Homo sapiens (human): 10062
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Entry
10062 CDS
T01001
Symbol
NR1H3, LXR-a, LXRA, RLD-1
Name
(RefSeq) nuclear receptor subfamily 1 group H member 3
KO
K08536
liver X receptor alpha
Organism
hsa
Homo sapiens (human)
Pathway
hsa03320
PPAR signaling pathway
hsa04148
Efferocytosis
hsa04931
Insulin resistance
hsa04932
Non-alcoholic fatty liver disease
hsa05160
Hepatitis C
Network
nt06163
Hepatitis C virus (HCV)
nt06263
Hepatocellular carcinoma
nt06535
Efferocytosis
Element
N00530
HCV core to RXRA/LXRA-mediated transcription
N01781
Activation of LXRs by oxysterols
Drug target
Abequolixron (
DG03218
):
D12298
D12299
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09140 Cellular Processes
09141 Transport and catabolism
04148 Efferocytosis
10062 (NR1H3)
09150 Organismal Systems
09152 Endocrine system
03320 PPAR signaling pathway
10062 (NR1H3)
09160 Human Diseases
09172 Infectious disease: viral
05160 Hepatitis C
10062 (NR1H3)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
10062 (NR1H3)
04931 Insulin resistance
10062 (NR1H3)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
10062 (NR1H3)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
hsa03310
]
10062 (NR1H3)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
10062 (NR1H3)
Nuclear receptors [BR:
hsa03310
]
1. Thyroid hormone like
1H. Liver X receptor like receptor
10062 (NR1H3)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Hormone_recep
zf-C4
Motif
Other DBs
NCBI-GeneID:
10062
NCBI-ProteinID:
NP_005684
OMIM:
602423
HGNC:
7966
Ensembl:
ENSG00000025434
Pharos:
Q13133
(Tchem)
UniProt:
Q13133
B4DXU5
F1D8N1
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:47248300..47269033
Genome browser
AA seq
447 aa
AA seq
DB search
MSLWLGAPVPDIPPDSAVELWKPGAQDASSQAQGGSSCILREEARMPHSAGGTAGVGLEA
AEPTALLTRAEPPSEPTEIRPQKRKKGPAPKMLGNELCSVCGDKASGFHYNVLSCEGCKG
FFRRSVIKGAHYICHSGGHCPMDTYMRRKCQECRLRKCRQAGMREECVLSEEQIRLKKLK
RQEEEQAHATSLPPRASSPPQILPQLSPEQLGMIEKLVAAQQQCNRRSFSDRLRVTPWPM
APDPHSREARQQRFAHFTELAIVSVQEIVDFAKQLPGFLQLSREDQIALLKTSAIEVMLL
ETSRRYNPGSESITFLKDFSYNREDFAKAGLQVEFINPIFEFSRAMNELQLNDAEFALLI
AISIFSADRPNVQDQLQVERLQHTYVEALHAYVSIHHPHDRLMFPRMLMKLVSLRTLSSV
HSEQVFALRLQDKKLPPLLSEIWDVHE
NT seq
1344 nt
NT seq
+upstream
nt +downstream
nt
atgtccttgtggctgggggcccctgtgcctgacattcctcctgactctgcggtggagctg
tggaagccaggcgcacaggatgcaagcagccaggcccagggaggcagcagctgcatcctc
agagaggaagccaggatgccccactctgctgggggtactgcaggggtggggctggaggct
gcagagcccacagccctgctcaccagggcagagcccccttcagaacccacagagatccgt
ccacaaaagcggaaaaaggggccagcccccaaaatgctggggaacgagctatgcagcgtg
tgtggggacaaggcctcgggcttccactacaatgttctgagctgcgagggctgcaaggga
ttcttccgccgcagcgtcatcaagggagcgcactacatctgccacagtggcggccactgc
cccatggacacctacatgcgtcgcaagtgccaggagtgtcggcttcgcaaatgccgtcag
gctggcatgcgggaggagtgtgtcctgtcagaagaacagatccgcctgaagaaactgaag
cggcaagaggaggaacaggctcatgccacatccttgccccccagggcttcctcacccccc
caaatcctgccccagctcagcccggaacaactgggcatgatcgagaagctcgtcgctgcc
cagcaacagtgtaaccggcgctccttttctgaccggcttcgagtcacgccttggcccatg
gcaccagatccccatagccgggaggcccgtcagcagcgctttgcccacttcactgagctg
gccatcgtctctgtgcaggagatagttgactttgctaaacagctacccggcttcctgcag
ctcagccgggaggaccagattgccctgctgaagacctctgcgatcgaggtgatgcttctg
gagacatctcggaggtacaaccctgggagtgagagtatcaccttcctcaaggatttcagt
tataaccgggaagactttgccaaagcagggctgcaagtggaattcatcaaccccatcttc
gagttctccagggccatgaatgagctgcaactcaatgatgccgagtttgccttgctcatt
gctatcagcatcttctctgcagaccggcccaacgtgcaggaccagctccaggtagagagg
ctgcagcacacatatgtggaagccctgcatgcctacgtctccatccaccatccccatgac
cgactgatgttcccacggatgctaatgaaactggtgagcctccggaccctgagcagcgtc
cactcagagcaagtgtttgcactgcgtctgcaggacaaaaagctcccaccgctgctctct
gagatctgggatgtgcacgaatga
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