Rousettus aegyptiacus (Egyptian rousette): 107517161
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Entry
107517161 CDS
T06036
Symbol
MEN1
Name
(RefSeq) menin isoform X1
KO
K14970
menin
Organism
ray
Rousettus aegyptiacus (Egyptian rousette)
Pathway
ray04934
Cushing syndrome
ray05202
Transcriptional misregulation in cancer
Brite
KEGG Orthology (KO) [BR:
ray00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
107517161 (MEN1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
107517161 (MEN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
ray03036
]
107517161 (MEN1)
Chromosome and associated proteins [BR:
ray03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
107517161 (MEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
107517161
NCBI-ProteinID:
XP_016013073
LinkDB
All DBs
Position
Unknown
AA seq
630 aa
AA seq
DB search
MPTRPSFPRLACRPRPAAMGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLG
FVEHFLAVNRVIPTNVPELTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVD
LSLYPREGGVSSRELVKKVSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVV
GACQALGLRDVHLALSEDHAWVVFGPNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLY
LKGSYMRCDRKMEVAFMVCAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGN
LADLEELEPTPGRPDPLTLYHKGIASAKTYYRDEHIYPYMYLAGYHCRNRNVREALQAWA
DTATVIQDYNYCREDEEIYKEFFEVANDVIPNLLKEAASLLEAGEERPGEQTQGSQSQGS
ALQDPECFAHLLRFYDGICKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVRIVSRES
EAAEAEEPWGEEAREGRRRGPRRESKPEEPPPPKKPALDKGPGAGQSAVPAPPRKSPGTV
PSTARGSEGGGVAPAPAPAPTASPPPEGPVLTFQSEKMKGMKELLVATKINSSAIKLQLT
AQSQVQMKKQKVSTPSDYTLSFLKRQRKSL
NT seq
1893 nt
NT seq
+upstream
nt +downstream
nt
atgcccacccgaccctccttcccccggctcgcctgcaggccgaggcccgccgccatgggg
ctgaaggccgcccagaagacactattcccgctgcgctccatcgacgacgtggtgcgcctg
tttgcagccgagctgggccgagaagagccggacctggtgctcctatccttggtactaggc
tttgtggagcatttcctagctgtcaaccgcgtcatccccaccaatgtgccagagctcacc
ttccagcccagccctgcgcccgaccctcctggcggcctcacctacttcccagttgccgac
ctatccatcatcgctgcgctctatgcccgcttcaccgcccagatccgaggtgccgtcgac
ctgtctctgtacccccgagaagggggcgtctccagccgggagctggtgaagaaagtctcc
gatgtcatctggaacagcctcagccgctcctacttcaaggatcgggcccacatccaatct
ctcttcagcttcatcacaggcaccaaactggacagctctggtgtggcctttgctgtggtg
ggggcctgccaggctctgggtctccgggatgtccacctggccctgtctgaggatcatgcg
tgggtagtgtttgggcccaatggagaacagacagctgaggtcacctggcacggcaagggc
aatgaggaccgcaggggccagacagtcaacgcgggcgtggccgaacggagctggctgtac
ttgaaaggatcatacatgcgctgtgaccgaaagatggaagtggcattcatggtgtgtgcc
atcaacccttccattgacctgcacaccgactcgctggaactactgcagctgcagcagaag
ctgctctggctgctctatgacctgggacatctggaaaggtaccccatggcactggggaac
ctagcagacctggaggagctggagcccacccccggccggccagacccactcaccctctac
cacaagggcattgcttcagccaagacctactaccgggatgagcacatctacccctacatg
tatctggccggctaccattgtcgcaaccgcaatgtgcgcgaagccctacaggcctgggcc
gacactgccactgtcatccaggactacaactactgccgggaggatgaggagatctacaag
gaattctttgaagtagccaatgatgtcatccccaacctgctgaaggaggcagccagcctg
ctggaggccggagaggagcggcccggggagcagacccagggctcccagagccaggggtct
gccctccaggacccagagtgctttgctcatctgctgcggttctacgatggcatctgcaaa
tgggaagagggcagccccacgccggtgctgcacgtgggctgggccaccttccttgtgcag
tccctagggcgtttcgaaggacaggtgcggcaaaaggtgcgcatagtgagccgtgagtcg
gaggccgcggaggcagaggagccgtggggcgaggaagcccgggagggccggcgacggggc
cctcggcgggagtccaagcccgaagagccaccgccacccaagaagccggcgctggacaag
ggtccaggtgcgggtcagagtgcggtgccagcaccccctcggaagtctccagggactgtc
ccgagcactgctcgtggatctgaaggtggcggtgtggctccagcaccagcaccggcgccc
accgcgtcgccgccaccagagggtccggttctcactttccagagtgagaaaatgaagggc
atgaaggagctgctggtagccaccaagatcaactcgagcgccatcaagctgcagctcacc
gcccaatcacaagtgcagatgaaaaagcagaaggtgtctacacccagcgactacactctt
tctttcctcaagaggcagcgcaagagcctctga
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