KEGG   Homo sapiens (human): 4256
Entry
4256              CDS       T01001                                 
Symbol
MGP, GIG36, MGLAP, NTI
Name
(RefSeq) matrix Gla protein
  KO
K19481  matrix Gla protein
Organism
hsa  Homo sapiens (human)
Disease
H00500  Keutel syndrome
Brite
KEGG Orthology (KO) [BR:hsa00001]
 09190 Not Included in Pathway or Brite
  09193 Unclassified: signaling and cellular processes
   99995 Signaling proteins
    4256 (MGP)
SSDB
Other DBs
NCBI-GeneID: 4256
NCBI-ProteinID: NP_000891
OMIM: 154870
HGNC: 7060
Ensembl: ENSG00000111341
UniProt: P08493
Position
12:complement(14880864..14885854)
AA seq 103 aa
MKSLILLAILAALAVVTLCYESHESMESYELNPFINRRNANTFISPQQRWRAKVQERIRE
RSKPVHELNREACDDYRLCERYAMVYGYNAAYNRYFRKRRGTK
NT seq 312 nt   +upstreamnt  +downstreamnt
atgaagagcctgatccttcttgccatcctggccgccttagcggtagtaactttgtgttat
gaatcacatgaaagcatggaatcttatgaacttaatcccttcattaacaggagaaatgca
aataccttcatatcccctcagcagagatggagagctaaagtccaagagaggatccgagaa
cgctctaagcctgtccacgagctcaatagggaagcctgtgatgactacagactttgcgaa
cgctacgccatggtttatggatacaatgctgcctataatcgctacttcaggaagcgccga
gggaccaaatga

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