KEGG   Rattus norvegicus (rat): 29417
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)
SSDB
Motif
Pfam: Menin
Other DBs
NCBI-GeneID: 29417
NCBI-ProteinID: NP_062081
RGD: 3078
Ensembl: ENSRNOG00000021054
UniProt: Q9WVR8
Position
1:213068166..213074132
AA seq 610 aa
MGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVIPTNVPE
LTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSSRELVKK
VSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED
HAWVVFGSNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKMEVAFMV
CAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPGRPDPLT
LYHKGIASAKTYYQDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQDYNYCREDEEI
YKEFFEVANDVIPNLLKEAASLLEAGEERPGEQAQGTQGQGSALQDPECFAHLLRFYDGI
CKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVHIVSREAEAAEAEEPWGDEAREGRR
RGPRRESKPEEPPPPKKPALDKGPGSGQSAGSGPPRKTSGTVSGTARGTEVSSAAQAPAP
AASPPPEGPVLTFQSEKMKGMKELLVATKINSSAIKLQLTAQSQVQMKKQKVSTPSDYTL
SFLKRQRKGL
NT seq 1833 nt   +upstreamnt  +downstreamnt
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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