Talpa occidentalis (Iberian mole): 119232992
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Entry
119232992 CDS
T07495
Symbol
RARA
Name
(RefSeq) retinoic acid receptor alpha isoform X1
KO
K08527
retinoic acid receptor alpha
Organism
tod
Talpa occidentalis (Iberian mole)
Pathway
tod04659
Th17 cell differentiation
tod04915
Estrogen signaling pathway
tod05200
Pathways in cancer
tod05202
Transcriptional misregulation in cancer
tod05221
Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:
tod00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
119232992 (RARA)
09152 Endocrine system
04915 Estrogen signaling pathway
119232992 (RARA)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
119232992 (RARA)
05202 Transcriptional misregulation in cancer
119232992 (RARA)
09162 Cancer: specific types
05221 Acute myeloid leukemia
119232992 (RARA)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
tod03000
]
119232992 (RARA)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
tod03310
]
119232992 (RARA)
Transcription factors [BR:
tod03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
119232992 (RARA)
Nuclear receptors [BR:
tod03310
]
1. Thyroid hormone like
1B. Retinoic acid receptor (RAR)
119232992 (RARA)
BRITE hierarchy
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Ortholog
Paralog
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
119232992
NCBI-ProteinID:
XP_037351275
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Position
Unknown
AA seq
525 aa
AA seq
DB search
MASNSSSCPTPGGGHLSGYPVPPYAFFFPPMLGGLSPPGTLTSLQHQLPVSGYSTPSPAT
IETQSSSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
VYTCHRDKNCIINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEAPKPECSESYTL
TPEVGELIEKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTV
EFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALK
VYVRKRRPSRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGL
DTLSGQPGVGGGTGAGWLPRPAAVAPASAPARTEAARPPTLRDHCARGPGPRPTPWLLSA
FIPTMRPLPAPPRTVLPFLGDGREEAATLQTEAAPGWTARSRSPG
NT seq
1578 nt
NT seq
+upstream
nt +downstream
nt
atggccagcaacagcagctcctgcccgacacctgggggagggcacctcagtgggtacccg
gtgcccccctacgccttcttcttcccccctatgctgggtggactgtctccgccgggcacc
ctgacctctctccagcaccagcttccagttagcggctatagtacaccatccccagccacc
atcgagacccagagcagcagttcagaggagatcgtgcccagccccccctcgccgcccccc
ctcccccgaatctacaagccttgctttgtctgtcaggacaaatcctcaggctaccactat
ggggtcagcgcctgtgagggctgcaagggcttcttccgccgcagtatccagaagaacatg
gtgtacacatgtcaccgagacaagaactgtatcatcaacaaggtgacccggaaccgctgc
cagtactgccggctgcagaagtgcttcgaagtgggcatgtccaaggagtctgtgaggaac
gaccggaacaagaagaagaaggaagcccccaagcctgagtgctcagagagctacaccctg
acgccagaggtgggggagctcatcgagaaagtgcgcaaggcgcatcaggagaccttcccc
gccctctgccagctgggcaaatacactacgaacaacagctcagaacaacgtgtctctctg
gacattgacctctgggacaagttcagtgaactctccaccaagtgcatcattaagaccgtg
gagttcgccaagcaactgcccggcttcaccaccctcaccattgccgaccagatcaccctc
ctcaaggctgcctgcctggacatcctgatcctgcggatctgcacgaggtacacacctgag
caggacacgatgaccttctcggatgggttgaccctgaaccggacccagatgcacaacgcc
ggctttggccccctcacggacctggtcttcgccttcgccaaccagctgctgcctctggag
atggatgatgctgagactggcctgctcagtgccatctgcctcatctgtggagaccggcag
gacctggagcagccagacagggtggacatgctgcaggagccgctgctcgaggcactgaag
gtctacgtgcggaaacggaggcccagccgcccccacatgttccccaagatgctgatgaag
atcaccgacttacgaagcatcagcgctaagggggccgagcgggtgatcacgctgaagatg
gagatcccgggctccatgccacctctcatccaggaaatgctggagaactcggagggcctg
gacactctgagcggacagccgggggtggggggcgggacgggggcgggctggctcccccgc
ccggcagctgtagccccagcctcagccccagctcgaacagaagcagcccggccacccact
ctccgtgaccactgcgcccgtggacctggccctcgccccacgccctggcttctctctgcc
tttataccaaccatgcggcccctgccagccccgccccgcactgtcctccctttcctgggg
gacgggagggaggaggcagcgactcttcagacagaggctgcgccaggatggactgcccgc
tcccgaagcccgggctga
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