Homo sapiens (human): 866 Help Entry 866               CDS       T01001                                  Symbol SERPINA6, CBG Name (RefSeq) serpin family A member 6   KO K04525   serpin A Organism hsa  Homo sapiens (human) Network nt06019  Steroid hormone biosynthesis   Element N00313   Transport of cortisol Disease H01163   Corticosteroid-binding globulin (CBG) deficiency Brite KEGG Orthology (KO) [BR:hsa00001]  09180 Brite Hierarchies   09181 Protein families: metabolism    01002 Peptidases and inhibitors [BR:hsa01002]     866 (SERPINA6) Peptidases and inhibitors [BR:hsa01002]  Peptidase inhibitors   Family I4: serpin family    866 (SERPINA6) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Motif Pfam:  Serpin Motif Other DBs NCBI-GeneID:  866 NCBI-ProteinID:  NP_001747 OMIM:  122500 HGNC:  1540 Ensembl:  ENSG00000170099 UniProt:  P08185 A0A2Z4LCH4 Structure PDB LinkDB All DBs Position 14:complement(94304248..94323336) Genome browser AA seq 405 aa AA seqDB search MPLLLYTCLLWLPTSGLWTVQAMDPNAAYVNMSNHHRGLASANVDFAFSLYKHLVALSPK KNIFISPVSISMALAMLSLGTCGHTRAQLLQGLGFNLTERSETEIHQGFQHLHQLFAKSD TSLEMTMGNALFLDGSLELLESFSADIKHYYESEVLAMNFQDWATASRQINSYVKNKTQG KIVDLFSGLDSPAILVLVNYIFFKGTWTQPFDLASTREENFYVDETTVVKVPMMLQSSTI SYLHDSELPCQLVQMNYVGNGTVFFILPDKGKMNTVIAALSRDTINRWSAGLTSSQVDLY IPKVTISGVYDLGDVLEEMGIADLFTNQANFSRITQDAQLKSSKVVHKAVLQLNEEGVDT AGSTGVTLNLTSKPIILRFNQPFIIMIFDHFTWSSLFLARVMNPV NT seq 1218 nt NT seq  +upstreamnt  +downstreamnt atgccactcctcctgtacacctgtcttctctggctgcccaccagcggcctctggaccgtc caggccatggatcctaacgctgcttatgtgaacatgagtaaccatcaccggggcctggct tcagccaacgttgactttgccttcagcctgtataagcacctagtggccttgagtcccaaa aagaacattttcatctcccctgtgagcatctccatggccttagctatgctgtccctgggc acctgtggccacacacgggcccagcttctccagggcctgggtttcaacctcactgagagg tctgagactgagatccaccagggtttccagcacctgcaccaactctttgcaaagtcagac accagcttagaaatgaccatgggcaatgccttgtttcttgatggcagcctggagttgctg gagtcattctcagcagacatcaagcactactatgagtcagaggtcttggctatgaatttc caggactgggcaacagccagcagacagatcaacagctatgtcaagaataagacacagggg aaaattgtcgacttgttttcagggctggatagcccagccatcctcgtcctggtcaactat atcttcttcaaaggcacatggacacagccctttgacctggcaagcaccagggaggagaac ttctatgtggacgagacaactgtggtgaaggtgcccatgatgttgcagtcgagcaccatc agttaccttcatgactcggagctcccctgccagctggtgcagatgaactacgtgggcaat gggactgtcttcttcatccttccggacaaggggaagatgaacacagtcatcgctgcactg agccgggacacgattaacaggtggtccgcaggcctgaccagcagccaggtggacctgtac attccaaaggtcaccatctctggagtctatgacctcggagatgtgctggaggaaatgggc attgcagacttgttcaccaaccaggcaaatttctcacgcatcacccaggacgcccagctg aagtcatcaaaggtggtccataaagctgtgctgcaactcaatgaggagggtgtggacaca gctggctccactggggtcaccctaaacctgacgtccaagcctatcatcttgcgtttcaac cagcccttcatcatcatgatcttcgaccacttcacctggagcagccttttcctggcgagg gttatgaacccagtgtaa

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