Dbfetch
ID FJ198229.1:1212..1484:rRNA; SV 1; linear; genomic DNA; STD; HUM; 273 BP. XX PA FJ198229.1 XX DT 24-DEC-2008 (Rel. 98, Created) DT 24-DEC-2008 (Rel. 98, Last updated, Version 1) XX DE Homo sapiens (human) partial 12S ribosomal RNA XX KW . XX OS Homo sapiens (human) OC Eukaryota; Metazoa; Chordata; Craniata; Vertebrata; Euteleostomi; Mammalia; OC Eutheria; Euarchontoglires; Primates; Haplorrhini; Catarrhini; Hominidae; OC Homo. OG Mitochondrion XX RN [1] RX DOI; 10.1016/j.ajhg.2008.11.002. RX PUBMED; 19026397. RA Ji Y., Zhang A.M., Jia X., Zhang Y.P., Xiao X., Li S., Guo X., RA Bandelt H.J., Zhang Q., Yao Y.G.; RT "Mitochondrial DNA haplogroups M7b1'2 and M8a affect clinical expression of RT leber hereditary optic neuropathy in Chinese families with the m.11778G-->a RT mutation"; RL Am. J. Hum. Genet. 83(6):760-768(2008). XX RN [2] RA Zhang A.-M., Yao Y.-G.; RT ; RL Submitted (08-SEP-2008) to the INSDC. RL Key Laboratory of Animal Models and Human Disease Mechanisms, Kunming RL Institute of Zoology, Chinese Academy of Sciences, 32 Jiaochang Donglu, RL Kunming, Yunnan 650223, China XX DR MD5; 061e3690d52a95f606d0f4bf683d1202. XX FH Key Location/Qualifiers FH FT source 1..273 FT /organism="Homo sapiens" FT /organelle="mitochondrion" FT /isolate="LHON family Le1053" FT /mol_type="genomic DNA" FT /db_xref="taxon:9606" FT rRNA FJ198229.1:1212..>1484 FT /product="12S ribosomal RNA" XX SQ Sequence 273 BP; 85 A; 78 C; 51 G; 59 T; 0 other; aataggtttg gtcctggcct ttctattagc tcttagtaag attacacatg caagcatccc 60 cgttccagtg agttcaccct ctaaatcacc acgatcaaaa gggacaagca tcaagcacgc 120 agcaatgcag ctcaaaacgc ttagcctagc cacaccccca cgggaaacag cagtgattaa 180 cctttagcaa taaacgaaag tttaactaag ctatactaac cccagggttg gtcaatttcg 240 tgccagccac cgcggtcaca cgattaaccc aag 273 //