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ERMAP_HUMAN
ID   ERMAP_HUMAN             Reviewed;         475 AA.
AC   Q96PL5; D3DPW8; Q5VV53; Q6DUE0; Q7Z3X0; Q8NCV8; Q8NCW2; Q8NCW3; Q96PL6;
DT   07-MAR-2006, integrated into UniProtKB/Swiss-Prot.
DT   01-DEC-2001, sequence version 1.
DT   03-AUG-2022, entry version 168.
DE   RecName: Full=Erythroid membrane-associated protein;
DE            Short=hERMAP;
DE   AltName: Full=Radin blood group antigen;
DE   AltName: Full=Scianna blood group antigen;
DE   Flags: Precursor;
GN   Name=ERMAP; Synonyms=RD, SC;
OS   Homo sapiens (Human).
OC   Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia;
OC   Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae;
OC   Homo.
OX   NCBI_TaxID=9606;
RN   [1]
RP   NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, AND DEVELOPMENTAL STAGE.
RC   TISSUE=Fetal liver;
RX   PubMed=11783959; DOI=10.1006/bcmd.2001.0465;
RA   Su Y.-Y., Gordon C.T., Ye T.-Z., Perkins A.C., Chui D.H.K.;
RT   "Human ERMAP: an erythroid adhesion/receptor transmembrane protein.";
RL   Blood Cells Mol. Dis. 27:938-949(2001).
RN   [2]
RP   NUCLEOTIDE SEQUENCE [MRNA], TISSUE SPECIFICITY, DEVELOPMENTAL STAGE, AND
RP   SUBCELLULAR LOCATION.
RC   TISSUE=Fetal liver;
RX   PubMed=11549310; DOI=10.1006/geno.2001.6600;
RA   Xu H., Foltz L., Sha Y., Madlansacay M.R., Cain C., Lindemann G.,
RA   Vargas J., Nagy D., Harriman B., Mahoney W., Schueler P.A.;
RT   "Cloning and characterization of human erythroid membrane-associated
RT   protein, human ERMAP.";
RL   Genomics 76:2-4(2001).
RN   [3]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] (ALLELE SC-3), POLYMORPHISM, VARIANTS
RP   BLOOD GROUP SC2 ARG-57 AND SC4 ALA-60, AND VARIANT TYR-26.
RX   PubMed=12393480; DOI=10.1182/blood-2002-07-2064;
RA   Wagner F.F., Poole J., Flegel W.A.;
RT   "Scianna antigens including Rd are expressed by ERMAP.";
RL   Blood 101:752-757(2003).
RN   [4]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RC   TISSUE=Uterus;
RX   PubMed=17974005; DOI=10.1186/1471-2164-8-399;
RA   Bechtel S., Rosenfelder H., Duda A., Schmidt C.P., Ernst U.,
RA   Wellenreuther R., Mehrle A., Schuster C., Bahr A., Bloecker H., Heubner D.,
RA   Hoerlein A., Michel G., Wedler H., Koehrer K., Ottenwaelder B., Poustka A.,
RA   Wiemann S., Schupp I.;
RT   "The full-ORF clone resource of the German cDNA consortium.";
RL   BMC Genomics 8:399-399(2007).
RN   [5]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA], AND VARIANTS VAL-4; TYR-26; ARG-259 AND
RP   GLU-263.
RG   SeattleSNPs variation discovery resource;
RL   Submitted (JUN-2005) to the EMBL/GenBank/DDBJ databases.
RN   [6]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RX   PubMed=16710414; DOI=10.1038/nature04727;
RA   Gregory S.G., Barlow K.F., McLay K.E., Kaul R., Swarbreck D., Dunham A.,
RA   Scott C.E., Howe K.L., Woodfine K., Spencer C.C.A., Jones M.C., Gillson C.,
RA   Searle S., Zhou Y., Kokocinski F., McDonald L., Evans R., Phillips K.,
RA   Atkinson A., Cooper R., Jones C., Hall R.E., Andrews T.D., Lloyd C.,
RA   Ainscough R., Almeida J.P., Ambrose K.D., Anderson F., Andrew R.W.,
RA   Ashwell R.I.S., Aubin K., Babbage A.K., Bagguley C.L., Bailey J.,
RA   Beasley H., Bethel G., Bird C.P., Bray-Allen S., Brown J.Y., Brown A.J.,
RA   Buckley D., Burton J., Bye J., Carder C., Chapman J.C., Clark S.Y.,
RA   Clarke G., Clee C., Cobley V., Collier R.E., Corby N., Coville G.J.,
RA   Davies J., Deadman R., Dunn M., Earthrowl M., Ellington A.G., Errington H.,
RA   Frankish A., Frankland J., French L., Garner P., Garnett J., Gay L.,
RA   Ghori M.R.J., Gibson R., Gilby L.M., Gillett W., Glithero R.J.,
RA   Grafham D.V., Griffiths C., Griffiths-Jones S., Grocock R., Hammond S.,
RA   Harrison E.S.I., Hart E., Haugen E., Heath P.D., Holmes S., Holt K.,
RA   Howden P.J., Hunt A.R., Hunt S.E., Hunter G., Isherwood J., James R.,
RA   Johnson C., Johnson D., Joy A., Kay M., Kershaw J.K., Kibukawa M.,
RA   Kimberley A.M., King A., Knights A.J., Lad H., Laird G., Lawlor S.,
RA   Leongamornlert D.A., Lloyd D.M., Loveland J., Lovell J., Lush M.J.,
RA   Lyne R., Martin S., Mashreghi-Mohammadi M., Matthews L., Matthews N.S.W.,
RA   McLaren S., Milne S., Mistry S., Moore M.J.F., Nickerson T., O'Dell C.N.,
RA   Oliver K., Palmeiri A., Palmer S.A., Parker A., Patel D., Pearce A.V.,
RA   Peck A.I., Pelan S., Phelps K., Phillimore B.J., Plumb R., Rajan J.,
RA   Raymond C., Rouse G., Saenphimmachak C., Sehra H.K., Sheridan E.,
RA   Shownkeen R., Sims S., Skuce C.D., Smith M., Steward C., Subramanian S.,
RA   Sycamore N., Tracey A., Tromans A., Van Helmond Z., Wall M., Wallis J.M.,
RA   White S., Whitehead S.L., Wilkinson J.E., Willey D.L., Williams H.,
RA   Wilming L., Wray P.W., Wu Z., Coulson A., Vaudin M., Sulston J.E.,
RA   Durbin R.M., Hubbard T., Wooster R., Dunham I., Carter N.P., McVean G.,
RA   Ross M.T., Harrow J., Olson M.V., Beck S., Rogers J., Bentley D.R.;
RT   "The DNA sequence and biological annotation of human chromosome 1.";
RL   Nature 441:315-321(2006).
RN   [7]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE GENOMIC DNA].
RA   Mural R.J., Istrail S., Sutton G.G., Florea L., Halpern A.L., Mobarry C.M.,
RA   Lippert R., Walenz B., Shatkay H., Dew I., Miller J.R., Flanigan M.J.,
RA   Edwards N.J., Bolanos R., Fasulo D., Halldorsson B.V., Hannenhalli S.,
RA   Turner R., Yooseph S., Lu F., Nusskern D.R., Shue B.C., Zheng X.H.,
RA   Zhong F., Delcher A.L., Huson D.H., Kravitz S.A., Mouchard L., Reinert K.,
RA   Remington K.A., Clark A.G., Waterman M.S., Eichler E.E., Adams M.D.,
RA   Hunkapiller M.W., Myers E.W., Venter J.C.;
RL   Submitted (SEP-2005) to the EMBL/GenBank/DDBJ databases.
RN   [8]
RP   NUCLEOTIDE SEQUENCE [LARGE SCALE MRNA].
RX   PubMed=15489334; DOI=10.1101/gr.2596504;
RG   The MGC Project Team;
RT   "The status, quality, and expansion of the NIH full-length cDNA project:
RT   the Mammalian Gene Collection (MGC).";
RL   Genome Res. 14:2121-2127(2004).
RN   [9]
RP   NUCLEOTIDE SEQUENCE [GENOMIC DNA] OF 30-144, POLYMORPHISM, AND VARIANT
RP   BLOOD GROUP SC5 LYS-47.
RX   PubMed=15660834; DOI=10.1111/j.1537-2995.2004.04226.x;
RA   Hue-Roye K., Chaudhuri A., Velliquette R.W., Fetics S., Thomas R., Balk M.,
RA   Wagner F.F., Flegel W.A., Reid M.E.;
RT   "STAR: a novel high-prevalence antigen in the Scianna blood group system.";
RL   Transfusion 45:245-247(2005).
RN   [10]
RP   POLYMORPHISM, AND VARIANTS BLOOD GROUP SC7 SER-35 AND SC6 GLN-81.
RX   PubMed=16371048; DOI=10.1111/j.1537-2995.2005.00646.x;
RA   Flegel W.A., Chen Q., Reid M.E., Martin J., Orsini L.A., Poole J.,
RA   Moulds M.K., Wagner F.F.;
RT   "SCER and SCAN: two novel high-prevalence antigens in the Scianna blood
RT   group system.";
RL   Transfusion 45:1940-1944(2005).
RN   [11]
RP   IDENTIFICATION BY MASS SPECTROMETRY [LARGE SCALE ANALYSIS].
RC   TISSUE=Liver;
RX   PubMed=24275569; DOI=10.1016/j.jprot.2013.11.014;
RA   Bian Y., Song C., Cheng K., Dong M., Wang F., Huang J., Sun D., Wang L.,
RA   Ye M., Zou H.;
RT   "An enzyme assisted RP-RPLC approach for in-depth analysis of human liver
RT   phosphoproteome.";
RL   J. Proteomics 96:253-262(2014).
CC   -!- FUNCTION: Possible role as a cell-adhesion or receptor molecule of
CC       erythroid cells.
CC   -!- INTERACTION:
CC       Q96PL5; P50402: EMD; NbExp=3; IntAct=EBI-13361852, EBI-489887;
CC       Q96PL5; Q9BYR6: KRTAP3-3; NbExp=3; IntAct=EBI-13361852, EBI-3957694;
CC       Q96PL5; Q68G75: LEMD1; NbExp=3; IntAct=EBI-13361852, EBI-12268900;
CC       Q96PL5; Q9Y6G1: TMEM14A; NbExp=3; IntAct=EBI-13361852, EBI-2800360;
CC   -!- SUBCELLULAR LOCATION: Cell membrane {ECO:0000269|PubMed:11783959};
CC       Single-pass type I membrane protein {ECO:0000255}. Cytoplasm
CC       {ECO:0000269|PubMed:11783959}.
CC   -!- TISSUE SPECIFICITY: Expressed in erythroid-enriched bone marrow (at
CC       protein level). Highly expressed in bone marrow and to a lower extent
CC       in leukocytes, thymus, lymph node and spleen.
CC       {ECO:0000269|PubMed:11549310, ECO:0000269|PubMed:11783959}.
CC   -!- DEVELOPMENTAL STAGE: Expressed in fetal liver blood cells (at protein
CC       level). Highly expressed in fetal liver. {ECO:0000269|PubMed:11549310,
CC       ECO:0000269|PubMed:11783959}.
CC   -!- PTM: Glycosylated.
CC   -!- POLYMORPHISM: ERMAP is responsible for the Scianna/Radin blood group
CC       system which comprises seven different antigens (PubMed:12393480). The
CC       Sc1 and Sc2 antigens are resulting from a single variation in position
CC       57; Arg-57 corresponds to the Sc2 antigen and Gly-57 to the Sc1
CC       antigen. The Sc2 antigen is rare with an occurrence of less than 1% in
CC       the population while Sc1 is more frequent. Sc3 is not expressed by
CC       individuals homozygous for a null allele encoding a truncated protein
CC       lacking its extracellular part (Sc-3). The Sc4 antigen corresponding to
CC       the previously defined Radin blood group antigen (Rd) is due to a
CC       single variation in position 60; Ala-60 corresponds to Sc4/Rd(+), the
CC       antigenic form of the protein. Sc4 is found in less than 1% of the
CC       population. Sc5/STAR, Sc6/SCER and Sc7/SCAN antigens are due to single
CC       variations in positions 47, 81 and 35 respectively. Alloantibodies to
CC       the low frequency Sc2 and Sc4 antigens are the cause of hemolytic
CC       disease in the newborn (PubMed:15660834, PubMed:16371048).
CC       {ECO:0000269|PubMed:12393480, ECO:0000269|PubMed:15660834,
CC       ECO:0000269|PubMed:16371048}.
CC   -!- SIMILARITY: Belongs to the immunoglobulin superfamily. BTN/MOG family.
CC       {ECO:0000305}.
CC   -!- WEB RESOURCE: Name=dbRBC/BGMUT; Note=Blood group antigen gene mutation
CC       database;
CC       URL="https://www.ncbi.nlm.nih.gov/gv/mhc/xslcgi.cgi?cmd=bgmut/systems_info&system=scianna";
CC   -!- WEB RESOURCE: Name=SeattleSNPs;
CC       URL="http://pga.gs.washington.edu/data/ermap/";
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DR   EMBL; AY049028; AAL11456.1; -; mRNA.
DR   EMBL; AF311284; AAL08411.1; -; mRNA.
DR   EMBL; AF311285; AAL08412.1; -; mRNA.
DR   EMBL; AJ505028; CAD43739.1; -; Genomic_DNA.
DR   EMBL; AJ505036; CAD43740.1; -; Genomic_DNA.
DR   EMBL; AJ505037; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505038; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505039; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505040; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505041; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505042; CAD43740.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505044; CAD43741.1; -; Genomic_DNA.
DR   EMBL; AJ505045; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505046; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505047; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505048; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505049; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; AJ505050; CAD43741.1; JOINED; Genomic_DNA.
DR   EMBL; BX537371; CAD97613.2; -; mRNA.
DR   EMBL; DQ090843; AAY88736.1; -; Genomic_DNA.
DR   EMBL; AL512353; -; NOT_ANNOTATED_CDS; Genomic_DNA.
DR   EMBL; CH471059; EAX07130.1; -; Genomic_DNA.
DR   EMBL; CH471059; EAX07133.1; -; Genomic_DNA.
DR   EMBL; BC099703; AAH99703.1; -; mRNA.
DR   EMBL; BC099707; AAH99707.1; -; mRNA.
DR   EMBL; BC099712; AAH99712.1; -; mRNA.
DR   EMBL; BC099713; AAH99713.1; -; mRNA.
DR   EMBL; AY644424; AAT66409.1; -; Genomic_DNA.
DR   CCDS; CCDS475.1; -.
DR   RefSeq; NP_001017922.1; NM_001017922.1.
DR   RefSeq; NP_061008.2; NM_018538.3.
DR   RefSeq; XP_006710376.1; XM_006710313.3.
DR   RefSeq; XP_011538872.1; XM_011540570.2.
DR   AlphaFoldDB; Q96PL5; -.
DR   SMR; Q96PL5; -.
DR   BioGRID; 125328; 27.
DR   IntAct; Q96PL5; 18.
DR   STRING; 9606.ENSP00000361595; -.
DR   GlyGen; Q96PL5; 1 site.
DR   iPTMnet; Q96PL5; -.
DR   PhosphoSitePlus; Q96PL5; -.
DR   BioMuta; ERMAP; -.
DR   DMDM; 74761033; -.
DR   EPD; Q96PL5; -.
DR   jPOST; Q96PL5; -.
DR   MassIVE; Q96PL5; -.
DR   MaxQB; Q96PL5; -.
DR   PaxDb; Q96PL5; -.
DR   PeptideAtlas; Q96PL5; -.
DR   PRIDE; Q96PL5; -.
DR   ProteomicsDB; 77708; -.
DR   Antibodypedia; 18175; 324 antibodies from 28 providers.
DR   DNASU; 114625; -.
DR   Ensembl; ENST00000372514.7; ENSP00000361592.3; ENSG00000164010.15.
DR   Ensembl; ENST00000372517.8; ENSP00000361595.2; ENSG00000164010.15.
DR   GeneID; 114625; -.
DR   KEGG; hsa:114625; -.
DR   MANE-Select; ENST00000372517.8; ENSP00000361595.2; NM_001017922.2; NP_001017922.1.
DR   UCSC; uc001cic.2; human.
DR   CTD; 114625; -.
DR   DisGeNET; 114625; -.
DR   GeneCards; ERMAP; -.
DR   HGNC; HGNC:15743; ERMAP.
DR   HPA; ENSG00000164010; Low tissue specificity.
DR   MalaCards; ERMAP; -.
DR   MIM; 111620; phenotype.
DR   MIM; 111750; phenotype.
DR   MIM; 609017; gene.
DR   neXtProt; NX_Q96PL5; -.
DR   OpenTargets; ENSG00000164010; -.
DR   PharmGKB; PA27860; -.
DR   VEuPathDB; HostDB:ENSG00000164010; -.
DR   eggNOG; KOG2177; Eukaryota.
DR   GeneTree; ENSGT00940000160531; -.
DR   InParanoid; Q96PL5; -.
DR   OMA; QVMEVEN; -.
DR   OrthoDB; 522383at2759; -.
DR   PhylomeDB; Q96PL5; -.
DR   TreeFam; TF317532; -.
DR   PathwayCommons; Q96PL5; -.
DR   SignaLink; Q96PL5; -.
DR   SIGNOR; Q96PL5; -.
DR   BioGRID-ORCS; 114625; 12 hits in 1075 CRISPR screens.
DR   ChiTaRS; ERMAP; human.
DR   GeneWiki; ERMAP; -.
DR   GenomeRNAi; 114625; -.
DR   Pharos; Q96PL5; Tbio.
DR   PRO; PR:Q96PL5; -.
DR   Proteomes; UP000005640; Chromosome 1.
DR   RNAct; Q96PL5; protein.
DR   Bgee; ENSG00000164010; Expressed in monocyte and 123 other tissues.
DR   ExpressionAtlas; Q96PL5; baseline and differential.
DR   Genevisible; Q96PL5; HS.
DR   GO; GO:0005829; C:cytosol; IDA:HPA.
DR   GO; GO:0009897; C:external side of plasma membrane; IBA:GO_Central.
DR   GO; GO:0005794; C:Golgi apparatus; IDA:HPA.
DR   GO; GO:0016021; C:integral component of membrane; IEA:UniProtKB-KW.
DR   GO; GO:0005886; C:plasma membrane; IDA:MGI.
DR   GO; GO:0005102; F:signaling receptor binding; IBA:GO_Central.
DR   GO; GO:0001817; P:regulation of cytokine production; IBA:GO_Central.
DR   GO; GO:0050852; P:T cell receptor signaling pathway; IBA:GO_Central.
DR   Gene3D; 2.60.120.920; -; 1.
DR   Gene3D; 2.60.40.10; -; 1.
DR   InterPro; IPR001870; B30.2/SPRY.
DR   InterPro; IPR043136; B30.2/SPRY_sf.
DR   InterPro; IPR003879; Butyrophylin_SPRY.
DR   InterPro; IPR013320; ConA-like_dom_sf.
DR   InterPro; IPR007110; Ig-like_dom.
DR   InterPro; IPR036179; Ig-like_dom_sf.
DR   InterPro; IPR013783; Ig-like_fold.
DR   InterPro; IPR003599; Ig_sub.
DR   InterPro; IPR013106; Ig_V-set.
DR   InterPro; IPR006574; PRY.
DR   InterPro; IPR003877; SPRY_dom.
DR   Pfam; PF13765; PRY; 1.
DR   Pfam; PF00622; SPRY; 1.
DR   Pfam; PF07686; V-set; 1.
DR   PRINTS; PR01407; BUTYPHLNCDUF.
DR   SMART; SM00409; IG; 1.
DR   SMART; SM00406; IGv; 1.
DR   SMART; SM00589; PRY; 1.
DR   SMART; SM00449; SPRY; 1.
DR   SUPFAM; SSF48726; SSF48726; 1.
DR   SUPFAM; SSF49899; SSF49899; 1.
DR   PROSITE; PS50188; B302_SPRY; 1.
DR   PROSITE; PS50835; IG_LIKE; 1.
PE   1: Evidence at protein level;
KW   Blood group antigen; Cell membrane; Cytoplasm; Disulfide bond;
KW   Glycoprotein; Immunoglobulin domain; Membrane; Phosphoprotein;
KW   Reference proteome; Signal; Transmembrane; Transmembrane helix.
FT   SIGNAL          1..29
FT                   /evidence="ECO:0000255"
FT   CHAIN           30..475
FT                   /note="Erythroid membrane-associated protein"
FT                   /id="PRO_0000226088"
FT   TOPO_DOM        30..155
FT                   /note="Extracellular"
FT                   /evidence="ECO:0000255"
FT   TRANSMEM        156..176
FT                   /note="Helical"
FT                   /evidence="ECO:0000255"
FT   TOPO_DOM        177..475
FT                   /note="Cytoplasmic"
FT                   /evidence="ECO:0000255"
FT   DOMAIN          30..140
FT                   /note="Ig-like V-type"
FT   DOMAIN          220..418
FT                   /note="B30.2/SPRY"
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00548"
FT   MOD_RES         418
FT                   /note="Phosphoserine"
FT                   /evidence="ECO:0000250|UniProtKB:Q9JLN5"
FT   CARBOHYD        132
FT                   /note="N-linked (GlcNAc...) asparagine"
FT                   /evidence="ECO:0000255"
FT   DISULFID        50..126
FT                   /evidence="ECO:0000255|PROSITE-ProRule:PRU00114"
FT   VARIANT         4
FT                   /note="A -> V (in dbSNP:rs35757049)"
FT                   /evidence="ECO:0000269|Ref.5"
FT                   /id="VAR_025478"
FT   VARIANT         26
FT                   /note="H -> Y (in dbSNP:rs33953680)"
FT                   /evidence="ECO:0000269|PubMed:12393480, ECO:0000269|Ref.5"
FT                   /id="VAR_025479"
FT   VARIANT         35
FT                   /note="G -> S (in Sc7 antigen; dbSNP:rs146429994)"
FT                   /evidence="ECO:0000269|PubMed:16371048"
FT                   /id="VAR_025480"
FT   VARIANT         47
FT                   /note="E -> K (in Sc5 antigen; dbSNP:rs56047316)"
FT                   /evidence="ECO:0000269|PubMed:15660834"
FT                   /id="VAR_025481"
FT   VARIANT         57
FT                   /note="G -> R (in Sc2 antigen; dbSNP:rs56025238)"
FT                   /evidence="ECO:0000269|PubMed:12393480"
FT                   /id="VAR_025482"
FT   VARIANT         60
FT                   /note="P -> A (in Sc4 antigen; dbSNP:rs56136737)"
FT                   /evidence="ECO:0000269|PubMed:12393480"
FT                   /id="VAR_025483"
FT   VARIANT         81
FT                   /note="R -> Q (in Sc6 antigen; dbSNP:rs368064875)"
FT                   /evidence="ECO:0000269|PubMed:16371048"
FT                   /id="VAR_025484"
FT   VARIANT         103..113
FT                   /note="DAQEGSVTLQI -> CPRGKCHSADP (in Sc-3 allele)"
FT                   /id="VAR_025485"
FT   VARIANT         114..475
FT                   /note="Missing (in Sc-3 allele)"
FT                   /id="VAR_025486"
FT   VARIANT         259
FT                   /note="C -> R (in dbSNP:rs35147822)"
FT                   /evidence="ECO:0000269|Ref.5"
FT                   /id="VAR_025487"
FT   VARIANT         263
FT                   /note="G -> E (in dbSNP:rs34441268)"
FT                   /evidence="ECO:0000269|Ref.5"
FT                   /id="VAR_025488"
FT   CONFLICT        452
FT                   /note="L -> P (in Ref. 4; CAD97613)"
FT                   /evidence="ECO:0000305"
SQ   SEQUENCE   475 AA;  52605 MW;  D796B0951EA02E0F CRC64;
     MEMASSAGSW LSGCLIPLVF LRLSVHVSGH AGDAGKFHVA LLGGTAELLC PLSLWPGTVP
     KEVRWLRSPF PQRSQAVHIF RDGKDQDEDL MPEYKGRTVL VRDAQEGSVT LQILDVRLED
     QGSYRCLIQV GNLSKEDTVI LQVAAPSVGS LSPSAVALAV ILPVLVLLIM VCLCLIWKQR
     RAKEKLLYEH VTEVDNLLSD HAKEKGKLHK AVKKLRSELK LKRAAANSGW RRARLHFVAV
     TLDPDTAHPK LILSEDQRCV RLGDRRQPVP DNPQRFDFVV SILGSEYFTT GCHYWEVYVG
     DKTKWILGVC SESVSRKGKV TASPANGHWL LRQSRGNEYE ALTSPQTSFR LKEPPRCVGI
     FLDYEAGVIS FYNVTNKSHI FTFTHNFSGP LRPFFEPCLH DGGKNTAPLV ICSELHKSEE
     SIVPRPEGKG HANGDVSLKV NSSLLPPKAP ELKDIILSLP PDLGPALQEL KAPSF
 
 
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