ID M21569; SV 1; linear; genomic DNA; STD; HUM; 882 BP. XX AC M21569; XX DT 22-APR-1989 (Rel. 19, Created) DT 14-NOV-2006 (Rel. 89, Last updated, Version 7) XX DE Homo sapiens transferrin (TF) gene, exon 2 and partial 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 1-882 RX DOI; 10.1016/0378-1119(86)90277-5. RX PUBMED; 3106157. RA Adrian G.S., Korinek B.W., Bowman B.H., Yang F.; RT "The human transferrin gene: 5' region contains conserved sequences which RT match the control elements regulated by heavy metals, glucocorticoids and RT acute phase reaction"; RL Gene 49(2):167-175(1986). XX DR MD5; 6899644e35e6eca353afc048e655abb3. DR Ensembl-Gn; ENSG00000091513; homo_sapiens. DR Ensembl-Tr; ENST00000402696; homo_sapiens. XX FH Key Location/Qualifiers FH FT source 1..882 FT /organism="Homo sapiens" FT /chromosome="3" FT /map="3q21" FT /mol_type="genomic DNA" FT /clone="J85TF1" FT /db_xref="taxon:9606" FT intron <1..317 FT /gene="TF" FT /number=1 FT /note="G00-120-432" FT mRNA join(M15673.1:<1130..1172,318..>490) FT /gene="TF" FT /product="transferrin" FT CDS join(M15673.1:1130..1172,318..>490) FT /codon_start=1 FT /gene="TF" FT /product="transferrin" FT /number=1 FT /db_xref="GOA:P02787" FT /db_xref="HGNC:HGNC:11740" FT /db_xref="InterPro:IPR001156" FT /db_xref="InterPro:IPR016357" FT /db_xref="InterPro:IPR018195" FT /db_xref="InterPro:IPR030685" FT /db_xref="PDB:1A8E" FT /db_xref="PDB:1A8F" FT /db_xref="PDB:1B3E" FT /db_xref="PDB:1BP5" FT /db_xref="PDB:1BTJ" FT /db_xref="PDB:1D3K" FT /db_xref="PDB:1D4N" FT /db_xref="PDB:1DTG" FT /db_xref="PDB:1FQE" FT /db_xref="PDB:1FQF" FT /db_xref="PDB:1JQF" FT /db_xref="PDB:1N7W" FT /db_xref="PDB:1N7X" FT /db_xref="PDB:1N84" FT /db_xref="PDB:1OQG" FT /db_xref="PDB:1OQH" FT /db_xref="PDB:1RYO" FT /db_xref="PDB:1SUV" FT /db_xref="PDB:2HAU" FT /db_xref="PDB:2HAV" FT /db_xref="PDB:2O7U" FT /db_xref="PDB:2O84" FT /db_xref="PDB:3FGS" FT /db_xref="PDB:3QYT" FT /db_xref="PDB:3S9L" FT /db_xref="PDB:3S9M" FT /db_xref="PDB:3S9N" FT /db_xref="PDB:3SKP" FT /db_xref="PDB:3V83" FT /db_xref="PDB:3V89" FT /db_xref="PDB:3V8X" FT /db_xref="PDB:3VE1" FT /db_xref="PDB:4H0W" FT /db_xref="PDB:4X1B" FT /db_xref="PDB:4X1D" FT /db_xref="PDB:5DYH" FT /db_xref="UniProtKB/Swiss-Prot:P02787" FT /protein_id="AAA61143.2" FT /translation="MRLAVGALLVCAVLGLCLAVPDKTVRWCAVSEHEATKCQSFRDHM FT KSVIPSDGPSVACVKKASYLDCIRAIA" FT exon 318..490 FT /gene="TF" FT /number=2 FT intron 491..>882 FT /gene="TF" FT /number=2 FT /note="G00-120-432" XX SQ Sequence 882 BP; 216 A; 196 C; 261 G; 208 T; 1 other; aggggccagg acagtgatgg gaggagacaa ggcggataca gaggagcaga ttgtcatctc 60 cagctgggag gtgatgccat gcctgcaccc tctggccagc agagggtggt cagtaggaaa 120 ctgggaggcc attagggcaa ccttctattg gctcagactc agaatgcagt agaacttgtg 180 ccctgtagtg ttcatggaca ggagtgagag gaggacagga ctgaggggat gtggctgtca 240 aggcctttct aggggcgatg ctgtctctcc ctcagcatag ggagtgggcc cttccacctc 300 tggcctctct cccccagggc tgtgtctggc tgtccctgat aaaactgtga gatggtgtgc 360 agtgtcggag catgaggcca ctaagtgcca gagtttccgc gaccatatga aaagcgtcat 420 tccatccgat ggtcccagtg ttgcttgtgt gaagaaagcc tcctaccttg attgcatcag 480 ggccattgcg gtaagtcgct gctgcctaaa agagagtgga agaaagccat actttctctg 540 tttccagtca ctttggaaca attctttact cacaggtagg aggctgatat atggggcagt 600 caaccttgac ttactaaaat cacttcaaaa gtggaaatgg ggaggttttc tttaangggt 660 ctggaaagca aaagtcaaaa agcacattaa cttttgcttt ccagacacag tagacgcaag 720 ggtgactgtt ttgagaccct aggttctctg aacttggcga aaatataaga atgcctgcta 780 tcaggctggg cgcggtggct catgctgaaa tcctagcact ttgggaggct gaggcaggtg 840 gatcacctga ggtcaggagt tcgagaccag cctggccaac at 882 //