KEGG   Homo sapiens (human): 57127
Entry
57127             CDS       T01001                                 
Symbol
RHBG, SLC42A2
Name
(RefSeq) Rh family B glycoprotein
  KO
K06580  ammonium transporter Rh
Organism
hsa  Homo sapiens (human)
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09183 Protein families: signaling and cellular processes
   02000 Transporters [BR:hsa02000]
    57127 (RHBG)
   04090 CD molecules [BR:hsa04090]
    57127 (RHBG)
Transporters [BR:hsa02000]
 Solute carrier family (SLC)
  SLC42: Rh ammonium transporter
   57127 (RHBG)
CD molecules [BR:hsa04090]
 Proteins
  57127 (RHBG)
SSDB
Motif
Pfam: Ammonium_transp GWT1
Other DBs
NCBI-GeneID: 57127
NCBI-ProteinID: NP_065140
OMIM: 607079
HGNC: 14572
Ensembl: ENSG00000132677
UniProt: Q9H310
Position
1:156369211..156385219
AA seq 458 aa
MAGSPSRAAGRRLQLPLLCLFLQGATAVLFAVFVRYNHKTDAALWHRSNHSNADNEFYFR
YPSFQDVHAMVFVGFGFLMVFLQRYGFSSVGFTFLLAAFALQWSTLVQGFLHSFHGGHIH
VGVESMINADFCAGAVLISFGAVLGKTGPTQLLLMALLEVVLFGINEFVLLHLLGVRDAG
GSMTIHTFGAYFGLVLSRVLYRPQLEKSKHRQGSVYHSDLFAMIGTIFLWIFWPSFNAAL
TALGAGQHRTALNTYYSLAASTLGTFALSALVGEDGRLDMVHIQNAALAGGVVVGTSSEM
MLTPFGALAAGFLAGTVSTLGYKFFTPILESKFKVQDTCGVHNLHGMPGVLGALLGVLVA
GLATHEAYGDGLESVFPLIAEGQRSATSQAMHQLFGLFVTLMFASVGGGLGGLLLKLPFL
DSPPDSQHYEDQVHWQVPGEHEDKAQRPLRVEEADTQA
NT seq 1377 nt   +upstreamnt  +downstreamnt
atggccgggtctcctagccgcgccgcgggccggcgactgcagcttcccctgctgtgcctc
ttcctccagggcgccactgccgtcctctttgctgtctttgtccgctacaaccacaaaacc
gacgctgccctctggcaccggagcaaccacagtaacgcggacaatgaattttactttcgc
tacccaagcttccaggacgtgcatgccatggtcttcgtgggctttggcttcctcatggtc
ttcctgcagcgttacggcttcagcagcgtgggcttcaccttcctcctggccgcctttgcc
ctgcagtggtccacactggtccagggctttctccactccttccacggtggccacatccat
gttggcgtggagagcatgatcaatgctgacttttgtgcgggggccgtgctcatctccttt
ggtgccgtcctgggcaagaccgggcctacccagctgctgctcatggccctgctggaggtg
gtgctgtttggcatcaatgagtttgtgctccttcatctcctgggggtgagagatgccgga
ggctccatgactatccacacctttggtgcctacttcgggctcgtcctttcgcgggttctg
tacaggccccagctggagaagagcaagcaccgccagggctccgtctaccattcagacctc
ttcgccatgattgggaccatcttcctgtggatcttctggcctagcttcaatgctgcactc
acagcgctgggggctgggcagcatcggacggccctcaacacatactactccctggctgcc
agcacccttggcacctttgccttgtcagcccttgtaggggaagatgggaggcttgacatg
gtccacatccaaaatgcagcgctggctggaggggttgtggtggggacctcaagtgaaatg
atgctgacaccctttggggctctggcagctggcttcttggctgggactgtctccacgctg
gggtacaagttcttcacgcccatccttgaatcaaaattcaaagtccaagacacatgtgga
gtccacaacctccatgggatgccgggggtcctgggggccctcctgggggtccttgtggct
ggacttgccacccatgaagcttacggagatggcctggagagtgtgtttccactcatagcc
gagggccagcgcagtgccacgtcacaggccatgcaccagctcttcgggctgtttgtcaca
ctgatgtttgcctctgtgggcgggggccttggagggctcctgctgaagctaccctttctg
gactcccccccagactcccagcactacgaggaccaagttcactggcaggtgcctggcgag
catgaggataaagcccagagacctctgagggtggaggaggcagacactcaggcctaa

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Ontology (3)   
   KEGG BRITE (3)   
Disease (1)   
   OMIM (1)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   KEGG ORTHOLOGY (1)   
   RefGene (4)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (1)   
   OC (1)   
Protein sequence (8)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (6)   
DNA sequence (38)   
   RefSeq(nuc) (10)   
   GenBank (14)   
   EMBL (14)   
Protein domain (2)   
   Pfam (2)   
All databases (64)   

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