Camelus ferus (Wild Bactrian camel): 102503688
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Entry
102503688 CDS
T02979
Symbol
RARA
Name
(RefSeq) retinoic acid receptor alpha isoform X1
KO
K08527
retinoic acid receptor alpha
Organism
cfr
Camelus ferus (Wild Bactrian camel)
Pathway
cfr04659
Th17 cell differentiation
cfr04915
Estrogen signaling pathway
cfr05200
Pathways in cancer
cfr05202
Transcriptional misregulation in cancer
cfr05221
Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:
cfr00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
102503688 (RARA)
09152 Endocrine system
04915 Estrogen signaling pathway
102503688 (RARA)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
102503688 (RARA)
05202 Transcriptional misregulation in cancer
102503688 (RARA)
09162 Cancer: specific types
05221 Acute myeloid leukemia
102503688 (RARA)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
cfr03000
]
102503688 (RARA)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
cfr03310
]
102503688 (RARA)
Transcription factors [BR:
cfr03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
102503688 (RARA)
Nuclear receptors [BR:
cfr03310
]
1. Thyroid hormone like
1B. Retinoic acid receptor (RAR)
102503688 (RARA)
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Ortholog
Paralog
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
102503688
NCBI-ProteinID:
XP_032313869
UniProt:
A0A8B8RA36
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Position
16:49027868..49061924
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AA seq
507 aa
AA seq
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MYESVEVGGLTPTPNPFLVVDFYNQNRACLLPEKGLPAPGPYSTPLRTPLWNGSNHCRWG
PGQGDGTDGGAGGFFDSLILPVWLGSPSFPETASLPWSLNPDSSAIETQSSSSEEIVPSP
PSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNMVYTCHRDKNCIINKV
TRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEAPKPECSESYTLTPEVGELIEKVRKAH
QETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTVEFAKQLPGFTTLTIA
DQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNAGFGPLTDLVFAFANQ
LLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALKVYVRKRRPSRPHMFP
KMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGLDTLSGQAGGGGRDGG
GLAPPPGSCSPSLSPSSNRSSPATHSP
NT seq
1524 nt
NT seq
+upstream
nt +downstream
nt
atgtacgagagtgtggaagtgggggggctcacccccacccccaatcccttcctggtggtg
gatttttataaccagaaccgggcctgtttgctcccggagaaggggctccctgcccccggc
ccctactccaccccactccggactccgctttggaatggctcaaaccactgtaggtggggt
cctgggcaaggagacgggactgatgggggtgctggaggcttctttgacagcctcattctc
ccagtctggctgggaagtcccagctttcctgagactgcgtccctgccctggagtttgaat
cctgacagcagtgccattgagacccagagcagcagttccgaagagatagtgcccagccct
ccctcaccaccaccccttccccgcatctacaagccttgctttgtctgtcaagacaaatcc
tcaggctaccactatggggtcagcgcctgtgagggctgcaagggcttcttccgccgcagc
atccagaagaacatggtgtacacgtgtcaccgggacaagaactgcatcatcaacaaggtg
acccggaaccgctgccagtactgccggctgcagaaatgcttcgaagtgggcatgtccaag
gagtccgtgaggaacgaccggaacaagaagaagaaggaggcacccaagcccgagtgctcc
gagagctacacgctgacgccggaggtgggcgagctcatcgagaaggtgcgcaaagcgcac
caggagaccttccccgccctctgccagctgggcaagtacactacgaacaacagctcagaa
cagcgtgtctctctggacatcgacctctgggacaagttcagtgaactctccaccaagtgc
atcattaagactgtggagttcgccaagcagctgcccggcttcaccaccctcaccatcgct
gaccagatcactctcctcaaggctgcctgcctggacatcctgatcctgcggatctgcacg
cggtacacgcccgagcaggacacgatgaccttctctgacgggctcaccctgaaccggacc
cagatgcacaacgccggcttcggccctctcacagacctggtctttgccttcgccaaccag
ctgctgcccctggagatggatgacgctgagactgggctgctcagcgccatctgcctcatc
tgtggagaccggcaggacctggagcagccagacagagtggacatgctgcaggagccgctg
cttgaggcactgaaggtctatgtgcggaaacggaggcccagccgcccacacatgttcccc
aagatgctaatgaagatcacagacctgcggagcatcagtgctaagggggctgagcgggtg
atcacgctgaaaatggagatcccgggctccatgccacctctcatccaggaaatgctggag
aactcagagggcctggacactctgagcggacaagcggggggtggggggcgggatgggggc
ggcctggctcccccacctggcagctgcagccccagcctcagccccagctccaacagaagc
agcccggccacccactccccgtga
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