Panthera tigris altaica (Amur tiger): 102958009
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Entry
102958009 CDS
T02988
Symbol
MEN1
Name
(RefSeq) menin 1
KO
K14970
menin
Organism
ptg
Panthera tigris altaica (Amur tiger)
Pathway
ptg04934
Cushing syndrome
ptg05202
Transcriptional misregulation in cancer
Brite
KEGG Orthology (KO) [BR:
ptg00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
102958009 (MEN1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
102958009 (MEN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
ptg03036
]
102958009 (MEN1)
Chromosome and associated proteins [BR:
ptg03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
102958009 (MEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
102958009
NCBI-ProteinID:
XP_007092145
LinkDB
All DBs
Position
Un
AA seq
565 aa
AA seq
DB search
MPRPAAMGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVI
PTNVPELTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSS
RELVKKVSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVH
LALSEDHAWVVFGPNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKM
EVAFMVCAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPG
RPDPLTLYHKGIASAKTYYRDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQDYNYC
REDEEIYKEFFEVANDVIPNLLKEAASLLEAGEERPGEQTQGAQSQSSALQDPECFAHLL
RFYDGICKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVRIVSREAEAAEAEELWGEE
AREGRRRGPRRESKSEQTSFRPSGNLPEVQPPQGTLEEICRGLRARDTVTSELAAVKIVK
VDPGEGLEAGPLRWWEGIAPGGAES
NT seq
1698 nt
NT seq
+upstream
nt +downstream
nt
atgccgaggcccgccgccatggggctgaaggccgcccagaagacgctgttcccgctgcgc
tccatcgacgacgtggtgcgcctgttcgctgccgagctgggccgagaggaaccggacctg
gtgctcctgtccttggtactgggcttcgtggagcatttcctagctgtcaaccgcgtcatc
cccaccaatgtgcccgagctcaccttccagcccagccccgcgcccgaccctcctggcggc
cttacctacttccccgtggccgacctgtccatcatcgccgcgctgtatgcccgcttcacc
gcccagatccgtggcgccgtcgacctgtctctctacccgcgagaggggggtgtctccagc
cgagaactggtgaagaaggtctccgatgtcatctggaacagcctcagccgctcctacttc
aaggatcgggcccacatccagtccctcttcagcttcatcacaggcactaaactggacagt
tctggtgtggcctttgccgtggtgggggcctgccaggctctgggtctccgggatgtccac
ctcgccctgtctgaggaccacgcctgggtagtgtttgggcccaacggagaacagacagct
gaggtcacctggcacggcaagggcaacgaggatcgcaggggccagacggtcaacgcgggt
gtggccgagcggagctggctgtacctgaaaggatcgtacatgcgctgcgaccgcaagatg
gaggtggcatttatggtgtgtgccatcaacccttccattgacctgcacaccgactccctg
gaactgctgcagctgcagcagaagctgctctggctgctctacgacctgggacatctggaa
aggtaccccatggcgctggggaacctggcagatctggaggaactggaacccacccctggc
cgaccagacccactcaccctctaccacaagggcattgcctcggccaagacctactaccgg
gatgagcacatctacccctacatgtacctggctggctaccactgtcgcaaccgcaacgtg
cgcgaagccctgcaggcctgggctgacacggccactgtcatccaggactacaactactgc
cgcgaggacgaggagatctacaaggagttcttcgaagtagctaatgatgtcatccccaac
ctgctgaaggaggcagctagcctgctggaggccggcgaggagcggccgggggagcagacc
cagggtgcccagagccagagttccgccctccaggatccagagtgcttcgcccacctgctg
cgattctatgatggcatctgcaaatgggaagagggcagccccacgcccgtgctgcacgtg
ggctgggccaccttcctcgtgcagtccctaggccgatttgaggggcaggtgcggcagaag
gtgcgcatagtgagccgcgaggccgaggcggccgaggcggaagagctgtggggcgaggaa
gcccgggaaggacggcggcgaggcccgcggcgtgagtccaaatcagagcagacctctttc
cgaccctctgggaacctccccgaggtccagccgcctcaagggactctggaggaaatctgc
aggggtttgcgagcccgagacacggtcacgtccgaactggccgcggtcaagatagtcaag
gtagacccaggtgagggcctggaggcagggcctctgcgctggtgggagggcatagcgcct
ggtggcgctgagagttga
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