Homo sapiens (human): 866
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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)
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GFIT
Motif
Pfam:
Serpin
Motif
Other DBs
NCBI-GeneID:
866
NCBI-ProteinID:
NP_001747
OMIM:
122500
HGNC:
1540
Ensembl:
ENSG00000170099
UniProt:
P08185
A0A2Z4LCH4
Structure
PDB
PDBj
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All DBs
Position
14:complement(94304248..94323336)
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AA seq
405 aa
AA seq
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MPLLLYTCLLWLPTSGLWTVQAMDPNAAYVNMSNHHRGLASANVDFAFSLYKHLVALSPK
KNIFISPVSISMALAMLSLGTCGHTRAQLLQGLGFNLTERSETEIHQGFQHLHQLFAKSD
TSLEMTMGNALFLDGSLELLESFSADIKHYYESEVLAMNFQDWATASRQINSYVKNKTQG
KIVDLFSGLDSPAILVLVNYIFFKGTWTQPFDLASTREENFYVDETTVVKVPMMLQSSTI
SYLHDSELPCQLVQMNYVGNGTVFFILPDKGKMNTVIAALSRDTINRWSAGLTSSQVDLY
IPKVTISGVYDLGDVLEEMGIADLFTNQANFSRITQDAQLKSSKVVHKAVLQLNEEGVDT
AGSTGVTLNLTSKPIILRFNQPFIIMIFDHFTWSSLFLARVMNPV
NT seq
1218 nt
NT seq
+upstream
nt +downstream
nt
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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