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UniProtKB/Swiss-Prot entry P18577


[Entry info] [Name and origin] [References] [Comments] [Cross-references] [Keywords] [Features] [Sequence] [Tools]

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Entry information
Entry name RHCE_HUMAN
Primary accession number P18577
Secondary accession numbers A7DW68 B7UDF3 B7UDF4 B7UDF5 B7UDF6 B7UDF7 B7UDF8 B7UDF9 B7UDG0 B7UDG1 B7UDG2 B7UDG3 Q02163 Q02164 Q02165 Q16160 Q2MJW0 Q2VC86 Q3LTM6 Q6AZX5 Q6J2U3 Q7RU06 Q8IZT2 Q8IZT3 Q8IZT4 Q8IZT5 Q9UD13 Q9UD14 Q9UD15 Q9UD16 Q9UEC2 Q9UEC3 Q9UPN0
Integrated into Swiss-Prot on November 1, 1990
Sequence was last modified on January 23, 2007 (Sequence version 2)
Annotations were last modified on    June 16, 2009 (Entry version 91)
Name and origin of the protein
Protein name Blood group Rh(CE) polypeptide
Synonyms Rhesus C/E antigens
Rh30A
RhIXB
Rh polypeptide 1
RhPI
CD240CE antigen
Gene name
Name: RHCE
Synonyms: RHC, RHE
From
Homo sapiens (Human) [TaxID: 9606] 
Taxonomy Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; Homo.
Protein existence 1: Evidence at protein level;
References
[1]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI).
PubMed=2123099 [NCBI, ExPASy, EBI, Israel, Japan]
Avent N.D., Ridgwell K., Tanner M.J.A., Anstee D.J.;
"cDNA cloning of a 30 kDa erythrocyte membrane protein associated with Rh (Rhesus)-blood-group-antigen expression.";
Biochem. J. 271:821-825(1990).
[2]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND PARTIAL PROTEIN SEQUENCE.
TISSUE=Bone marrow;
DOI=10.1073/pnas.87.16.6243; PubMed=1696722 [NCBI, ExPASy, EBI, Israel, Japan]
Cherif-Zahar B., Bloy C., le van Kim C., Blanchard D., Bailly P., Hermand P., Salmon C., Cartron J.-P., Colin Y.;
"Molecular cloning and protein structure of a human blood group Rh polypeptide.";
Proc. Natl. Acad. Sci. U.S.A. 87:6243-6247(1990).
[3]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORMS RHIV; RHVI AND RHVIII).
TISSUE=Bone marrow;
PubMed=1379850 [NCBI, ExPASy, EBI, Israel, Japan]
le van Kim C., Cherif-Zahar B., Raynal V., Mouro I., Lopez M., Cartron J.-P., Colin Y.;
"Multiple Rh messenger RNA isoforms are produced by alternative splicing.";
Blood 80:1074-1078(1992).
[4]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI).
DOI=10.1007/BF00222717; PubMed=7916743 [NCBI, ExPASy, EBI, Israel, Japan]
Kajii E., Umenishi F., Iwamoto S., Ikemoto S.;
"Isolation of a new cDNA clone encoding an Rh polypeptide associated with the Rh blood group system.";
Hum. Genet. 91:157-162(1993).
[5]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), VARIANT CYS-16, AND VARIANT E/RH5 ANTIGEN ALA-226.
DOI=10.1046/j.1365-2141.2001.02803.x; PubMed=11380456 [NCBI, ExPASy, EBI, Israel, Japan]
Westhoff C.M., Silberstein L.E., Wylie D.E., Skavdahl M., Reid M.E.;
"16Cys encoded by the RHce gene is associated with altered expression of the e antigen and is frequent in the R0 haplotype.";
Br. J. Haematol. 113:666-671(2001).
[6]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANTS ILE-60; SER-68; SER-103; VAL-127; ASP-128; RHEKH THR-154; RHEFM GLU-233 AND RHEFM VAL-238.
DOI=10.1046/j.1537-2995.2001.41111408.x; PubMed=11724987 [NCBI, ExPASy, EBI, Israel, Japan]
Kashiwase K., Ishikawa Y., Hyodo H., Watanabe Y., Ogawa A., Tsuneyama H., Toyoda C., Uchikawa M., Akaza T., Omine M., Juji T.;
"E variants found in Japanese and c antigenicity alteration without substitution in the second extracellular loop.";
Transfusion 41:1408-1412(2001).
[7]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANTS CYS-16; ALA-226; VAL-238; VAL-245; GLY-263 AND LYS-267.
DOI=10.1182/blood-2002-01-0229; PubMed=12393640 [NCBI, ExPASy, EBI, Israel, Japan]
Noizat-Pirenne F., Lee K., Le Pennec P.-Y., Simon P., Kazup P., Bachir D., Rouzaud A.M., Roussel M., Juszczak G., Menanteau C., Rouger P., Kotb R., Cartron J.-P., Ansart-Pirenne H.;
"Rare RHCE phenotypes in black individuals of Afro-Caribbean origin: identification and transfusion safety.";
Blood 100:4223-4231(2002).
[8]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANTS CYS-16; ILE-60; SER-68; SER-103 AND ALA-226.
Yan L., Xu X., Zhu F.;
"A new RhCe allele in Chinese Han population.";
Submitted (APR-2004) to the EMBL/GenBank/DDBJ databases.
[9]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANTS CYS-16; ALA-226; GLU-233 AND VAL-245.
Westhoff C.M., Vege S.;
"Molecular basis for Crawford antigen expression.";
Submitted (AUG-2005) to the EMBL/GenBank/DDBJ databases.
[10]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANTS CYS-16; ILE-60; SER-68 AND SER-103.
Vege S., Westhoff C.M.;
"RHCE gene, allele CE, antigen CE.";
Submitted (OCT-2005) to the EMBL/GenBank/DDBJ databases.
[11]
NUCLEOTIDE SEQUENCE [MRNA] (ISOFORM RHI), AND VARIANT ALA-226.
Westhoff C.M., Vege S.;
"RHCE gene, allele RHce, ce antigen.";
Submitted (DEC-2005) to the EMBL/GenBank/DDBJ databases.
[12]
NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS CYS-16; ILE-60; SER-68; SER-103; ALA-226 AND GLU-398.
Wei Q., Flegel W.A.;
"RHD allele and RH haplotype distribution in Tibetans.";
Submitted (AUG-2006) to the EMBL/GenBank/DDBJ databases.
[13]
NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS CYS-16; ILE-60; SER-68; SER-103; ALA-226 AND LYS-267.
Bugert P., Scharberg E.A., Geisen C., von Zabern I., Flegel W.A.;
Submitted (NOV-2008) to the EMBL/GenBank/DDBJ databases.
[14]
NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA], AND VARIANTS CYS-16 AND ALA-226.
DOI=10.1038/nature04727; PubMed=16710414 [NCBI, ExPASy, EBI, Israel, Japan]
Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A., Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C., Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K., Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C., Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W., Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J., Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J., Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y., Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J., Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H., Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L., Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J., Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S., Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K., Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R., Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M., Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S., Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J., Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W., McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N., Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V., Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J., Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E., Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S., Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M., White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H., Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E., Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G., Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.;
"The DNA sequence and biological annotation of human chromosome 1.";
Nature 441:315-321(2006).
[15]
NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA] (ISOFORM RHI), AND VARIANTS CYS-16; ILE-60; SER-68; SER-103 AND ALA-226.
TISSUE=Brain;
DOI=10.1101/gr.2596504; PubMed=15489334 [NCBI, ExPASy, EBI, Israel, Japan]
The MGC Project Team;
"The status, quality, and expansion of the NIH full-length cDNA project: the Mammalian Gene Collection (MGC).";
Genome Res. 14:2121-2127(2004).
[16]
NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 1-11.
DOI=10.1006/geno.1994.1014; PubMed=8188244 [NCBI, ExPASy, EBI, Israel, Japan]
Cherif-Zahar B., le van Kim C., Rouillac C., Raynal V., Cartron J.-P., Colin Y.;
"Organization of the gene (RHCE) encoding the human blood group RhCcEe antigens and characterization of the promoter region.";
Genomics 19:68-74(1994).
[17]
PROTEIN SEQUENCE OF 2-33.
PubMed=3146980 [NCBI, ExPASy, EBI, Israel, Japan]
Avent N.D., Ridgwell K., Mawby W.J., Tanner M.J.A., Anstee D.J., Kumpel B.;
"Protein-sequence studies on Rh-related polypeptides suggest the presence of at least two groups of proteins which associate in the human red-cell membrane.";
Biochem. J. 256:1043-1046(1988).
[18]
PROTEIN SEQUENCE OF 2-17.
PubMed=3135863 [NCBI, ExPASy, EBI, Israel, Japan]
Bloy C., Blanchard D., Dahr W., Beyreuther K., Salmon C., Cartron J.-P.;
"Determination of the N-terminal sequence of human red cell Rh(D) polypeptide and demonstration that the Rh(D), (c), and (E) antigens are carried by distinct polypeptide chains.";
Blood 72:661-666(1988).
[19]
NUCLEOTIDE SEQUENCE [MRNA] OF 141-417 (ISOFORMS 1C; 1D; 1H; 2E; 4G; 7A; 8A; 8E; 8H; RHIV AND RHVI), AND ALTERNATIVE SPLICING.
TISSUE=Blood;
DOI=10.1007/BF00209483; PubMed=7789951 [NCBI, ExPASy, EBI, Israel, Japan]
Kajii E., Umenishi F., Omi T., Ikemoto S.;
"Intricate combinatorial patterns of exon splicing generate multiple Rh-related isoforms in human erythroid cells.";
Hum. Genet. 95:657-665(1995).
[20]
PROTEIN SEQUENCE OF 402-409.
PubMed=1898705 [NCBI, ExPASy, EBI, Israel, Japan]
Suyama K., Goldstein J., Aebersold R., Kent S.;
"Regarding the size of Rh proteins.";
Blood 77:411-411(1991).
[21]
IDENTIFICATION, AND VARIANTS CYS-16 AND ALA-226.
DOI=10.1182/blood-2001-12-0153; PubMed=11902138 [NCBI, ExPASy, EBI, Israel, Japan]
Wagner F.F., Flegel W.A.;
"RHCE represents the ancestral RH position, while RHD is the duplicated gene.";
Blood 99:2272-2273(2002).
[22]
VARIANTS BLOOD GROUP C AND E.
DOI=10.1038/ng0993-62; PubMed=8220426 [NCBI, ExPASy, EBI, Israel, Japan]
Mouro I., Colin Y., Cherif-Zahar B., Cartron J.-P., le van Kim C.;
"Molecular genetic basis of the human Rhesus blood group system.";
Nat. Genet. 5:62-65(1993).
Comments
Copyright
Copyrighted by the UniProt Consortium, see http://www.uniprot.org/terms. Distributed under the Creative Commons Attribution-NoDerivs License.
Cross-references
Sequence databases
EMBL
X54534; CAA38401.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
M34015; AAA36567.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
X63095; CAA44809.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
X63096; CAA44810.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
X63098; CAA44812.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
S57967; AAB26080.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
DQ266400; ABB69097.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AB018644; BAA33927.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AB018645; BAA33928.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AB030388; BAA82627.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AB049753; BAB16597.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AF510065; AAN75121.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AF510066; AAN75122.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AF510067; AAN75123.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AF510068; AAN75124.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AY603478; AAT35811.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
DQ178642; ABA25912.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
DQ266353; ABB97471.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
DQ322275; ABC55358.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AM398146; CAL44958.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486155; ACK75562.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486156; ACK75563.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486157; ACK75564.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486158; ACK75565.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486159; ACK75566.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486160; ACK75567.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486161; ACK75568.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486162; ACK75569.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486163; ACK75570.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486164; ACK75571.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
FJ486165; ACK75572.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AL031284; CAM12858.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AL928711; CAM12858.1; JOINED; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AL928711; CAH72605.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
AL031284; CAH72605.1; JOINED; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
BC075081; AAH75081.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
BC139905; AAI39906.1; -; mRNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
S70456; AAD14061.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
BN000065; CAD29850.1; -; Genomic_DNA.[EMBL / GenBank / DDBJ] [CoDingSequence]
IPI IPI00221016; -.
IPI00334938; -.
IPI00465155; -.
IPI00719561; -.
IPI00827862; -.
IPI00896457; -.
PIR A30405; A30405.
I54193; I54193.
S78478; S78478.
S78479; S78479.
S78480; S78480.
RefSeq NP_065231.2; -.
NP_619522.2; -.
NP_619523.2; -.
NP_619524.2; -.
UniGene Hs.449968
3D structure databases
ModBase P18577.
Protein family/group databases
TCDB 1.A.11.4.3; ammonia transporter channel (Amt) family.
Organism-specific databases
GeneCards GC01M025561; -.
H-InvDB HIX0023511; -.
HGNC HGNC:10008; RHCE.
GenAtlas RHCE.
MIM 111690; phenotype. [NCBI / EBI]
111700; gene+phenotype. [NCBI / EBI]
Orphanet 71275; Rh deficiency syndrome.
PharmGKB PA34386; -.
Gene expression databases
ArrayExpress P18577; -.
Bgee P18577; -.
CleanEx HS_RHCE; -.
GermOnline ENSG00000188672; Homo sapiens.
Ontologies
GO
GO:0005887; Cellular component: integral to plasma membrane (traceable author statement from ProtInc).
GO:0008519; Molecular function: ammonium transmembrane transporter activity (inferred from electronic annotation from InterPro).
GO:0006810; Biological process: transport (inferred from electronic annotation from InterPro).
QuickGo view.
Family and domain databases
InterPro IPR001905; Ammonium_transpt.
IPR002229; RhesusRHD.
Graphical view of domain structure.
Pfam PF00909; Ammonium_transp; 1.
Pfam graphical view of domain structure.
PRINTS PR00342; RHESUSRHD.
Genome annotation databases
Ensembl ENSG00000188672; Homo sapiens. [Contig view]
GeneID 6006; -.
KEGG hsa:6006; -.
Phylogenomic databases
HOVERGEN P18577; -.
Other
NextBio 23427; -.
SOURCE RHCE; Homo sapiens.
ProtoNet P18577.
UniRef View cluster of proteins with at least 50% / 90% / 100% identity.
Keywords
Alternative splicing; Blood group antigen; Direct protein sequencing; Membrane; Polymorphism; Transmembrane.
Features
SEVIEWER logo Feature table viewer FT aligner logo Feature aligner
KeyFrom   To Length Description FTId
INIT_MET   1     1        Removed. 
CHAIN   2   417  416     Blood group Rh(CE) polypeptide. PRO_0000168189
TRANSMEM   12    32  21     Potential. 
TRANSMEM   44    64  21     Potential. 
TRANSMEM   77    97  21     Potential. 
TRANSMEM   125   145  21     Potential. 
TRANSMEM   172   192  21     Potential. 
TRANSMEM   203   223  21     Potential. 
TRANSMEM   238   258  21     Potential. 
TRANSMEM   265   285  21     Potential. 
TRANSMEM   287   307  21     Potential. 
TRANSMEM   331   351  21     Potential. 
TRANSMEM   358   378  21     Potential. 
VAR_SEQ   163   409        Missing (in isoform 8h). VSP_037505
VAR_SEQ   163   313        Missing (in isoform RHVIII). VSP_005701
VAR_SEQ   163   220        Missing (in isoform 8a). VSP_037506
VAR_SEQ   163   203        TDYHMNLRHFYVFAAYFGLTVAWCLPKPLPKGTEDN DQRAT -> DWLPGPPQHWGTQLGHRDSSHVWSPDRFAPKSQNME STSCG (in isoform 8e). VSP_037507
VAR_SEQ   164   268        Missing (in isoform RHVI and isoform 7a). VSP_005702
VAR_SEQ   204   417        Missing (in isoform 8e). VSP_037508
VAR_SEQ   212   384        Missing (in isoform 4g). VSP_037509
VAR_SEQ   268   308        TYVHSAVLAGGVAVGTSCHLIPSPWLAMVLGLVAGL ISIGG -> DWLPGPPQHWGTQLGHRDSSHVWSPDRFAPKSQNME STSCG (in isoform 2e). VSP_037510
VAR_SEQ   301   313        Missing (in isoform 8a). VSP_037511
VAR_SEQ   309   417        Missing (in isoform 2e). VSP_037512
VAR_SEQ   314   409        Missing (in isoform 1h). VSP_037513
VAR_SEQ   314   354        VCCNRVLGIHHISVMHSIFSLLGLLGEITYIVLLVL HTVWN -> DWLPGPPQHWGTQLGHRDSSHVWSPDRFAPKSQNME STSCG (in isoform RHIV). VSP_005703
VAR_SEQ   355   417        Missing (in isoform RHIV). VSP_005704
VAR_SEQ   358   417        MIGFQVLLSIGELSLAIVIALTSGLLTGLLLNLKIWKAPH VAKYFDDQVFWKFPHLAVGF -> IFLIWLLDFKQKHPRKTRPVQKQDNFLSLLPAVREKRS (in isoform 1d). VSP_037514
VAR_SEQ   359   417        IGFQVLLSIGELSLAIVIALTSGLLTGLLLNLKIWKAPHV AKYFDDQVFWKFPHLAVGF -> FAPKSQNMESTSC (in isoform RHVI and isoform 1c). VSP_005705
VARIANT   16    16  1     W -> C (associated with altered expression of E antigen). VAR_006911 
VARIANT   36    36  1     A -> T (in C(X)/Rh9 antigen). VAR_006912 
VARIANT   41    41  1     Q -> R (in C(W)/Rh8 antigen). VAR_006913 
VARIANT   60    60  1     L -> I. VAR_006914 
VARIANT   68    68  1     N -> S (in dbSNP:rs1053344 [NCBI]). VAR_006915 
VARIANT   103   103  1     P -> S (in C/Rh2 antigen; dbSNP:rs676785 [NCBI]). VAR_006916 
VARIANT   127   127  1     A -> V (in dbSNP:rs1053346 [NCBI]). VAR_055260 
VARIANT   128   128  1     G -> D (in dbSNP:rs1053347 [NCBI]). VAR_055261 
VARIANT   154   154  1     R -> T (in RhEKH). VAR_013301 
VARIANT   182   182  1     T -> S (in dbSNP:rs1053350 [NCBI]). VAR_055262 
VARIANT   198   198  1     N -> K (in dbSNP:rs1053354 [NCBI]). VAR_055263 
VARIANT   226   226  1     P -> A (in E/Rh5 antigen; dbSNP:rs609320 [NCBI]). VAR_006917 
VARIANT   233   233  1     Q -> E (in RhEFM). VAR_013302 
VARIANT   238   238  1     M -> V (in RhEFM). VAR_013303 
VARIANT   245   245  1     L -> V (in VS antigen; dbSNP:rs1053361 [NCBI]). VAR_006918 
VARIANT   263   263  1     R -> G (in dbSNP:rs1132763 [NCBI]). VAR_057987 
VARIANT   267   267  1     M -> K (in dbSNP:rs1132764 [NCBI]). VAR_057988 
VARIANT   323   323  1     H -> P (in dbSNP:rs1053366 [NCBI]). VAR_055264 
VARIANT   325   325  1     I -> S (in dbSNP:rs1053367 [NCBI]). VAR_055265 
VARIANT   329   329  1     H -> D (in dbSNP:rs1053370 [NCBI]). VAR_055266 
VARIANT   329   329  1     H -> R (in dbSNP:rs1053371 [NCBI]). VAR_055267 
VARIANT   330   330  1     S -> Y (in dbSNP:rs1053372 [NCBI]). VAR_055268 
VARIANT   331   331  1     I -> N (in dbSNP:rs1053373 [NCBI]). VAR_055269 
VARIANT   398   398  1     V -> E (in dbSNP:rs630612 [NCBI]). VAR_057989 
CONFLICT   10    10        R -> W (in Ref. 13; ACK75562). 
CONFLICT   12    12        C -> L (in Ref. 18; AA sequence). 
CONFLICT   53    53        D -> G (in Ref. 3; CAA44812). 
CONFLICT   61    61        G -> C (in Ref. 3; CAA44812). 
CONFLICT   114   114        R -> W (in Ref. 7; AAN75123). 
CONFLICT   115   115        L -> P (in Ref. 13; ACK75563/ACK75565). 
CONFLICT   121   121        M -> L (in Ref. 6; BAB16597/BAA82627). 
CONFLICT   122   122        S -> P (in Ref. 13; ACK75564). 
CONFLICT   125   125        I -> N (in Ref. 13; ACK75565). 
CONFLICT   152   152        T -> N (in Ref. 6; BAB16597/BAA82627). 
CONFLICT   155   155        M -> V (in Ref. 8; AAT35811). 
CONFLICT   166   166        H -> L (in Ref. 13; ACK75566). 
CONFLICT   169   169        L -> Q (in Ref. 13; ACK75567). 
CONFLICT   201   201        R -> T (in Ref. 13; ACK75568). 
CONFLICT   217   217        W -> R (in Ref. 13; ACK75569). 
CONFLICT   241   241        T -> I (in Ref. 13; ACK75570). 
CONFLICT   250   250        V -> M (in Ref. 7; AAN75124). 
CONFLICT   273   273        A -> V (in Ref. 7; AAN75122). 
CONFLICT   303   303        L -> Q (in Ref. 13; ACK75572). 
CONFLICT   378   378        L -> V (in Ref. 7; AAN75122). 
CONFLICT   408   409        WK -> DI (in Ref. 20; AA sequence). 
Sequence information
Length: 417 AA [This is the length of the unprocessed precursor] Molecular weight: 45560 Da [This is the MW of the unprocessed precursor] CRC64: 29D33E778D9053DF [This is a checksum on the sequence]
        10         20         30         40         50         60 
MSSKYPRSVR RCLPLWALTL EAALILLFYF FTHYDASLED QKGLVASYQV GQDLTVMAAL 

        70         80         90        100        110        120 
GLGFLTSNFR RHSWSSVAFN LFMLALGVQW AILLDGFLSQ FPPGKVVITL FSIRLATMSA 

       130        140        150        160        170        180 
MSVLISAGAV LGKVNLAQLV VMVLVEVTAL GTLRMVISNI FNTDYHMNLR HFYVFAAYFG 

       190        200        210        220        230        240 
LTVAWCLPKP LPKGTEDNDQ RATIPSLSAM LGALFLWMFW PSVNSPLLRS PIQRKNAMFN 

       250        260        270        280        290        300 
TYYALAVSVV TAISGSSLAH PQRKISMTYV HSAVLAGGVA VGTSCHLIPS PWLAMVLGLV 

       310        320        330        340        350        360 
AGLISIGGAK CLPVCCNRVL GIHHISVMHS IFSLLGLLGE ITYIVLLVLH TVWNGNGMIG 

       370        380        390        400        410 
FQVLLSIGEL SLAIVIALTS GLLTGLLLNL KIWKAPHVAK YFDDQVFWKF PHLAVGF 

P18577 in FASTA format

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Tools Sequence analysis tools: ProtParam, ProtScale, Compute pI/Mw, PeptideMass, PeptideCutter, Dotlet (Java)
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