Macaca mulatta (rhesus monkey): 106995582
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Entry
106995582 CDS
T01028
Symbol
MEN1
Name
(RefSeq) menin isoform X1
KO
K14970
menin
Organism
mcc
Macaca mulatta (rhesus monkey)
Pathway
mcc04934
Cushing syndrome
mcc05202
Transcriptional misregulation in cancer
Brite
KEGG Orthology (KO) [BR:
mcc00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
106995582 (MEN1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
106995582 (MEN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
mcc03036
]
106995582 (MEN1)
Chromosome and associated proteins [BR:
mcc03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
106995582 (MEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
106995582
NCBI-ProteinID:
XP_028689092
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All DBs
Position
14:9727989..9735457
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AA seq
637 aa
AA seq
DB search
MGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVIPTNVPE
LTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSSRELVKK
VSDVIWNSLSRSYFKDRAHIQSLFSFITGWSPVGTKLDSSGVAFAVVGACQALGLRDVHL
ALSEDHAWVVFGPNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKME
VAFMVCAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPGR
PDPLTLYHKGIASAKTYYRDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQESLGLP
PMARPLQTLQRPHCSHSYNYCREDEEIYKEFFEVANDVIPNLLKEAASLLEAGEERPGEQ
SQGTQSQGSALQDPECFAHLLRFYDGICKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQ
KVRIVSREAEAAEAEEPWGEEAREGRRRGPRRESKPEEPPPPKKPALDKGLGASQGAVSG
PPRKPPGTVPGTARGPEGGSTAQVPAPAASPPPEGPVLTFQSEKMKGMKELLVATKINSS
AIKLQLTAQSQVQMKKQKVSTPSDYTLSFLKRQRKGL
NT seq
1914 nt
NT seq
+upstream
nt +downstream
nt
atggggctgaaggccgcccagaagacgctgttcccgctgcgctccatcgacgacgtggtg
cgcctgtttgctgccgagctgggccgagaggagccggacctggtgctcctttccttggtg
ctgggcttcgtggagcattttctggctgtcaaccgcgtcatccccaccaacgttcccgag
ctcaccttccagcccagccccgcccccgacccgcctggcggcctcacctactttcccgtg
gccgacctgtctatcatcgccgccctctatgcccgcttcaccgcccagatccgaggcgcc
gtcgacctgtccctctatcctcgagaagggggtgtctccagccgtgagctggtgaagaag
gtctccgatgtcatatggaacagcctcagccgctcctacttcaaggatcgagcccacatc
cagtccctcttcagcttcatcacaggttggagcccagtaggcaccaaattggacagctcc
ggtgtggcctttgctgtggttggggcctgccaggccctgggtctccgggatgtccacctc
gccctgtctgaggatcatgcctgggtagtgtttgggcccaatggggagcagacagctgag
gtcacctggcatggcaagggcaacgaggaccgcaggggccagacggtcaacgctggtgtg
gctgagcggagctggctgtacctgaaaggatcatacatgcgctgtgaccgcaagatggag
gtggcattcatggtgtgtgccatcaacccttccattgacctgcacaccgactcgctggag
ctgctgcagctgcagcagaagctgctctggctgctctatgacctgggacatctggaaagg
taccccatggccttagggaacctggcagatctggaggagctggagcccacccctggccgg
ccagatccactcaccctctaccacaagggcattgcctcagccaagacctactatcgggat
gaacacatctacccctacatgtacctggctggctaccactgtcgcaaccgcaacgtgcgc
gaagccctgcaggcctgggcagacacggccactgtcatccaggagtccctggggctaccc
cccatggcgagaccccttcagaccctacagagaccccactgctctcacagctacaactac
tgccgggaagacgaggagatctacaaggagttcttcgaagtagccaatgatgtcatcccc
aacctgctgaaggaggcagccagcttgctggaggcgggcgaggagcggccgggggagcag
agccagggcacccagagccaaggttctgccctccaggaccctgagtgcttcgcccacctg
ctgcgattctacgacggcatctgcaaatgggaggagggcagtcccacacctgtgctgcac
gtgggctgggccacctttcttgtgcagtccctaggccgtttcgagggacaggtgcggcag
aaggtgcgcatagtgagccgagaggccgaggcagctgaggccgaggagccatggggcgag
gaagcccgggaaggccggcggcggggcccacggcgggagtccaagccagaggagcccccg
ccacccaagaagccagcactggacaagggcctgggtgccagccagggtgcagtgtcagga
cccccccggaagccccctgggacggtccctggcacagcccgaggccctgaaggtggcagc
acggctcaggtgccagcgcctgcagcgtcaccaccgccagagggtccagtgctcactttc
cagagtgagaagatgaagggcatgaaggagctgctggtggccaccaagatcaactcgagc
gccatcaagctgcaactcacggcacagtcacaagtgcagatgaagaagcagaaagtgtcc
acccctagtgactacactctgtctttcctcaagcggcagcgcaaaggcctctaa
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