Homo sapiens (human): 4256 Help 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) BRITE hierarchy SSDB OrthologParalogGene clusterGFIT Other DBs NCBI-GeneID:  4256 NCBI-ProteinID:  NP_000891 OMIM:  154870 HGNC:  7060 Ensembl:  ENSG00000111341 UniProt:  P08493 LinkDB All DBs Position 12:complement(14880864..14885854) Genome browser AA seq 103 aa AA seqDB search MKSLILLAILAALAVVTLCYESHESMESYELNPFINRRNANTFISPQQRWRAKVQERIRE RSKPVHELNREACDDYRLCERYAMVYGYNAAYNRYFRKRRGTK NT seq 312 nt NT seq  +upstreamnt  +downstreamnt atgaagagcctgatccttcttgccatcctggccgccttagcggtagtaactttgtgttat gaatcacatgaaagcatggaatcttatgaacttaatcccttcattaacaggagaaatgca aataccttcatatcccctcagcagagatggagagctaaagtccaagagaggatccgagaa cgctctaagcctgtccacgagctcaatagggaagcctgtgatgactacagactttgcgaa cgctacgccatggtttatggatacaatgctgcctataatcgctacttcaggaagcgccga gggaccaaatga

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