ID AF196489; SV 1; linear; mRNA; STD; HUM; 1197 BP.
XX
AC AF196489;
XX
DT 12-JUL-2002 (Rel. 72, Created)
DT 07-OCT-2008 (Rel. 97, Last updated, Version 4)
XX
DE Homo sapiens MHC class I antigen (HLA-C) mRNA, HLA-C-Cw*0409 N allele,
DE complete cds.
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]
RP 1-1197
RX DOI; 10.1034/j.1399-0039.2002.590204.x.
RX PUBMED; 12028535.
RA Balas A., Santos S., Aviles M.J., Garcia-Sanchez F., Lillo R., Alvarez A.,
RA Villar-Guimerans L.M., Vicario J.L.;
RT "Elongation of the cytoplasmic domain, due to a point deletion at exon 7,
RT results in an HLA-C null allele, Cw*0409 N";
RL Tissue Antigens 59(2):95-100(2002).
XX
RN [2]
RP 1-1197
RA Santos S., Balas A., Vicario J.L.;
RT ;
RL Submitted (20-OCT-1999) to the INSDC.
RL Histocompatibility, Regional Transfusion Center from Madrid, Avda. Menendez
RL Pelayo 65, Madrid 28009, Spain
XX
DR MD5; 7193c0b1fa71f17bd952bb949fd76a30.
DR H-InvDB; HIT000073678_03.4.
DR H-InvDB; HIT000073678_04.4.
DR H-InvDB; HIT000073678_05.4.
DR IMGT/HLA; HLA-C*04:09N; HLA01451.
XX
FH Key Location/Qualifiers
FH
FT source 1..1197
FT /organism="Homo sapiens"
FT /chromosome="6"
FT /map="6p21"
FT /mol_type="mRNA"
FT /note="peripheral blood lymphocyte"
FT /db_xref="taxon:9606"
FT CDS 1..1197
FT /codon_start=1
FT /gene="HLA-C"
FT /product="MHC class I antigen"
FT /db_xref="GOA:Q95HN1"
FT /db_xref="H-InvDB:HIT000073678_02.4"
FT /db_xref="InterPro:IPR001039"
FT /db_xref="InterPro:IPR003006"
FT /db_xref="InterPro:IPR003597"
FT /db_xref="InterPro:IPR007110"
FT /db_xref="InterPro:IPR010579"
FT /db_xref="InterPro:IPR011161"
FT /db_xref="InterPro:IPR011162"
FT /db_xref="InterPro:IPR013783"
FT /db_xref="InterPro:IPR036179"
FT /db_xref="InterPro:IPR037055"
FT /db_xref="UniProtKB/TrEMBL:Q95HN1"
FT /protein_id="AAM76870.1"
FT /translation="MRVMAPRTLILLLSGALALTETWAGSHSMRYFSTSVSWPGRGEPR
FT FIAVGYVDDTQFVRFDSDAASPRGEPREPWVEQEGPEYWDRETQKYKRQAQADRVNLRK
FT LRGYYNQSEDGSHTLQRMFGCDLGPDGRLLRGYNQFAYDGKDYIALNEDLRSWTAADTA
FT AQITQRKWEAAREAEQRRAYLEGTCVEWLRRYLENGKETLQRAEHPKTHVTHHPVSDHE
FT ATLRCWALGFYPAEITLTWQWDGEDQTQDTELVETRPAGDGTFQKWAAVVVPSGEEQRY
FT TCHVQHEGLPEPLTLRWKPSSQPTIPIVGIVAGLAVLAVLAVLGAMVAVVMCRRKSSGG
FT KGGSCSQAASSNSAQGSDESLIACKPETAACVGLRCRISSHLSFVTSRASGISFCKGI"
XX
SQ Sequence 1197 BP; 236 A; 357 C; 398 G; 206 T; 0 other;
atgcgggtca tggcgccccg aaccctcatc ctgctgctct cgggagccct ggccctgacc 60
gagacctggg ccggctccca ctccatgagg tatttctcca catccgtgtc ctggcccggc 120
cgcggggagc cccgcttcat cgcagtgggc tacgtggacg acacgcagtt cgtgcggttc 180
gacagcgacg ccgcgagtcc aagaggggag ccgcgggagc cgtgggtgga gcaggagggg 240
ccggagtatt gggaccggga gacacagaag tacaagcgcc aggcacaggc tgaccgagtg 300
aacctgcgga aactgcgcgg ctactacaac cagagcgagg acgggtctca caccctccag 360
aggatgtttg gctgcgacct ggggccggac gggcgcctcc tccgcgggta taaccagttc 420
gcctacgacg gcaaggatta catcgccctg aacgaggatc tgcgctcctg gaccgccgcg 480
gacacggcgg ctcagatcac ccagcgcaag tgggaggcgg cccgtgaggc ggagcagcgg 540
agagcctacc tggagggcac gtgcgtggag tggctccgca gatacctgga gaacgggaag 600
gagacgctgc agcgcgcgga acacccaaag acacacgtga cccaccatcc cgtctctgac 660
catgaggcca ccctgaggtg ctgggccctg ggcttctacc ctgcggagat cacactgacc 720
tggcagtggg atggggagga ccaaactcag gacaccgagc ttgtggagac caggccagca 780
ggagatggaa ccttccagaa gtgggcagct gtggtggtgc cttctggaga agagcagaga 840
tacacgtgcc atgttcagca cgaggggctg ccggagcccc tcaccctgag atggaagccg 900
tcttcccagc ccaccatccc catcgtgggc atcgttgctg gcctggctgt cctggctgtc 960
ctagctgtcc taggagctat ggtggctgtt gtgatgtgta ggaggaagag ctcaggtgga 1020
aaaggaggga gctgctctca ggctgcgtcc agcaacagtg cccagggctc tgatgagtct 1080
ctcatcgctt gtaagcctga gacagctgcc tgtgtgggac tgagatgcag gatttcttca 1140
cacctctcct ttgtgacttc aagagcctct ggcatctctt tctgcaaagg catctga 1197
//