Homo sapiens (human): 6006
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Entry
6006 CDS
T01001
Symbol
RHCE, CD240CE, RH, RH30A, RHC, RHCe(152N), RHE, RHIXB, RHNA, RHPI, Rh4, RhIVb(J), RhVI, RhVIII, SLC42A4
Name
(RefSeq) Rh blood group CcEe antigens
KO
K06579
Rhesus blood group glycoprotein
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
]
6006 (RHCE)
04090 CD molecules [BR:
hsa04090
]
6006 (RHCE)
Transporters [BR:
hsa02000
]
Other transporters
Pores ion channels [TC:
1
]
6006 (RHCE)
CD molecules [BR:
hsa04090
]
Proteins
6006 (RHCE)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Ammonium_transp
SLATT_3
MG280
Motif
Other DBs
NCBI-GeneID:
6006
NCBI-ProteinID:
NP_065231
OMIM:
111700
HGNC:
10008
Ensembl:
ENSG00000188672
UniProt:
P18577
A0A220QMN8
Structure
PDB
PDBj
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All DBs
Position
1:complement(25362249..25430203)
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AA seq
417 aa
AA seq
DB search
MSSKYPRSVRRCLPLCALTLEAALILLFYFFTHYDASLEDQKGLVASYQVGQDLTVMAAL
GLGFLTSNFRRHSWSSVAFNLFMLALGVQWAILLDGFLSQFPPGKVVITLFSIRLATMSA
MSVLISAGAVLGKVNLAQLVVMVLVEVTALGTLRMVISNIFNTDYHMNLRHFYVFAAYFG
LTVAWCLPKPLPKGTEDNDQRATIPSLSAMLGALFLWMFWPSVNSALLRSPIQRKNAMFN
TYYALAVSVVTAISGSSLAHPQRKISMTYVHSAVLAGGVAVGTSCHLIPSPWLAMVLGLV
AGLISIGGAKCLPVCCNRVLGIHHISVMHSIFSLLGLLGEITYIVLLVLHTVWNGNGMIG
FQVLLSIGELSLAIVIALTSGLLTGLLLNLKIWKAPHVAKYFDDQVFWKFPHLAVGF
NT seq
1254 nt
NT seq
+upstream
nt +downstream
nt
atgagctctaagtacccgcggtctgtccggcgctgcctgcccctctgcgccctaacactg
gaagcagctctcattctcctcttctatttttttacccactatgacgcttccttagaggat
caaaaggggctcgtggcatcctatcaagtcggccaagatctgaccgtgatggcggccctt
ggcttgggcttcctcacctcaaatttccggagacacagctggagcagtgtggccttcaac
ctcttcatgctggcgcttggtgtgcagtgggcaatcctgctggacggcttcctgagccag
ttccctcctgggaaggtggtcatcacactgttcagtattcggctggccaccatgagtgct
atgtcggtgctgatctcagcgggtgctgtcttggggaaggtcaacttggcgcagttggtg
gtgatggtgctggtggaggtgacagctttaggcaccctgaggatggtcatcagtaatatc
ttcaacacagactaccacatgaacctgaggcacttctacgtgttcgcagcctattttggg
ctgactgtggcctggtgcctgccaaagcctctacccaagggaacggaggataatgatcag
agagcaacgatacccagtttgtctgccatgctgggcgccctcttcttgtggatgttctgg
ccaagtgtcaactctgctctgctgagaagtccaatccaaaggaagaatgccatgttcaac
acctactatgctctagcagtcagtgtggtgacagccatctcagggtcatccttggctcac
ccccaaaggaagatcagcatgacttatgtgcacagtgcggtgttggcaggaggcgtggct
gtgggtacctcgtgtcacctgatcccttctccgtggcttgccatggtgctgggtcttgtg
gctgggctgatctccatcgggggagccaagtgcctgccggtgtgttgtaaccgagtgctg
gggattcaccacatctccgtcatgcactccatcttcagcttgctgggtctgcttggagag
atcacctacattgtgctgctggtgcttcatactgtctggaacggcaatggcatgattggc
ttccaggtcctcctcagcattggggaactcagcttggccatcgtgatagctctcacgtct
ggtctcctgacaggtttgctcctaaatctcaaaatatggaaagcacctcatgtggctaaa
tattttgatgaccaagttttctggaagtttcctcatttggctgttggattttaa
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