Rattus norvegicus (rat): 29417
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Entry
29417 CDS
T01003
Symbol
Men1
Name
(RefSeq) menin
KO
K14970
menin
Organism
rno
Rattus norvegicus (rat)
Pathway
rno04934
Cushing syndrome
rno05202
Transcriptional misregulation in cancer
Brite
KEGG Orthology (KO) [BR:
rno00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
29417 (Men1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
29417 (Men1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
rno03036
]
29417 (Men1)
Chromosome and associated proteins [BR:
rno03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
29417 (Men1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
29417
NCBI-ProteinID:
NP_062081
RGD:
3078
Ensembl:
ENSRNOG00000021054
UniProt:
Q9WVR8
LinkDB
All DBs
Position
1:213068166..213074132
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AA seq
610 aa
AA seq
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MGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVIPTNVPE
LTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSSRELVKK
VSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED
HAWVVFGSNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKMEVAFMV
CAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPGRPDPLT
LYHKGIASAKTYYQDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQDYNYCREDEEI
YKEFFEVANDVIPNLLKEAASLLEAGEERPGEQAQGTQGQGSALQDPECFAHLLRFYDGI
CKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVHIVSREAEAAEAEEPWGDEAREGRR
RGPRRESKPEEPPPPKKPALDKGPGSGQSAGSGPPRKTSGTVSGTARGTEVSSAAQAPAP
AASPPPEGPVLTFQSEKMKGMKELLVATKINSSAIKLQLTAQSQVQMKKQKVSTPSDYTL
SFLKRQRKGL
NT seq
1833 nt
NT seq
+upstream
nt +downstream
nt
atggggctgaaggccgcccagaagacgctgttccctctgcgctctatcgacgacgtggtg
cgcctgttcgctgcggagctgggccgagaggagcctgacctggtgctcctctccttggtt
ctgggcttcgtagagcatttcctggctgtcaaccgtgtcatccccaccaacgtgccggag
ctcaccttccagcccagcccggcacccgaccctcctggtggcctcacctacttcccagtg
gccgacctatccatcattgctgccctctatgcccgattcaccgctcagatccgcggtgct
gtggacctctccctctatcctcgagaggggggcgtttccagtcgcgaactggtaaaaaag
gtctcggatgtcatatggaacagcctcagccgctcctacttcaaggaccgggcccacatc
cagtctctcttcagcttcatcacaggcactaaactggacagttcgggcgtggcctttgca
gtggtaggggcctgccaggctctaggtctcagagatgtccatctggccctgtccgaggat
catgcctgggtggtgttcgggtccaatggggaacagacggctgaggtgacctggcatggc
aaaggcaacgaggaccgcagaggccagacagtcaacgctggtgtggctgagcggagctgg
ctgtacctgaaaggatcgtacatgcgctgtgaccgcaagatggaggtggcgttcatggtg
tgtgccatcaacccttccattgatcttcacactgactctttggaactgttgcaactacag
cagaagctgctctggctgctgtatgacctaggacatctggaaaggtaccccatggcgcta
gggaacttggcagacctggaggagctggaacccacccctggtcggccagacccgctcacc
ctctatcacaaggggattgcctcagctaagacctactaccaggatgaacacatctacccc
tacatgtacctggctggataccattgtcgcaaccgcaatgtgcgtgaagccctgcaggcc
tgggccgacactgccactgttatccaagactacaactactgtcgggaggatgaagagatc
tacaaggaattctttgaagtggccaatgacgtcatccccaacctgctgaaggaggcagcc
agcctgctagaagcaggcgaggagcggccaggagagcaagcccagggcacccaaggccaa
ggttctgccctccaggacccagagtgctttgcccacctgctgcgattctatgatggcatc
tgcaaatgggaggagggtagccccacaccagtactgcacgtgggctgggcaactttcctt
gtgcagtccctaggacgctttgagggacaggtgcggcagaaggtgcacatagttagccgg
gaagccgaggcagcagaggcggaagaaccatggggggacgaagcccgagaaggtcgtcgg
cgcggtccccgccgagagtccaagcctgaggagccaccaccacccaagaagcctgcgttg
gacaagggcccaggctcagggcaaagtgcagggtcgggacctcctaggaaaacgtcaggg
actgtctcaggtactgcccgtggcacagaagtcagcagtgctgctcaggctccagcacct
gcagcatcgccacccccagagggcccagtgctcactttccagagtgagaagatgaaagga
atgaaggagctactggtggccaccaagatcaactctagtgccatcaagctgcaactcacg
gcacagtcccaagtgcagatgaagaaacagaaggtgtccacacccagcgactacacactc
tctttcctaaagcggcagcgcaagggcctctga
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