Puma yagouaroundi (jaguarundi): 121023668
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Entry
121023668 CDS
T07555
Symbol
MEN1
Name
(RefSeq) menin isoform X1
KO
K14970
menin
Organism
pyu
Puma yagouaroundi (jaguarundi)
Pathway
pyu04934
Cushing syndrome
pyu05202
Transcriptional misregulation in cancer
Brite
KEGG Orthology (KO) [BR:
pyu00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
121023668 (MEN1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
121023668 (MEN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
pyu03036
]
121023668 (MEN1)
Chromosome and associated proteins [BR:
pyu03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
121023668 (MEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
121023668
NCBI-ProteinID:
XP_040321575
LinkDB
All DBs
Position
Unknown
AA seq
616 aa
AA seq
DB search
MPRPAAMGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVI
PTNVPELTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSS
RELVKKVSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVH
LALSEDHAWVVFGPNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKM
EVAFMVCAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPG
RPDPLTLYHKGIASAKTYYRDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQDYNYC
REDEEIYKEFFEVANDVIPNLLKEAASLLEAGEERPGEQTQGAQSQSSALQDPECFAHLL
RFYDGICKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVRIVSREAEAAEAEELWGEE
AREGRRRGPRRESKPEEPPPPKKPALDKGPGSGQGATSGPPRKPPGTVPGTARGPEGGGA
APAPAPAASPPPEGPVLTFQSEKMKGMKELLVATKINSSAIKLQLTAQSQVQMKKQKVST
PSDYTLSFLKRQRKGL
NT seq
1851 nt
NT seq
+upstream
nt +downstream
nt
atgccgaggcccgccgccatggggctgaaggccgcccagaagacgctgttcccgctgcgc
tccatcgacgacgtggtgcgcctgttcgctgccgagctgggccgggaggaaccggacctg
gtgctcctatccttggtactgggcttcgtggagcatttcctagctgtcaaccgcgtcatc
cccaccaatgtgcccgagctcaccttccagcccagccccgcgcccgaccctcctggcggc
cttacctacttccccgtggccgacctgtccatcatcgccgcgctgtatgcccgcttcacc
gcccagatccgtggcgccgtcgacctgtctctctacccgcgagaggggggtgtctccagc
cgagaactggtgaagaaggtctccgatgtcatctggaacagcctcagccgctcctacttc
aaggatcgggcccacatccagtccctcttcagcttcatcacaggcactaaactggacagt
tctggtgtggcctttgccgtggtgggggcctgccaggctctgggtctccgggatgtccac
ctcgccctgtctgaggaccacgcctgggtagtgtttgggcccaacggagaacagacagct
gaggtcacttggcacggcaagggcaacgaggatcgcaggggccagacggtgaacgcgggt
gtggccgagcggagctggctgtacctgaaaggatcgtacatgcgctgtgaccgcaagatg
gaggtggcgtttatggtgtgtgccatcaacccttccattgacctgcacaccgactccctg
gagctgctgcagctgcagcagaagctgctctggctgctctatgacctgggacatctggaa
aggtaccccatggcactggggaacctggcagatctggaggaactggaacccacccctggc
cgaccagacccactcaccctctaccacaagggcattgcctcggccaagacctactaccgg
gatgagcacatctacccctacatgtacctggccggctaccactgtcgcaaccgcaatgtg
cgcgaagccctgcaggcctgggctgacacggccactgtcatccaggactacaactactgc
cgcgaggacgaggagatctacaaggagttctttgaagtagctaatgatgtcatccccaac
ctgctgaaggaggcagctagcctgctggaggccggcgaggagcggccaggggagcagaca
cagggtgcccagagccagagttccgccctccaggatccagagtgcttcgcccatctgctg
cgattctatgatggcatctgcaaatgggaagagggcagccccacgcccgtgctgcacgtg
ggctgggccaccttcctcgtgcagtccctaggccgatttgaggggcaggtgcggcagaag
gtgcgcatagtgagccgcgaggccgaggcggccgaggcggaggagctgtggggcgaggaa
gcccgggaaggacggcggcgaggcccacggcgtgagtccaagccagaggagccgccgccg
cctaagaaaccggcgctggacaagggcccgggctccggccagggtgccacgtcaggaccc
ccgcggaaacccccagggacagtcccgggcactgcccgcggcccagaaggaggcggcgcg
gctccagcccctgcgcccgcagcgtcgccaccaccggaggggccggtgctcactttccag
agcgagaagatgaagggcatgaaggagctgctggtggccaccaagatcaactcgagcgcc
atcaagctgcagctcacggcgcagtcgcaagtgcagatgaagaagcagaaggtgtctaca
cctagcgactacactctttccttcctcaagcgccagcgcaaaggcctctga
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