Ornithorhynchus anatinus (platypus): 100092826
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Entry
100092826 CDS
T01045
Symbol
RARA
Name
(RefSeq) retinoic acid receptor alpha isoform X1
KO
K08527
retinoic acid receptor alpha
Organism
oaa
Ornithorhynchus anatinus (platypus)
Pathway
oaa04659
Th17 cell differentiation
oaa04915
Estrogen signaling pathway
oaa05200
Pathways in cancer
oaa05202
Transcriptional misregulation in cancer
oaa05221
Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:
oaa00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
100092826 (RARA)
09152 Endocrine system
04915 Estrogen signaling pathway
100092826 (RARA)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
100092826 (RARA)
05202 Transcriptional misregulation in cancer
100092826 (RARA)
09162 Cancer: specific types
05221 Acute myeloid leukemia
100092826 (RARA)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
oaa03000
]
100092826 (RARA)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
oaa03310
]
100092826 (RARA)
Transcription factors [BR:
oaa03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
100092826 (RARA)
Nuclear receptors [BR:
oaa03310
]
1. Thyroid hormone like
1B. Retinoic acid receptor (RAR)
100092826 (RARA)
BRITE hierarchy
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Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
100092826
NCBI-ProteinID:
XP_028931396
Ensembl:
ENSOANG00000041579
LinkDB
All DBs
Position
11:13697540..13736079
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AA seq
457 aa
AA seq
DB search
MYESVDVGGLGPGPGPSPSPFLMVDFYNQSRSCLLPEKALPGPGPFATPLRTQLWTNSGH
SIETQSTSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKN
MVYTCHRDKGCVINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEPSKAECSESCS
LTPEVEELIGKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDVDLWDKFSELSTKCIIKT
VEFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHN
AGFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDKVDKLQEPLLEAL
KVYVRKRRPNRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGAMPPLIQEMLENSEG
LDTLGGGGGGPGGGPGGSCSPSPSPSSNSSSPATHSP
NT seq
1374 nt
NT seq
+upstream
nt +downstream
nt
atgtacgagagtgtggacgtggggggcctgggccccggccccggccccagccccagccct
ttcctcatggtggatttttacaaccagagccggtcctgcctcctgccggagaaggctctg
cccggccccggccctttcgccaccccgctccggacccagctgtggactaactccggccac
tccatcgagacccagagcacgagttctgaagaaatcgtgcccagccccccttcgccgccg
cccctcccccgcatctacaagccatgcttcgtgtgtcaggacaagtcctcgggctaccac
tacggcgtcagcgcctgcgaaggttgcaaggggttcttccgccgcagcatccagaagaac
atggtgtacacctgccaccgggacaaaggctgcgtcatcaacaaggtgacccggaaccgc
tgccagtactgccgtctgcagaagtgcttcgaagttggcatgtccaaggagtccgtgcgg
aacgaccggaacaagaagaagaaggaaccgtccaaggccgagtgctcggagagctgcagc
ctgacgcccgaggtggaggagctgatcggcaaagtgcgcaaggctcaccaggagaccttc
cctgccctctgccaactgggcaaatacactacgaacaacagctcggagcagcgggtgtcc
ctggacgtggacctgtgggacaagttcagtgaactctccaccaagtgcatcatcaagacg
gtggagttcgccaagcagctgcctggcttcaccacgctcaccatcgccgaccagatcacc
ttgctcaaggccgcctgcctggacatcctgatcctgcgtatctgcacgcggtacacgcca
gagcaggacaccatgaccttctcggacgggctgacgctgaaccggacacagatgcataac
gccggcttcggccccctgaccgacctcgtcttcgccttcgccaaccagctgctgcccctg
gagatggacgacgcggagaccgggctcctcagtgccatctgcctcatctgcggagaccgg
caggacctggagcagccggacaaggtggacaagctgcaggagccgctgctggaggcgctg
aaggtttacgtccgcaagcggagacccaaccggccgcacatgttccccaagatgctgatg
aagatcacggatctgcgaagcatcagcgctaagggagcggaacgtgtgatcacgctgaag
atggagatccccggggccatgccaccgctcatccaggagatgctggagaactccgagggg
ctggacactctgggcgggggcgggggcgggccggggggcgggccggggggcagctgcagc
cccagcccctcccccagctccaacagcagcagcccggccacccactccccgtga
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