ID   BCI65376; SV 1; linear; mRNA; STD; HUM; 1230 BP.
XX
PA   LC570272.1
XX
DT   23-JUL-2020 (Rel. 144, Created)
DT   09-JUN-2021 (Rel. 144, Last updated, Version 3)
XX
DE   Homo sapiens (human) ammonium transporter Rh type A
XX
KW   .
XX
OS   Homo sapiens (human)
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
XX
RN   [1]
RA   Isa K., Ogasawara K., Tanaka M.;
RT   ;
RL   Submitted (16-JUL-2020) to the INSDC.
RL   Contact:Kazumi Isa Japanese Red Cross Central Blood Institute, Research and
RL   Development; 2-1-67 Tatsumi, Koto-ku, Tokyo 135-8521, Japan
XX
RN   [2]
RA   Tanaka M., Abe T., Minamitani T., Akiba H., Horikawa T., Tobita R., Isa K.,
RA   Ogasawara K., Takahashi H., Tateyama H., Takahashi J., Tone S., Tsumoto K.,
RA   Yasui T., Kimura T., Fujimura Y., Hirayama F., Tani Y., Takihara Y.;
RT   "The Kg-antigen, RhAG with a Lys164Gln mutation, gives rise to hemolytic
RT   disease of the newborn.";
RL   Br. J. Haematol.:(2020).
XX
DR   MD5; f90962f9c07930d7508bc0432028b04a.
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1230
FT                   /organism="Homo sapiens"
FT                   /mol_type="mRNA"
FT                   /country="Japan"
FT                   /db_xref="taxon:9606"
FT   CDS             LC570272.1:35..1264
FT                   /codon_start=1
FT                   /transl_table=1
FT                   /gene="RHAG"
FT                   /product="ammonium transporter Rh type A"
FT                   /protein_id="BCI65376.1"
FT                   /translation="MRFTFPLMAIVLEIAMIVLFGLFVEYETDQTVLEQLNITKPTDMG
FT                   IFFELYPLFQDVHVMIFVGFGFLMTFLKKYGFSSVGINLLVAALGLQWGTIVQGILQSQ
FT                   GQKFNIGIKNMINADFSAATVLISFGAVLGKTSPTQMLIMTILEIVFFAHNEYLVSEIF
FT                   QASDIGASMTIHAFGAYFGLAVAGILYRSGLRKGHENEESAYYSDLFAMIGTLFLWMFW
FT                   PSFNSAIAEPGDKQCRAIVNTYFSLAACVLTAFAFSSLVEHRGKLNMVHIQNATLAGGV
FT                   AVGTCADMAIHPFGSMIIGSIAGMVSVLGYKFLTPLFTTKLRIHDTCGVHNLHGLPGVV
FT                   GGLAGIVAVAMGASNTSMAMQAAALGSSIGTAVVGGLMTGLILKLPLWGQPSDQNCYDD
FT                   SVYWKVPKTR"
XX
SQ   Sequence 1230 BP; 298 A; 276 C; 299 G; 357 T; 0 other;
     atgaggttca cattccctct catggctata gtcctggaaa ttgccatgat tgttttattt        60
     ggattatttg ttgagtatga aacggaccag actgttctcg agcagctcaa catcaccaag       120
     ccaacagaca tgggcatatt ctttgagtta tatcctctgt tccaagatgt acatgttatg       180
     atatttgttg ggtttggctt cctcatgacc ttcctgaaga aatatggctt cagcagtgtg       240
     ggtatcaacc tactcgttgc tgctttgggc ctccagtggg gcactattgt acagggaatc       300
     ctgcaaagcc agggacagaa atttaacatt ggaatcaaaa acatgataaa tgcagacttc       360
     agtgcagcca cagttctgat atcttttgga gctgtcctgg gaaaaacgag ccccacccaa       420
     atgctgatca tgacaatttt agaaattgtt ttctttgccc acaatgaata cctggttagt       480
     gaaatatttc aggcctctga cattggagca tcaatgacga tccatgcctt tggggcctac       540
     tttggcttgg ctgtagcagg catcttgtat cgatctggac tgagaaaggg gcatgaaaat       600
     gaagagtccg catactactc agacttgttt gcaatgattg ggactctctt tctgtggatg       660
     ttttggccca gctttaactc ggccattgct gaacctggag acaaacagtg cagggccatt       720
     gtaaacacgt acttctctct cgctgcctgt gtgctcacag cctttgcctt ctccagccta       780
     gtggagcacc gaggcaagct caacatggtt cacattcaga atgccaccct tgctggagga       840
     gttgctgtgg gcacttgtgc ggatatggca attcacccat ttggttctat gattattggg       900
     agcattgcag gaatggtctc tgtgcttgga tacaagttcc tgactccact ttttactact       960
     aaactgagga tccatgatac atgtggggtc cataacctcc acggcttacc tggtgtagtg      1020
     ggaggccttg caggcattgt ggcagtagca atgggcgcct ccaacacgtc tatggccatg      1080
     caggcagctg cactgggttc ctctatcgga acagcagttg ttggaggtct gatgacaggt      1140
     ttaattctaa agttgcctct ctggggacag ccatctgacc agaactgcta tgatgattct      1200
     gtttattgga aggtccctaa gacgagataa                                       1230
//