KEGG   Homo sapiens (human): 265
Entry
265               CDS       T01001                                 
Symbol
AMELX, AI1E, AIH1, ALGN, AMG, AMGL, AMGX
Name
(RefSeq) amelogenin X-linked
  KO
K23443  amelogenin
Organism
hsa  Homo sapiens (human)
Disease
H00615  Amelogenesis imperfecta
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99992 Structural proteins
    265 (AMELX)
SSDB
Motif
Pfam: Amelogenin
Other DBs
NCBI-GeneID: 265
NCBI-ProteinID: NP_001133
OMIM: 300391
HGNC: 461
Ensembl: ENSG00000125363
UniProt: Q99217
Position
X:11293413..11309588
AA seq 191 aa
MGTWILFACLLGAAFAMPLPPHPGHPGYINFSYEVLTPLKWYQSIRPPYPSYGYEPMGGW
LHHQIIPVLSQQHPPTHTLQPHHHIPVVPAQQPVIPQQPMMPVPGQHSMTPIQHHQPNLP
PPAQQPYQPQPVQPQPHQPMQPQPPVHPMQPLPPQPPLPPMFPMQPLPPMLPDLTLEAWP
STDKTKREEVD
NT seq 576 nt   +upstreamnt  +downstreamnt
atggggacctggattttatttgcctgcctcctgggagcagcttttgccatgcctctacca
cctcatcctgggcaccctggttatatcaacttcagctatgaggtgcttacccctttgaag
tggtaccagagcataaggccaccgtacccttcctatggttacgagcccatgggtggatgg
ctgcaccaccaaatcatccccgtgctgtcccaacagcaccccccgactcacaccctgcag
cctcatcaccacatcccagtggtgccagctcagcagcccgtgatcccccagcaaccaatg
atgcccgttcctggccaacactccatgactccaatccaacaccaccagccaaacctccct
ccgcccgcccagcagccctaccagccccagcctgttcagccacagcctcaccagcccatg
cagccccagccacctgtgcaccccatgcagcccctgccgccacagccacctctgcctccg
atgttccccatgcagcccctgcctcccatgcttcctgatctgactctggaagcttggcca
tcaacagacaagaccaagcgggaggaagtggattaa

  All links  
Ontology (1)   
   KEGG BRITE (1)   
Disease (3)   
   KEGG DISEASE (1)   
   OMIM (2)   
Genome (1)   
   KEGG GENOME (1)   
Gene (11)   
   KEGG ORTHOLOGY (1)   
   RefGene (5)   
   NCBI-PROTEINID (1)   
   NCBI-Gene (1)   
   HGNC (1)   
   Ensembl (1)   
   OC (1)   
Protein sequence (7)   
   UniProt (1)   
   SWISS-PROT (1)   
   RefSeq(pep) (5)   
DNA sequence (15)   
   RefSeq(nuc) (5)   
   GenBank (5)   
   EMBL (5)   
Protein domain (1)   
   Pfam (1)   
All databases (39)   

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