Nannospalax galili (Upper Galilee mountains blind mole rat): 103731122
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Entry
103731122 CDS
T03372
Symbol
Rara
Name
(RefSeq) retinoic acid receptor alpha
KO
K08527
retinoic acid receptor alpha
Organism
ngi
Nannospalax galili (Upper Galilee mountains blind mole rat)
Pathway
ngi04659
Th17 cell differentiation
ngi04915
Estrogen signaling pathway
ngi05200
Pathways in cancer
ngi05202
Transcriptional misregulation in cancer
ngi05221
Acute myeloid leukemia
Brite
KEGG Orthology (KO) [BR:
ngi00001
]
09150 Organismal Systems
09151 Immune system
04659 Th17 cell differentiation
103731122 (Rara)
09152 Endocrine system
04915 Estrogen signaling pathway
103731122 (Rara)
09160 Human Diseases
09161 Cancer: overview
05200 Pathways in cancer
103731122 (Rara)
05202 Transcriptional misregulation in cancer
103731122 (Rara)
09162 Cancer: specific types
05221 Acute myeloid leukemia
103731122 (Rara)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03000 Transcription factors [BR:
ngi03000
]
103731122 (Rara)
09183 Protein families: signaling and cellular processes
03310 Nuclear receptors [BR:
ngi03310
]
103731122 (Rara)
Transcription factors [BR:
ngi03000
]
Eukaryotic type
Zinc finger
Cys4 thyroid hormone receptor-like
103731122 (Rara)
Nuclear receptors [BR:
ngi03310
]
1. Thyroid hormone like
1B. Retinoic acid receptor (RAR)
103731122 (Rara)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
zf-C4
Hormone_recep
Motif
Other DBs
NCBI-GeneID:
103731122
NCBI-ProteinID:
XP_008827658
UniProt:
A0A8C6QAI7
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All DBs
Position
Un
AA seq
462 aa
AA seq
DB search
MASNSSSCPTPGGGHLNGYPVPPYAFFFPPMLGGLSPPGALTSLQHQLPVSGYSTPSPAT
IETQSSSSEEIVPSPPSPPPLPRIYKPCFVCQDKSSGYHYGVSACEGCKGFFRRSIQKNM
VYTCHRDKNCIINKVTRNRCQYCRLQKCFEVGMSKESVRNDRNKKKKEAPKPECSESYTL
TPEVGELIEKVRKAHQETFPALCQLGKYTTNNSSEQRVSLDIDLWDKFSELSTKCIIKTV
EFAKQLPGFTTLTIADQITLLKAACLDILILRICTRYTPEQDTMTFSDGLTLNRTQMHNA
GFGPLTDLVFAFANQLLPLEMDDAETGLLSAICLICGDRQDLEQPDRVDMLQEPLLEALK
VYVRKRRPSRPHMFPKMLMKITDLRSISAKGAERVITLKMEIPGSMPPLIQEMLENSEGL
DTLSGQPGGGTRDGGGLAPPPGSCSPSLSPSSHRSSPATQSP
NT seq
1389 nt
NT seq
+upstream
nt +downstream
nt
atggccagcaatagcagctcctgcccaacacctgggggcgggcacctcaatgggtacccg
gtgcccccctacgccttcttcttcccccctatgctgggtggactctccccaccaggtgct
ctcacctctctccagcaccagcttccagttagtggatacagcacaccttccccagccacc
atcgagactcagagcagcagttcagaagagatagtgcccagccctccctcgccgccaccc
ctgccccgaatctacaagccctgttttgtctgtcaggacaaatcctcgggctaccactat
ggggtcagtgcctgtgagggctgcaagggcttcttccgccgcagtatccagaagaacatg
gtatacacgtgtcaccgggacaagaactgcattatcaacaaggtgacccggaaccgctgc
cagtactgccggctgcagaaatgtttcgaagtgggcatgtccaaggagtctgtgcgaaat
gaccgaaacaagaagaagaaggaggcacctaagccagagtgctcagagagctacacgcta
acgccggaggtcggggagctcatcgagaaggtgcgaaaagcacaccaggagaccttccct
gccctctgccagctgggcaagtacactacgaacaacagctcagaacaacgtgtctctctg
gacattgacctctgggacaagttcagtgaactttccaccaagtgcatcattaagactgtg
gagttcgccaagcagctgcccggcttcaccaccctcaccattgccgaccagatcaccctc
ctcaaggctgcctgcctggatatcctgatcctgcggatctgcacgcggtacacgcctgag
caagacacaatgaccttctcagatgggctgaccctgaaccggacccagatgcacaatgct
ggctttggccccctcaccgacttggtctttgcctttgccaaccagctgctgcccctagag
atggatgatgctgagactgggttgctcagcgccatctgcctcatctgtggagatcggcag
gacctggagcagccggacagggtggacatgctgcaggagcccctgctcgaggcactcaag
gtctatgtgaggaaacggaggcccagccgcccccatatgttccctaagatgctgatgaag
atcacagaccttcggagtatcagcgccaagggggccgagcgagtgatcacgctgaagatg
gagataccgggctccatgccaccactcatccaggaaatgctggagaactcagagggctta
gacactctgagtggacagccggggggtgggacacgagacgggggaggactggctcccccg
ccaggcagctgtagccccagcctcagccccagctcccacagaagcagcccagccacccag
tctccatga
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