KEGG   Homo sapiens (human): 84504
Entry
84504             CDS       T01001                                 
Symbol
NKX6-2, GTX, NKX6.2, NKX6B, SPAX8
Name
(RefSeq) NK6 homeobox 2
  KO
K09350  homeobox protein Nkx-6.2
Organism
hsa  Homo sapiens (human)
Disease
H01351  Spastic ataxia
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09180 Brite Hierarchies
  09182 Protein families: genetic information processing
   03000 Transcription factors [BR:hsa03000]
    84504 (NKX6-2)
Transcription factors [BR:hsa03000]
 Eukaryotic type
  Helix-turn-helix
   Homeo domain ANTP: NKL
    84504 (NKX6-2)
SSDB
Motif
Pfam: Homeodomain Homeobox_KN PKK ABC_trans_N
Other DBs
NCBI-GeneID: 84504
NCBI-ProteinID: NP_796374
OMIM: 605955
HGNC: 19321
Ensembl: ENSG00000148826
UniProt: Q9C056
Position
10:complement(132783181..132786147)
AA seq 277 aa
MDTNRPGAFVLSSAPLAALHNMAEMKTSLFPYALQGPAGFKAPALGGLGAQLPLGTPHGI
SDILGRPVGAAGGGLLGGLPRLNGLASSAGVYFGPAAAVARGYPKPLAELPGRPPIFWPG
VVQGAPWRDPRLAGPAPAGGVLDKDGKKKHSRPTFSGQQIFALEKTFEQTKYLAGPERAR
LAYSLGMTESQVKVWFQNRRTKWRKRHAVEMASAKKKQDSDAEKLKVGGSDAEDDDEYNR
PLDPNSDDEKITRLLKKHKPSNLALVSPCGGGAGDAL
NT seq 834 nt   +upstreamnt  +downstreamnt
atggacactaaccgcccgggcgcgttcgtgctgagcagtgccccgctggccgcgctgcac
aacatggccgagatgaagacgtcgctgttcccctacgcgctgcagggtccggccggcttc
aaggcgcccgcgctggggggcctgggcgcgcagctcccgctcgggaccccgcacggcatc
agcgacatcctgggccggcccgtgggcgcggcgggcgggggcctcctgggggggctgccc
cggctcaacgggctcgcgtcgtccgccggcgtttacttcgggcccgcggccgctgtggcg
cgcggctaccccaagcccctggccgagctgccggggcgcccgcccatcttctggcccggc
gtggtgcagggcgcgccctggagggacccgcgtctggctggcccggccccggccggcggc
gtcctggacaaggacgggaagaagaagcactcgcgcccgaccttctcgggccagcagatc
ttcgcgctggagaaaaccttcgagcagaccaagtacctggcgggcccggagcgcgcgcgt
ctcgcctactcgctgggcatgaccgagagccaggtgaaggtctggttccagaaccgccgg
accaagtggcgcaagcggcacgcggtggagatggcgtcggccaagaagaagcaggactcg
gacgccgagaagctgaaggtgggcggctcggacgcggaggacgacgacgaatacaaccgg
cccctggaccccaactcggacgacgagaagatcacgcggctgctcaagaagcacaaaccc
tcgaacttggcgctggtcagcccgtgcggcggcggcgcgggggacgccttgtga

  All links  
Ontology (2)   
   KEGG BRITE (2)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (7)   
   KEGG ORTHOLOGY (1)   
   RefGene (1)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (4)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (2)   
DNA sequence (8)   
   RefSeq(nuc) (2)   
   GenBank (3)   
   EMBL (3)   
Protein domain (4)   
   Pfam (4)   
All databases (29)   

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