Homo sapiens (human): 57190
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Entry
57190 CDS
T01001
Symbol
SELENON, CFTD, CMYO3, CMYP3, MDRS1, RSMD1, RSS, SELN, SEPN1
Name
(RefSeq) selenoprotein N
KO
K19874
selenoprotein N
Organism
hsa
Homo sapiens (human)
Disease
H00701
Congenital fiber type disproportion
H01310
Multi-minicore disease
H01810
Congenital myopathy
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09180 Brite Hierarchies
09182 Protein families: genetic information processing
04131 Membrane trafficking [BR:
hsa04131
]
57190 (SELENON)
Membrane trafficking [BR:
hsa04131
]
Endoplasmic reticulum (ER) - Golgi transport
Others
Others
57190 (SELENON)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
EF-hand_6
EF-hand_1
EF-hand_7
EF-hand_5
Motif
Other DBs
NCBI-GeneID:
57190
NCBI-ProteinID:
NP_065184
OMIM:
606210
HGNC:
15999
Ensembl:
ENSG00000162430
UniProt:
Q9NZV5
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All DBs
Position
1:25800193..25818221
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AA seq
590 aa
AA seq
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MGRARPGQRGPPSPGPAAQPPAPPRRRARSLALLGALLAAAAAAAVRVCARHAEAQAAAR
QELALKTLGTDGLFLFSSLDTDGDMYISPEEFKPIAEKLTGSCSVTQTGVQWCSHSSLQP
QLPWLNUSSCLSLLRSTPAASCEEEELPPDPSEETLTIEARFQPLLPETMTKSKDGFLGV
SRLALSGLRNWTAAASPSAVFATRHFQPFLPPPGQELGEPWWIIPSELSMFTGYLSNNRF
YPPPPKGKEVIIHRLLSMFHPRPFVKTRFAPQGAVACLTAISDFYYTVMFRIHAEFQLSE
PPDFPFWFSPAQFTGHIILSKDATHVRDFRLFVPNHRSLNVDMEWLYGASESSNMEVDIG
YIPQMELEATGPSVPSVILDEDGSMIDSHLPSGEPLQFVFEEIKWQQELSWEEAARRLEV
AMYPFKKVSYLPFTEAFDRAKAENKLVHSILLWGALDDQSCUGSGRTLRETVLESSPILT
LLNESFISTWSLVKELEELQNNQENSSHQKLAGLHLEKYSFPVEMMICLPNGTVVHHINA
NYFLDITSVKPEEIESNLFSFSSTFEDPSTATYMQFLKEGLRRGLPLLQP
NT seq
1773 nt
NT seq
+upstream
nt +downstream
nt
atgggccgggcccggccgggccaacgcgggccgcccagccccggccccgccgcgcagcct
cccgcgccaccgcgccgccgcgcccgttccctggcgctgctcggagccctgctggccgcc
gccgctgccgccgccgtccgggtctgcgcccgccacgccgaggcccaggcggccgcgcgg
caggaactggcgctgaagaccctggggacagatggcctttttctcttttcctccttggac
actgacggggatatgtacatcagccctgaggagttcaaacccattgctgagaagctaaca
gggtcttgttctgtcacccagactggagtgcagtggtgcagtcacagctcactgcagcct
caacttccctggctcaattgatcctcctgcctcagcctcctgaggtcaactcccgcggcc
agctgcgaggaggaggagttgccccctgaccctagcgaggagacgctcaccatagaagcc
cgattccagcctctgctcccggagaccatgaccaagagcaaagatggcttcctaggggtc
tcccgcctcgccctgtccggcctccgaaactggacagccgccgcctcaccaagtgcagtg
tttgccacccgccacttccagcccttccttcccccgccaggccaggagctgggtgagccc
tggtggatcatccccagtgagctgagcatgttcactggctacctgtccaacaaccgcttc
tatccaccgccgcccaagggcaaggaggtcatcatccaccggctcctgagcatgttccac
cctcggccctttgtgaagacccgctttgcccctcagggagctgtggcctgcctgactgcc
atcagcgacttctactacactgtgatgttccggatccatgccgagttccagctcagtgag
ccgcccgacttccccttttggttctcccctgctcagttcaccggccacatcatcctctcc
aaagacgccacccacgtccgcgacttccggctcttcgtgcccaaccacaggtctctgaat
gtggacatggagtggctttacggggccagtgaaagcagcaacatggaggtggacatcggc
tacataccccagatggagctggaggccacgggcccctctgtgccctccgtgatcctggat
gaggatggcagcatgatcgacagccacctgccttcaggggagcccctgcagtttgtgttt
gaggagatcaagtggcagcaggagctgagctgggaggaggctgcccggcgcctggaggtg
gccatgtaccccttcaagaaggtctcctacttgccgttcactgaggccttcgaccgagcc
aaggctgagaacaagctggtgcactcaatcctgctgtggggggccctggatgaccagtcc
tgctgaggttcagggcggactctccgggagactgtcctggaaagttcgcccatcctcacc
ctgctcaacgagagcttcatcagcacctggtccctggtgaaggagctggaggaactgcag
aacaaccaggagaactcgtcccaccagaagctggctggcctgcacctggagaagtacagc
ttccccgtggagatgatgatctgcctgcccaatggcaccgtggtccatcacatcaatgcc
aactacttcttggacatcacctccgtgaagcccgaggaaatcgagagcaatctcttcagc
ttctcatccacctttgaagacccgtccacggccacctacatgcagttcctgaaggaggga
ctccggcgtggcctgcccctcctccagccctag
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