Homo sapiens (human): 4929
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Entry
4929 CDS
T01001
Symbol
NR4A2, HZF-3, NOT, NURR1, RNR1, TINUR
Name
(RefSeq) nuclear receptor subfamily 4 group A member 2
KO
K08558
nuclear receptor subfamily 4 group A member 2
Organism
hsa
Homo sapiens (human)
Pathway
hsa04925
Aldosterone synthesis and secretion
hsa04928
Parathyroid hormone synthesis, secretion and action
Disease
H00057
Parkinson disease
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09150 Organismal Systems
09152 Endocrine system
04928 Parathyroid hormone synthesis, secretion and action
4929 (NR4A2)
04925 Aldosterone synthesis and secretion
4929 (NR4A2)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
hsa03000
]
4929 (NR4A2)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
hsa03310
]
4929 (NR4A2)
Transcription factors [BR:
hsa03000
]
Eukaryotic type
Zinc finger
Cys4 nerve growth factor IB-like
4929 (NR4A2)
Nuclear receptors [BR:
hsa03310
]
4. Nerve growth factor IB like
4A. Nerve growth factor IB like receptor
4929 (NR4A2)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
4929
NCBI-ProteinID:
NP_006177
OMIM:
601828
HGNC:
7981
Ensembl:
ENSG00000153234
Vega:
OTTHUMG00000131950
Pharos:
P43354
(Tchem)
UniProt:
P43354
F1D8N6
Q53EL4
Structure
PDB
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All DBs
Position
2:complement(156324437..156332721)
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AA seq
598 aa
AA seq
DB search
MPCVQAQYGSSPQGASPASQSYSYHSSGEYSSDFLTPEFVKFSMDLTNTEITATTSLPSF
STFMDNYSTGYDVKPPCLYQMPLSGQQSSIKVEDIQMHNYQQHSHLPPQSEEMMPHSGSV
YYKPSSPPTPTTPGFQVQHSPMWDDPGSLHNFHQNYVATTHMIEQRKTPVSRLSLFSFKQ
SPPGTPVSSCQMRFDGPLHVPMNPEPAGSHHVVDGQTFAVPNPIRKPASMGFPGLQIGHA
SQLLDTQVPSPPSRGSPSNEGLCAVCGDNAACQHYGVRTCEGCKGFFKRTVQKNAKYVCL
ANKNCPVDKRRRNRCQYCRFQKCLAVGMVKEVVRTDSLKGRRGRLPSKPKSPQEPSPPSP
PVSLISALVRAHVDSNPAMTSLDYSRFQANPDYQMSGDDTQHIQQFYDLLTGSMEIIRGW
AEKIPGFADLPKADQDLLFESAFLELFVLRLAYRSNPVEGKLIFCNGVVLHRLQCVRGFG
EWIDSIVEFSSNLQNMNIDISAFSCIAALAMVTERHGLKEPKRVEELQNKIVNCLKDHVT
FNNGGLNRPNYLSKLLGKLPELRTLCTQGLQRIFYLKLEDLVPPPAIIDKLFLDTLPF
NT seq
1797 nt
NT seq
+upstream
nt +downstream
nt
atgccttgtgttcaggcgcagtatgggtcctcgcctcaaggagccagccccgcttctcag
agctacagttaccactcttcgggagaatacagctccgatttcttaactccagagtttgtc
aagtttagcatggacctcaccaacactgaaatcactgccaccacttctctccccagcttc
agtacctttatggacaactacagcacaggctacgacgtcaagccaccttgcttgtaccaa
atgcccctgtccggacagcagtcctccattaaggtagaagacattcagatgcacaactac
cagcaacacagccacctgcccccccagtctgaggagatgatgccgcactccgggtcggtt
tactacaagccctcctcgcccccgacgcccaccaccccgggcttccaggtgcagcacagc
cccatgtgggacgacccgggatctctccacaacttccaccagaactacgtggccactacg
cacatgatcgagcagaggaaaacgccagtctcccgcctctccctcttctcctttaagcaa
tcgccccctggcaccccggtgtctagttgccagatgcgcttcgacgggcccctgcacgtc
cccatgaacccggagcccgccggcagccaccacgtggtggacgggcagaccttcgctgtg
cccaaccccattcgcaagcccgcgtccatgggcttcccgggcctgcagatcggccacgcg
tctcagctgctcgacacgcaggtgccctcaccgccgtcgcggggctccccctccaacgag
gggctgtgcgctgtgtgtggggacaacgcggcctgccaacactacggcgtgcgcacctgt
gagggctgcaaaggcttctttaagcgcacagtgcaaaaaaatgcaaaatacgtgtgttta
gcaaataaaaactgcccagtggacaagcgtcgccggaatcgctgtcagtactgccgattt
cagaagtgcctggctgttgggatggtcaaagaagtggttcgcacagacagtttaaaaggc
cggagaggtcgtttgccctcgaaaccgaagagcccacaggagccctctcccccttcgccc
ccggtgagtctgatcagtgccctcgtcagggcccatgtcgactccaacccggctatgacc
agcctggactattccaggttccaggcgaaccctgactatcaaatgagtggagatgacacc
cagcatatccagcaattctatgatctcctgactggctccatggagatcatccggggctgg
gcagagaagatccctggcttcgcagacctgcccaaagccgaccaagacctgctttttgaa
tcagctttcttagaactgtttgtccttcgattagcatacaggtccaacccagtggagggt
aaactcatcttttgcaatggggtggtcttgcacaggttgcaatgcgttcgtggctttggg
gaatggattgattccattgttgaattctcctccaacttgcagaatatgaacatcgacatt
tctgccttctcctgcattgctgccctggctatggtcacagagagacacgggctcaaggaa
cccaagagagtggaagaactgcaaaacaagattgtaaattgtctcaaagaccacgtgact
ttcaacaatggggggttgaaccgccccaattatttgtccaaactgttggggaagctccca
gaacttcgtaccctttgcacacaggggctacagcgcattttctacctgaaattggaagac
ttggtgccaccgccagcaataattgacaaacttttcctggacactttacctttctaa
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