Homo sapiens (human): 5468
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Entry
5468 CDS
T01001
Symbol
PPARG, CIMT1, GLM1, NR1C3, PPARG1, PPARG2, PPARG5, PPARgamma
Name
(RefSeq) peroxisome proliferator activated receptor gamma
KO
K08530
peroxisome proliferator-activated receptor gamma
Organism
hsa
Homo sapiens (human)
Pathway
hsa03320
PPAR signaling pathway
hsa04152
AMPK signaling pathway
hsa04211
Longevity regulating pathway
hsa04380
Osteoclast differentiation
hsa04714
Thermogenesis
hsa04932
Non-alcoholic fatty liver disease
hsa05016
Huntington disease
hsa05200
Pathways in cancer
hsa05202
Transcriptional misregulation in cancer
hsa05216
Thyroid cancer
hsa05417
Lipid and atherosclerosis
Network
nt06240
Transcription
nt06274
Thyroid cancer
Element
N00126
PAX8-PPARG fusion to PPARG-mediated transcription
N00138
EWSR1-NR4A3
Disease
H00032
Thyroid cancer
H00409
Type 2 diabetes mellitus
H00420
Familial partial lipodystrophy
H02106
Genetic obesity
Drug target
Aleglitazar:
D08845
Arhalofenate:
D09579
Bocidelpar (
DG03197
):
D12242
D12243
Carfloglitazar:
D12484
Ciglitazone:
D03493
Darglitazone sodium:
D03653
Edaglitazone sodium:
D03941
Englitazone sodium:
D03996
Farglitazar:
D04132
Halofenate:
D04411
Indeglitazar:
D09350
Leriglitazone (
DG03060
):
D11603
D11604
Lobeglitazone:
D11923
Mifobate:
D05030
Muraglitazar:
D05091
Netoglitazone:
D05150
Peliglitazar:
D05397
Pioglitazone (
DG00117
):
D00945
<JP/US>
D08378
Reglitazar:
D01971
Rivoglitazone:
D05739
Rosiglitazone (
DG00116
):
D00596
D08491
Seladelpar (
DG02957
):
D11256
D11257
Sodelglitazar:
D06647
Tesaglitazar:
D01274
Troglitazone:
D00395
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09130 Environmental Information Processing
09132 Signal transduction
04152 AMPK signaling pathway
5468 (PPARG)
09150 Organismal Systems
09152 Endocrine system
03320 PPAR signaling pathway
5468 (PPARG)
09158 Development and regeneration
04380 Osteoclast differentiation
5468 (PPARG)
09149 Aging
04211 Longevity regulating pathway
5468 (PPARG)
09159 Environmental adaptation
04714 Thermogenesis
5468 (PPARG)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
5468 (PPARG)
05202 Transcriptional misregulation in cancer
5468 (PPARG)
09162 Cancer: specific types
05216 Thyroid cancer
5468 (PPARG)
09164 Neurodegenerative disease
05016 Huntington disease
5468 (PPARG)
09166 Cardiovascular disease
05417 Lipid and atherosclerosis
5468 (PPARG)
09167 Endocrine and metabolic disease
04932 Non-alcoholic fatty liver disease
5468 (PPARG)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
5468 (PPARG)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
hsa03310
]
5468 (PPARG)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
5468 (PPARG)
Nuclear receptors [BR:
hsa03310
]
1. Thyroid hormone like
1C. Peroxisome proliferator-activated receptor (PPAR)
5468 (PPARG)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PPARgamma_N
zf-C4
Hormone_recep
Tmemb_55A
Motif
Other DBs
NCBI-GeneID:
5468
NCBI-ProteinID:
NP_056953
OMIM:
601487
HGNC:
9236
Ensembl:
ENSG00000132170
Pharos:
P37231
(Tclin)
UniProt:
P37231
Structure
PDB
LinkDB
All DBs
Position
3:12287368..12434344
Genome browser
AA seq
505 aa
AA seq
DB search
MGETLGDSPIDPESDSFTDTLSANISQEMTMVDTEMPFWPTNFGISSVDLSVMEDHSHSF
DIKPFTTVDFSSISTPHYEDIPFTRTDPVVADYKYDLKLQEYQSAIKVEPASPPYYSEKT
QLYNKPHEEPSNSLMAIECRVCGDKASGFHYGVHACEGCKGFFRRTIRLKLIYDRCDLNC
RIHKKSRNKCQYCRFQKCLAVGMSHNAIRFGRMPQAEKEKLLAEISSDIDQLNPESADLR
ALAKHLYDSYIKSFPLTKAKARAILTGKTTDKSPFVIYDMNSLMMGEDKIKFKHITPLQE
QSKEVAIRIFQGCQFRSVEAVQEITEYAKSIPGFVNLDLNDQVTLLKYGVHEIIYTMLAS
LMNKDGVLISEGQGFMTREFLKSLRKPFGDFMEPKFEFAVKFNALELDDSDLAIFIAVII
LSGDRPGLLNVKPIEDIQDNLLQALELQLKLNHPESSQLFAKLLQKMTDLRQIVTEHVQL
LQVIKKTETDMSLHPLLQEIYKDLY
NT seq
1518 nt
NT seq
+upstream
nt +downstream
nt
atgggtgaaactctgggagattctcctattgacccagaaagcgattccttcactgataca
ctgtctgcaaacatatcacaagaaatgaccatggttgacacagagatgccattctggccc
accaactttgggatcagctccgtggatctctccgtaatggaagaccactcccactccttt
gatatcaagcccttcactactgttgacttctccagcatttctactccacattacgaagac
attccattcacaagaacagatccagtggttgcagattacaagtatgacctgaaacttcaa
gagtaccaaagtgcaatcaaagtggagcctgcatctccaccttattattctgagaagact
cagctctacaataagcctcatgaagagccttccaactccctcatggcaattgaatgtcgt
gtctgtggagataaagcttctggatttcactatggagttcatgcttgtgaaggatgcaag
ggtttcttccggagaacaatcagattgaagcttatctatgacagatgtgatcttaactgt
cggatccacaaaaaaagtagaaataaatgtcagtactgtcggtttcagaaatgccttgca
gtggggatgtctcataatgccatcaggtttgggcggatgccacaggccgagaaggagaag
ctgttggcggagatctccagtgatatcgaccagctgaatccagagtccgctgacctccgg
gccctggcaaaacatttgtatgactcatacataaagtccttcccgctgaccaaagcaaag
gcgagggcgatcttgacaggaaagacaacagacaaatcaccattcgttatctatgacatg
aattccttaatgatgggagaagataaaatcaagttcaaacacatcacccccctgcaggag
cagagcaaagaggtggccatccgcatctttcagggctgccagtttcgctccgtggaggct
gtgcaggagatcacagagtatgccaaaagcattcctggttttgtaaatcttgacttgaac
gaccaagtaactctcctcaaatatggagtccacgagatcatttacacaatgctggcctcc
ttgatgaataaagatggggttctcatatccgagggccaaggcttcatgacaagggagttt
ctaaagagcctgcgaaagccttttggtgactttatggagcccaagtttgagtttgctgtg
aagttcaatgcactggaattagatgacagcgacttggcaatatttattgctgtcattatt
ctcagtggagaccgcccaggtttgctgaatgtgaagcccattgaagacattcaagacaac
ctgctacaagccctggagctccagctgaagctgaaccaccctgagtcctcacagctgttt
gccaagctgctccagaaaatgacagacctcagacagattgtcacggaacacgtgcagcta
ctgcaggtgatcaagaagacggagacagacatgagtcttcacccgctcctgcaggagatc
tacaaggacttgtactag
Homo sapiens (human): 7849
Help
Entry
7849 CDS
T01001
Symbol
PAX8, PAX-8
Name
(RefSeq) paired box 8
KO
K09293
paired box protein 8
Organism
hsa
Homo sapiens (human)
Pathway
hsa04918
Thyroid hormone synthesis
hsa05200
Pathways in cancer
hsa05202
Transcriptional misregulation in cancer
hsa05216
Thyroid cancer
Network
nt06240
Transcription
nt06274
Thyroid cancer
nt06322
TRH-TSH-TH signaling
Element
N00126
PAX8-PPARG fusion to PPARG-mediated transcription
N00782
TSH-TG signaling pathway
Disease
H00032
Thyroid cancer
H00250
Congenital nongoitrous hypothyroidism (CHNG)
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04918 Thyroid hormone synthesis
7849 (PAX8)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
7849 (PAX8)
05202 Transcriptional misregulation in cancer
7849 (PAX8)
09162 Cancer: specific types
05216 Thyroid cancer
7849 (PAX8)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
7849 (PAX8)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Helix-turn-helix
Homeo domain Paired-related
7849 (PAX8)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
PAX
Pax2_C
HTH_23
HTH_32
HTH_38
HTH_Tnp_IS1
HTH_28
Motif
Other DBs
NCBI-GeneID:
7849
NCBI-ProteinID:
NP_003457
OMIM:
167415
HGNC:
8622
Ensembl:
ENSG00000125618
Pharos:
Q06710
(Tbio)
UniProt:
Q06710
R9W7C9
Structure
PDB
LinkDB
All DBs
Position
2:complement(113215997..113278921)
Genome browser
AA seq
450 aa
AA seq
DB search
MPHNSIRSGHGGLNQLGGAFVNGRPLPEVVRQRIVDLAHQGVRPCDISRQLRVSHGCVSK
ILGRYYETGSIRPGVIGGSKPKVATPKVVEKIGDYKRQNPTMFAWEIRDRLLAEGVCDND
TVPSVSSINRIIRTKVQQPFNLPMDSCVATKSLSPGHTLIPSSAVTPPESPQSDSLGSTY
SINGLLGIAQPGSDKRKMDDSDQDSCRLSIDSQSSSSGPRKHLRTDAFSQHHLEPLECPF
ERQHYPEAYASPSHTKGEQGLYPLPLLNSTLDDGKATLTPSNTPLGRNLSTHQTYPVVAD
PHSPFAIKQETPEVSSSSSTPSSLSSSAFLDLQQVGSGVPPFNAFPHAASVYGQFTGQAL
LSGREMVGPTLPGYPPHIPTSGQGSYASSAIAGMVAGSEYSGNAYGHTPYSSYSEAWRFP
NSSLLSSPYYYSSTSRPSAPPTTATAFDHL
NT seq
1353 nt
NT seq
+upstream
nt +downstream
nt
atgcctcacaactccatcagatctggccatggagggctgaaccagctgggaggggccttt
gtgaatggcagacctctgccggaagtggtccgccagcgcatcgtagacctggcccaccag
ggtgtaaggccctgcgacatctctcgccagctccgcgtcagccatggctgcgtcagcaag
atccttggcaggtactacgagactggcagcatccggcctggagtgatagggggctccaag
cccaaggtggccacccccaaggtggtggagaagattggggactacaaacgccagaaccct
accatgtttgcctgggagatccgagaccggctcctggctgagggcgtctgtgacaatgac
actgtgcccagtgtcagctccattaatagaatcatccggaccaaagtgcagcaaccattc
aacctccctatggacagctgcgtggccaccaagtccctgagtcccggacacacgctgatc
cccagctcagctgtaactcccccggagtcaccccagtcggattccctgggctccacctac
tccatcaatgggctcctgggcatcgctcagcctggcagcgacaagaggaaaatggatgac
agtgatcaggatagctgccgactaagcattgactcacagagcagcagcagcggaccccga
aagcaccttcgcacggatgccttcagccagcaccacctcgagccgctcgagtgcccattt
gagcggcagcactacccagaggcctatgcctcccccagccacaccaaaggcgagcagggc
ctctacccgctgcccttgctcaacagcaccctggacgacgggaaggccaccctgacccct
tccaacacgccactggggcgcaacctctcgactcaccagacctaccccgtggtggcagat
cctcactcacccttcgccataaagcaggaaacccccgaggtgtccagttctagctccacc
ccttcctctttatctagctccgcctttttggatctgcagcaagtcggctccggggtcccg
cccttcaatgcctttccccatgctgcctccgtgtacgggcagttcacgggccaggccctc
ctctcagggcgagagatggtggggcccacgctgcccggatacccaccccacatccccacc
agcggacagggcagctatgcctcctctgccatcgcaggcatggtggcaggaagtgaatac
tctggcaatgcctatggccacaccccctactcctcctacagcgaggcctggcgcttcccc
aactccagcttgctgagttccccatattattacagttccacatcaaggccgagtgcaccg
cccaccactgccacggcctttgaccatctgtag
DBGET
integrated database retrieval system