Homo sapiens (human): 4221
Help
Entry
4221 CDS
T01001
Symbol
MEN1, MEAI, SCG2
Name
(RefSeq) menin 1
KO
K14970
menin
Organism
hsa
Homo sapiens (human)
Pathway
hsa04934
Cushing syndrome
hsa05202
Transcriptional misregulation in cancer
Network
nt06360
Cushing syndrome
Element
N00290
Mutation-inactivated MEN1 to transcription
Disease
H00033
Adrenal carcinoma
H00034
Carcinoid
H00045
Pancreatic neuroendocrine tumor
H00246
Primary hyperparathyroidism
H00247
Multiple endocrine neoplasia syndrome
H01102
Pituitary adenomas
H01431
Cushing syndrome
H01522
Zollinger-Ellison syndrome
H01667
Medulloblastoma
H02049
Bilateral macronodular adrenal hyperplasia
Drug target
Icovamenib:
D12727
Revumenib (
DG03279
):
D12728
D12729
<US>
Ziftomenib:
D12419
Brite
KEGG Orthology (KO) [BR:
hsa00001
]
09160 Human Diseases
09161 Cancer: overview
05202 Transcriptional misregulation in cancer
4221 (MEN1)
09167 Endocrine and metabolic disease
04934 Cushing syndrome
4221 (MEN1)
09180 Brite Hierarchies
09182 Protein families: genetic information processing
03036 Chromosome and associated proteins [BR:
hsa03036
]
4221 (MEN1)
Chromosome and associated proteins [BR:
hsa03036
]
Eukaryotic type
Histone modification proteins
HMT complexes
MLL-HCF complex
4221 (MEN1)
BRITE hierarchy
SSDB
Ortholog
Paralog
Gene cluster
GFIT
Motif
Pfam:
Menin
Motif
Other DBs
NCBI-GeneID:
4221
NCBI-ProteinID:
NP_570711
OMIM:
613733
HGNC:
7010
Ensembl:
ENSG00000133895
UniProt:
O00255
Structure
PDB
PDBj
LinkDB
All DBs
Position
11:complement(64803516..64811294)
Genome browser
AA seq
610 aa
AA seq
DB search
MGLKAAQKTLFPLRSIDDVVRLFAAELGREEPDLVLLSLVLGFVEHFLAVNRVIPTNVPE
LTFQPSPAPDPPGGLTYFPVADLSIIAALYARFTAQIRGAVDLSLYPREGGVSSRELVKK
VSDVIWNSLSRSYFKDRAHIQSLFSFITGTKLDSSGVAFAVVGACQALGLRDVHLALSED
HAWVVFGPNGEQTAEVTWHGKGNEDRRGQTVNAGVAERSWLYLKGSYMRCDRKMEVAFMV
CAINPSIDLHTDSLELLQLQQKLLWLLYDLGHLERYPMALGNLADLEELEPTPGRPDPLT
LYHKGIASAKTYYRDEHIYPYMYLAGYHCRNRNVREALQAWADTATVIQDYNYCREDEEI
YKEFFEVANDVIPNLLKEAASLLEAGEERPGEQSQGTQSQGSALQDPECFAHLLRFYDGI
CKWEEGSPTPVLHVGWATFLVQSLGRFEGQVRQKVRIVSREAEAAEAEEPWGEEAREGRR
RGPRRESKPEEPPPPKKPALDKGLGTGQGAVSGPPRKPPGTVAGTARGPEGGSTAQVPAP
TASPPPEGPVLTFQSEKMKGMKELLVATKINSSAIKLQLTAQSQVQMKKQKVSTPSDYTL
SFLKRQRKGL
NT seq
1833 nt
NT seq
+upstream
nt +downstream
nt
atggggctgaaggccgcccagaagacgctgttcccgctgcgctccatcgacgacgtggtg
cgcctgtttgctgccgagctgggccgagaggagccggacctggtgctcctttccttggtg
ctgggcttcgtggagcattttctggctgtcaaccgcgtcatccctaccaacgttcccgag
ctcaccttccagcccagccccgcccccgacccgcctggcggcctcacctactttcccgtg
gccgacctgtctatcatcgccgccctctatgcccgcttcaccgcccagatccgaggcgcc
gtcgacctgtccctctatcctcgagaagggggtgtctccagccgtgagctggtgaagaag
gtctccgatgtcatatggaacagcctcagccgctcctacttcaaggatcgggcccacatc
cagtccctcttcagcttcatcacaggcaccaaattggacagctccggtgtggcctttgct
gtggttggggcctgccaggccctgggtctccgggatgtccacctcgccctgtctgaggat
catgcctgggtagtgtttgggcccaatggggagcagacagctgaggtcacctggcacggc
aagggcaacgaggaccgcaggggccagacagtcaatgccggtgtggctgagcggagctgg
ctgtacctgaaaggatcatacatgcgctgtgaccgcaagatggaggtggcgttcatggtg
tgtgccatcaacccttccattgacctgcacaccgactcgctggagcttctgcagctgcag
cagaagctgctctggctgctctatgacctgggacatctggaaaggtaccccatggcctta
gggaacctggcagatctagaggagctggagcccacccctggccggccagacccactcacc
ctctaccacaagggcattgcctcagccaagacctactatcgggatgaacacatctacccc
tacatgtacctggctggctaccactgtcgcaaccgcaatgtgcgggaagccctgcaggcc
tgggcggacacggccactgtcatccaggactacaactactgccgggaagacgaggagatc
tacaaggagttctttgaagtagccaatgatgtcatccccaacctgctgaaggaggcagcc
agcttgctggaggcgggcgaggagcggccgggggagcaaagccagggcacccagagccaa
ggttccgccctccaggaccctgagtgcttcgcccacctgctgcgattctacgacggcatc
tgcaaatgggaggagggcagtcccacgcctgtgctgcatgtgggctgggccacctttctt
gtgcagtccctaggccgttttgagggacaggtgcggcagaaggtgcgcatagtgagccga
gaggccgaggcggccgaggccgaggagccgtggggcgaggaagcccgggaaggccggcgg
cggggcccacggcgggagtccaagccagaggagcccccgccgcccaagaagccagcactg
gacaagggcctgggcaccggccagggtgcagtgtcaggacccccccggaagcctcctggg
actgtcgctggcacagcccgaggccctgaaggtggcagcacggctcaggtgccagcaccc
acagcatcaccaccgccggagggtccagtgctcactttccagagtgagaagatgaagggc
atgaaggagctgctggtggccaccaagatcaactcgagcgccatcaagctgcaactcacg
gcacagtcgcaagtgcagatgaagaagcagaaagtgtccacccctagtgactacactctg
tctttcctcaagcggcagcgcaaaggcctctga
DBGET
integrated database retrieval system