KEGG   Homo sapiens (human): 4212
Entry
4212              CDS       T01001                                 
Symbol
MEIS2, CPCMR, HsT18361, MRG1
Name
(RefSeq) Meis homeobox 2
  KO
K16670  homeobox protein Meis2
Organism
hsa  Homo sapiens (human)
Disease
H02394  Cleft palate, cardiac defects, and mental retardation
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    4212 (MEIS2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain TALE
    4212 (MEIS2)
SSDB
Motif
Pfam: Meis_PKNOX_N Homeobox_KN Homeodomain
Other DBs
NCBI-GeneID: 4212
NCBI-ProteinID: NP_733775
OMIM: 601740
HGNC: 7001
Ensembl: ENSG00000134138
UniProt: O14770 B3KPD8
Structure
Position
15:complement(36889204..37101311)
AA seq 477 aa
MAQRYDELPHYGGMDGVGVPASMYGDPHAPRPIPPVHHLNHGPPLHATQHYGAHAPHPNV
MPASMGSAVNDALKRDKDAIYGHPLFPLLALVFEKCELATCTPREPGVAGGDVCSSDSFN
EDIAVFAKQVRAEKPLFSSNPELDNLMIQAIQVLRFHLLELEKVHELCDNFCHRYISCLK
GKMPIDLVIDERDGSSKSDHEELSGSSTNLADHNPSSWRDHDDATSTHSAGTPGPSSGGH
ASQSGDNSSEQGDGLDNSVASPGTGDDDDPDKDKKRQKKRGIFPKVATNIMRAWLFQHLT
HPYPSEEQKKQLAQDTGLTILQVNNWFINARRRIVQPMIDQSNRAGFLLDPSVSQGAAYS
PEGQPMGSFVLDGQQHMGIRPAGLQSMPGDYVSQGGPMGMSMAQPSYTPPQMTPHPTQLR
HGPPMHSYLPSHPHHPAMMMHGGPPTHPGMTMSAQSPTMLNSVDPNVGGQVMDIHAQ
NT seq 1434 nt   +upstreamnt  +downstreamnt
atggcgcaaaggtacgatgagctgccccattacggcgggatggacggagtaggggttccc
gcttccatgtacggagaccctcacgcgccgcggccgatccccccggttcaccacctgaac
cacgggccgccgctccacgccacacagcactacggcgcgcacgccccgcaccccaatgtc
atgccggccagtatgggatccgctgtcaacgacgccttgaagcgggacaaggacgcgatc
tatgggcacccgttgtttcctctgttagctctggtctttgagaagtgcgagctggcgacc
tgcactccccgggaacctggagtggctggcggagacgtctgctcctccgactccttcaac
gaggacatcgcggtcttcgccaagcaggttcgcgccgaaaagccacttttttcctcaaat
ccagagctggacaatttgatgatacaagcaatacaagtactaaggtttcatcttttggag
ttagaaaaggtccacgaactgtgcgataacttctgccaccgatacattagctgtttgaag
gggaaaatgcccatcgacctcgtcattgatgaaagagacggcagctccaagtcagatcat
gaagaactttcaggctcctccacaaatctcgctgaccataacccttcttcttggcgagac
cacgatgatgcaacctcaacccactcagcaggcaccccagggccctccagtgggggccat
gcttcccagagcggagacaacagcagtgagcaaggggatggtttagacaacagtgtagct
tcacctggtacaggtgacgatgatgatccggataaggacaaaaaacgccagaagaaaaga
ggcattttccccaaagtagcaacaaatatcatgagagcatggctcttccagcatctcaca
catccgtacccttccgaagagcagaagaaacagttagcgcaagacacaggacttacaatt
ctccaagtaaacaactggtttattaatgccagaagaagaatagtacagcccatgattgac
cagtcaaatcgagcaggttttcttcttgatccttcagtgagccaaggagcagcatatagt
ccagagggtcagcccatggggagctttgtgttggatggtcagcaacacatggggatccgg
cctgcaggtttgcagagcatgccaggggactacgtttctcagggtggtcctatgggaatg
agtatggcacagccaagttacactcctccccagatgaccccacaccctactcaattaaga
catggacccccaatgcattcatatttgccaagccatccccaccacccagccatgatgatg
cacggaggaccccctacccaccctggaatgactatgtcagcacagagccccacaatgtta
aattctgtagatcccaatgttggcggacaggttatggacattcatgcccaatag

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (14)   
   KEGG ORTHOLOGY (1)   
   RefGene (3)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   RIKEN BRC-DNA (5)   
   OC (1)   
Protein sequence (11)   
   UniProt (2)   
   SWISS-PROT (1)   
   RefSeq(pep) (8)   
DNA sequence (58)   
   RefSeq(nuc) (10)   
   GenBank (24)   
   EMBL (24)   
3D Structure (4)   
   PDB (4)   
Protein domain (3)   
   Pfam (3)   
All databases (96)   

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