamitani T., Akiba H., Horikawa T., Tobita R., Isa K., Ogasawara K., Takahashi H., Tateyama H., Takahashi J., Tone S., Tsumoto K., Yasui T., Kimura T., Fujimura Y., Hirayama F., Tani Y., Takihara Y. |
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