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EBIDatabasesDatabase BrowsingDbfetch

EBI Dbfetch

ID   AAC21457; SV 1; linear; genomic DNA; STD; HUM; 1770 BP.
XX
PA   AF048704.1
XX
DE   Homo sapiens (human) lamin B receptor homolog TM7SF2
XX
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;
XX
FH   Key             Location/Qualifiers
FH
FT   source          1..1770
FT                   /organism="Homo sapiens"
FT                   /chromosome="11"
FT                   /map="11q13"
FT                   /mol_type="genomic DNA"
FT   CDS             join(AF048704.1:255..960,AF048704.1:1315..1509,
FT                   AF048704.1:1586..1689,AF048704.1:2830..2949,
FT                   AF048704.1:3036..3204,AF048704.1:3437..3517,
FT                   AF048704.1:3599..3721,AF048704.1:4017..4288)
FT                   /codon_start=1
FT                   /product="lamin B receptor homolog TM7SF2"
FT                   /note="ANG1"
FT                   /db_xref="GDB:9466549"
FT                   /db_xref="GOA:O76062"
FT                   /db_xref="HGNC:11863"
FT                   /db_xref="InterPro:IPR001171"
FT                   /db_xref="UniProtKB/Swiss-Prot:O76062"
FT                   /func_characterised="similar sequence"
FT                   /protein_id="AAC21457.1"
FT                   /translation="MEGFGGVGGRGTRGFAAKGVWRGRAEEGPVLGAAERGFMVSTGSR
FT                   RRVFEGPGGGGLRWTPGKGTGRQRGAWGPRAEDGVRRRTLGMPRGSRRDVRAPCGPAGS
FT                   WGARGGRRRDGPSRRRRGSATAAARHHVPPAPGGPFGPRAPAGSTRVPARAGGAVEPTG
FT                   AAAVARLARPAGGALPTAGAQGAGPARGRSGEGSEWARRGKGRPGPYQSPLGPAVAEGQ
FT                   ELKDKSRLRYPINGFQALVLTALLVGLGMSAGLPLGALPEMLLPLAFVATLTAFIFSLF
FT                   LYMKAQVAPVSALAPGGNSGNPIYDFFLGRELNPRICFFDFKYFCELRPGLIGWVLINL
FT                   ALLMKEAELRGSPSLAMWLVNGFQLLYVGDALWHEEAVLTTMDITHDGFGFMLAFGDMA
FT                   WVPFTYSLQAQFLLHHPQPLGLPMASVICLINATGYYIFRGANSQKNTFRKNPSDPRVA
FT                   GLETISTATGRKLLVSGWWGMVRHPNYLGDLIMALAWSLPCGVSHLLPYFYLLYFTALL
FT                   VHREARDERSACRSTAWPGRSTAGVCLTASCPTSTEAAPPPQVGHVPTHPPAHPGPGAS
FT                   THLGLKGLHPTQP"
XX
SQ   Sequence 1770 BP; 279 A; 541 C; 601 G; 349 T; 0 other; 2207529536 CRC32;
     atggaaggct ttgggggtgt cggaggcaga gggacccggg ggtttgcagc gaagggtgtc        60
     tggagaggga gagctgagga ggggccggtt ctgggggctg cagaacgggg atttatggtg       120
     tcgactggga gcaggaggag ggtcttcgag gggcctgggg gcgggggact aagatggacg       180
     cctgggaagg gaactgggag gcagcggggt gcctgggggc cgagggctga ggacggggtg       240
     cggaggcgca ctctgggaat gccgagaggg tcccgcagag acgtcagggc gccgtgcggg       300
     ccggcgggga gctggggggc taggggcgga cgccgacgtg atggcccttc ccgcaggcgc       360
     cgcggctctg ctactgctgc tgcccgccac catgttccac ctgctcctgg cggcccgttc       420
     gggccccgcg cgcctgctgg gtccacccgc gtccctgccc gggctggagg tgctgtggag       480
     cccacgggcg ctgctgctgt ggctcgcctg gctcggcctg caggcggcgc tctacctact       540
     gccggcgcgc aaggtgcggg ccccgctcgc ggacgctcgg gggagggaag cgaatgggct       600
     cggcgaggga aaggacgccc cgggccttat cagagccccc ttggacccgc agtggccgag       660
     gggcaggaat tgaaggacaa gagtcgcctg cgctatccta ttaacggctt ccaggccctg       720
     gtgctgacag ccctgttggt ggggctgggg atgtcagcgg ggctgcctct gggggcgctc       780
     ccggaaatgc tcctgccctt ggcgtttgtc gccaccctca ccgctttcat cttcagcctc       840
     tttctctaca tgaaggcgca ggtagcccca gtttcggccc tggcacctgg ggggaactca       900
     ggcaatccga tttacgactt ttttctggga cgagagctca accctcgtat ctgtttcttc       960
     gacttcaaat atttctgtga actgcgaccc ggcctcatcg gctgggtcct catcaacctg      1020
     gccctgttga tgaaggaggc agagcttcga ggcagtccct cactggccat gtggctggtc      1080
     aatggcttcc agttgctcta cgtgggtgat gccctctggc acgaggaggc cgtcctcacc      1140
     accatggata tcacacatga cgggtttggc ttcatgctgg cgtttgggga catggcctgg      1200
     gtgcccttca cctacagcct gcaggcccag ttcctgctgc accacccgca gcccctgggg      1260
     ttgcccatgg cctctgtcat ctgcctcatc aatgctactg gttactacat cttccgtggg      1320
     gcgaattccc agaaaaacac tttccgaaag aatccttctg accccagagt ggctgggctt      1380
     gagaccatct ctacagccac agggcggaaa ctgctggtgt ctgggtggtg gggtatggtc      1440
     cgccatccca actatcttgg agacctcatc atggctctgg cttggtcctt gccctgcggg      1500
     gtgtcacacc tgctgcccta cttctacctc ctctacttca ccgcgctgct ggtgcaccgt      1560
     gaggcccggg atgagcggag tgcctgcaga agtacggcct ggcctggcag gagtactgcc      1620
     ggcgtgtgcc ttaccgcatc atgccctaca tctactgaag cggctccacc accccaggtg      1680
     gggcatgtgc ccactcatcc accagcacac ccaggaccag gagcctcgac acacttggga      1740
     ctcaagggct tgcaccccac ccagccctga                                       1770
//
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