KEGG   Hyaena hyaena (striped hyena): 120229003
Entry
120229003         CDS       T07257                                 
Symbol
RARA
Name
(RefSeq) retinoic acid receptor alpha isoform X1
  KO
K08527  retinoic acid receptor alpha
Organism
hhv  Hyaena hyaena (striped hyena)
Pathway
hhv04659  Th17 cell differentiation
hhv04915  Estrogen signaling pathway
hhv05200  Pathways in cancer
hhv05202  Transcriptional misregulation in cancer
hhv05221  Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:hhv00001]
 09150 Organismal Systems
  09151 Immune system
   04659 Th17 cell differentiation
    120229003 (RARA)
  09152 Endocrine system
   04915 Estrogen signaling pathway
    120229003 (RARA)
 09160 Human Diseases
  09161 Cancer: overview
   05200 Pathways in cancer
    120229003 (RARA)
   05202 Transcriptional misregulation in cancer
    120229003 (RARA)
  09162 Cancer: specific types
   05221 Acute myeloid leukemia
    120229003 (RARA)
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hhv03000]
    120229003 (RARA)
  09183 Protein families: signaling and cellular processes
   03310 Nuclear receptors [BR:hhv03310]
    120229003 (RARA)
Transcription factors [BR:hhv03000]
 Eukaryotic type
  Zinc finger
   Cys4 thyroid hormone receptor-like
    120229003 (RARA)
Nuclear receptors [BR:hhv03310]
 1. Thyroid hormone like
  1B. Retinoic acid receptor (RAR)
   120229003 (RARA)
SSDB
Motif
Pfam: zf-C4 Hormone_recep
Other DBs
NCBI-GeneID: 120229003
NCBI-ProteinID: XP_039083638
LinkDB
Position
Unknown
AA seq 462 aa
MASNSSSCPTPGGGHLNGYPVPPYAFFFPPMLGGLSPPGALTTLQHQLPVSGYSTPSPAT
IETQSSSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
VYTCHRDKNCIINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEAPKPECSESYTL
TPEVGELIEKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTV
EFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALK
VYVRKRRPSRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGL
DTLSGQPGGGGRDGGGLAPAPGSCSPSLSPSSNRSSPAAHSP
NT seq 1389 nt   +upstreamnt  +downstreamnt
atggccagtaacagcagctcctgcccaacacctgggggagggcacctcaatgggtacccg
gtgcccccctacgccttcttcttcccgccaatgctgggtggactttcaccgccaggcgcc
ctgaccactctccagcaccagcttccagtcagcggctatagcacaccatccccagccacc
attgagacccagagcagcagttccgaagagatagtgcccagtcctccctcgccgcccccc
ctaccccgcatctacaagccttgctttgtctgtcaagacaaatcctcaggctaccactat
ggggtcagcgcctgtgagggctgtaagggcttcttccgacgcagcatccagaagaacatg
gtgtacacgtgccaccgggacaagaactgcatcatcaacaaggtgacccggaaccgctgc
cagtactgccggctgcagaagtgctttgaagtgggcatgtccaaggagtctgtgaggaac
gacaggaacaagaagaagaaggaggcacccaagcccgagtgctctgagagctacacgctg
acgcctgaggtgggggagctcatcgagaaggtgcgcaaagcgcaccaggaaaccttccct
gccctctgccagctgggcaaatacactacgaacaacagctcagagcaacgtgtttctctg
gacattgacctctgggacaagttcagtgaactctccaccaagtgcatcattaagactgtg
gagttcgccaagcagctgcccggctttaccaccctcaccattgccgaccagatcaccctc
ctcaaggctgcctgcctggacatcctgatcctgcggatctgcacgcggtacacacccgag
caggacacaatgaccttctcagatggtctgaccctgaaccggacccagatgcacaatgcc
ggcttcggccccctcacggacctggtcttcgccttcgccaaccagctgctgcccctggag
atggatgatgctgagactggtcttctcagtgccatctgtctcatctgtggagaccggcag
gacctggagcagccagacagggtggacatgcttcaggagccgctgctggaggcgctgaag
gtctatgtgcggaaacggaggcccagccgccctcacatgttccccaagatgctgatgaag
atcacggacctgcggagcatcagtgctaagggggctgaacgggtgatcacgctgaagatg
gagatcccgggctccatgccacctctcatccaggaaatgctggagaactccgagggcctg
gacactctgagcggacagccggggggcggggggcgggatgggggcggcctggcccccgcc
cctggcagctgtagccccagcctcagccccagctcaaacagaagcagcccggccgcccac
tccccgtga

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