Rhinopithecus bieti (black snub-nosed monkey): 108534716
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Entry
108534716 CDS
T04641
Symbol
RARA
Name
(RefSeq) retinoic acid receptor alpha isoform X1
KO
K08527
retinoic acid receptor alpha
Organism
rbb
Rhinopithecus bieti (black snub-nosed monkey)
Pathway
rbb04659
Th17 cell differentiation
rbb04915
Estrogen signaling pathway
rbb05200
Pathways in cancer
rbb05202
Transcriptional misregulation in cancer
rbb05221
Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:
rbb00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
108534716 (RARA)
09152 Endocrine system
04915 Estrogen signaling pathway
108534716 (RARA)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
108534716 (RARA)
05202 Transcriptional misregulation in cancer
108534716 (RARA)
09162 Cancer: specific types
05221 Acute myeloid leukemia
108534716 (RARA)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
rbb03000
]
108534716 (RARA)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
rbb03310
]
108534716 (RARA)
Transcription factors [BR:
rbb03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
108534716 (RARA)
Nuclear receptors [BR:
rbb03310
]
1. Thyroid hormone like
1B. Retinoic acid receptor (RAR)
108534716 (RARA)
BRITE hierarchy
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Ortholog
Paralog
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
108534716
NCBI-ProteinID:
XP_017735690
UniProt:
A0A2K6KLM4
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All DBs
Position
Unknown
AA seq
462 aa
AA seq
DB search
MASNSSSCPTPGGGHLNGYPVPPYAFFFPPMLGGLSPPGALTTLQHQLPVSGYSTPSPAT
IETQSSSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
VYTCHRDKNCIINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEVPKPECSESYTL
TPEVGELIEKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTV
EFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALK
VYVRKRRPSRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGL
DTLSGQPGGGGRDGGGLAPPPGSCSPSLSPSSNRSSPATHSP
NT seq
1389 nt
NT seq
+upstream
nt +downstream
nt
atggccagcaacagcagctcctgcccgacacctgggggcgggcacctcaatgggtacccg
gtgcctccctacgccttcttcttcccccctatgctgggtggactctctccgccaggcgct
ctgaccactctccagcaccagcttccagttagtggatatagcacaccatccccagccacc
attgagacccagagcagcagttctgaagagatagtgcccagccctccctcgccgccccct
ctaccccgcatctacaagccttgctttgtctgtcaggacaagtcctcaggctaccactat
ggggtcagcgcctgtgagggctgcaagggcttcttccgccgcagcatccagaagaacatg
gtgtacacgtgtcaccgggacaagaactgcatcatcaacaaggtgacccggaaccgctgc
cagtactgccgactgcagaagtgcttcgaagtgggcatgtccaaggagtctgtgagaaat
gaccgaaacaagaagaagaaggaggtgcccaagcccgagtgctccgagagctacacgctg
acgccggaggtgggggagctcattgagaaggtgcgcaaagcgcaccaggaaaccttccct
gccctctgccagctgggcaaatacactacgaacaacagctcagaacaacgtgtctctctg
gacattgacctctgggacaagttcagtgaactctccaccaagtgcatcattaagactgtg
gagttcgccaagcagctgcccggcttcaccaccctcaccatcgccgaccagatcaccctc
ctcaaggctgcctgcctggacatcctgatcctgcggatctgcacgcggtacacacccgag
caggacaccatgaccttctccgacgggctgaccctgaaccggacccagatgcacaacgct
ggcttcggccccctcaccgacctggtctttgccttcgccaaccagctgctgcccctggag
atggatgatgcggagacggggctgctcagcgccatctgcctcatctgcggagaccgccag
gacctggagcagcctgaccgcgtggacatgctgcaggagccgctgctggaggcgctaaag
gtctacgtgcgaaagcggaggcccagccgcccccacatgttccccaagatgctgatgaag
atcactgacctgcgaagcatcagcgccaagggggctgagcgggtgatcacgctgaagatg
gagatcccgggctccatgccgcctctcatccaggaaatgctggagaactcagagggcctg
gacactctgagcggacaaccggggggtggggggcgggacgggggtggcctggccccccct
ccaggcagctgtagccccagcctcagccccagctccaacagaagcagcccggccacccac
tccccgtga
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