KEGG   ORTHOLOGY: K23328
Entry
K23328                      KO                                     
Symbol
DMP1
Name
dentin matrix acidic phosphoprotein 1
Pathway
map04512  ECM-receptor interaction
Disease
H00214  Hypophosphatemic rickets
H02139  Autosomal recessive hypophosphatemic rickets
Brite
KEGG Orthology (KO) [BR:ko00001]
 09130 Environmental Information Processing
  09133 Signaling molecules and interaction
   04512 ECM-receptor interaction
    K23328  DMP1; dentin matrix acidic phosphoprotein 1
Other DBs
GO: 0050840 0005178
Genes
HSA: 1758(DMP1)
PTR: 741526(DMP1)
PPS: 100991698(DMP1)
GGO: 101135619(DMP1)
PON: 100458882(DMP1)
NLE: 100580509(DMP1)
MCC: 701692(DMP1)
MCF: 102134200(DMP1)
CSAB: 103235938(DMP1)
CATY: 105576758(DMP1)
PANU: 101012466(DMP1)
TGE: 112625087(DMP1)
RRO: 104677955(DMP1)
RBB: 108526195(DMP1)
TFN: 117086344(DMP1)
PTEH: 111530885(DMP1)
CJC: 100414727(DMP1)
SBQ: 101052205(DMP1)
CSYR: 103273164(DMP1)
MMUR: 105876377(DMP1)
OGA: 100958070(DMP1)
MMU: 13406(Dmp1)
MCAL: 110295287(Dmp1)
MPAH: 110330959(Dmp1)
RNO: 25312(Dmp1)
MCOC: 116070750(Dmp1)
MUN: 110543552(Dmp1)
CGE: 100773494(Dmp1)
PLEU: 114691859(Dmp1)
NGI: 103748959(Dmp1)
HGL: 101725040(Dmp1)
CPOC: 100732102(Dmp1)
CCAN: 109678030(Dmp1)
DORD: 105995915(Dmp1)
DSP: 122097842(Dmp1)
NCAR: 124994009
OCU: 100345183(DMP1)
OPI: 101522063(DMP1)
TUP: 102488601(DMP1)
CFA: 487849(DMP1)
VVP: 112919613(DMP1)
VLG: 121493720(DMP1)
AML: 100481808(DMP1)
UMR: 103676963(DMP1)
UAH: 113263035(DMP1)
UAR: 123788284(DMP1)
ELK: 111157634
LLV: 125094254
MPUF: 101673681(DMP1)
ORO: 101363161(DMP1)
EJU: 114220072(DMP1)
ZCA: 113924082(DMP1)
MLX: 118010351(DMP1)
FCA: 101095652(DMP1)
PYU: 121032870(DMP1)
PBG: 122478675(DMP1)
PTG: 102952963(DMP1)
PPAD: 109276206(DMP1)
AJU: 106970778(DMP1)
HHV: 120226944(DMP1)
BTA: 281118(DMP1)
BOM: 102264744(DMP1)
BIU: 109560186(DMP1)
BBUB: 102399071(DMP1)
CHX: 102188028(DMP1)
OAS: 101123558(DMP1)
ODA: 120861552(DMP1)
CCAD: 122428380(DMP1)
SSC: 399688(DMP1)
CFR: 102504701(DMP1)
CBAI: 105077711(DMP1)
CDK: 105091577(DMP1)
VPC: 102537601(DMP1)
BACU: 103006218(DMP1)
LVE: 103080269(DMP1)
OOR: 101271738(DMP1)
DLE: 111179048(DMP1)
PCAD: 102984932(DMP1)
PSIU: 116754605(DMP1)
ECB: 100063014(DMP1)
EPZ: 103565308(DMP1)
EAI: 106831949(DMP1)
MYB: 102257218(DMP1)
MYD: 102762901(DMP1)
MMYO: 118654478(DMP1)
MLF: 102442311(DMP1)
MNA: 107537111(DMP1)
PKL: 118728562(DMP1)
HAI: 109396342(DMP1)
DRO: 112317873(DMP1)
SHON: 118987071(DMP1)
AJM: 119052675(DMP1)
PDIC: 114493381(DMP1)
PHAS: 123806924(DMP1)
MMF: 118618443(DMP1)
RFQ: 117022036(DMP1)
PALE: 102889142(DMP1)
PGIG: 120587975(DMP1)
PVP: 105289574(DMP1)
RAY: 107518919(DMP1)
MJV: 108401266(DMP1)
TOD: 119261119(DMP1)
SARA: 101546308(DMP1)
LAV: 100670815(DMP1)
TMU: 101341297
DNM: 101417897(DMP1)
MDO: 100016758(DMP1)
GAS: 123252223(DMP1)
SHR: 100924946
PCW: 110209648(DMP1)
OAA: 100085657(DMP1)
GGA: 404539(DMP1)
PCOC: 116231053(DMP1)
MGP: 100541753(DMP1)
CJO: 107313363(DMP1)
NMEL: 110398549(DMP1)
APLA: 101792557(DMP1)
ACYG: 106041859(DMP1)
AFUL: 116488613(DMP1)
TGU: 105759186
LSR: 110468519(DMP1)
SCAN: 103826299
PMOA: 120496064(DMP1)
OTC: 121339842
PRUF: 121360238
GFR: 102040084(DMP1)
FAB: 101808724(DMP1)
PHI: 102102446(DMP1)
PMAJ: 107202792(DMP1)
CCAE: 111928881
CCW: 104697337
ETL: 114057754
ZAB: 102070591(DMP1)
FPG: 101919692(DMP1)
FCH: 102056681
CLV: 102092264
EGZ: 104127338(DMP1)
NNI: 104015025(DMP1)
ACUN: 113479580
TALA: 116962846
PADL: 103919907
ACHC: 115346442
AAM: 106496652(DMP1)
AROW: 112965631(DMP1)
NPD: 112948957(DMP1)
DNE: 112984730
ASN: 102378760(DMP1)
AMJ: 106739175(DMP1)
PSS: 102454852(DMP1)
CMY: 102937292(DMP1)
CPIC: 101951321(DMP1)
TST: 117877843(DMP1)
CABI: 116836564(DMP1)
MRV: 120406114(DMP1)
ACS: 103278921(dmp1)
SUND: 121931732(DMP1)
PBI: 103067966(DMP1)
PMUR: 107290432(DMP1)
TSR: 106546653(DMP1)
PGUT: 117678937(DMP1)
VKO: 123022634
ZVI: 118084548(DMP1)
 » show all
Reference
PMID:9177774
  Authors
Hirst KL, Simmons D, Feng J, Aplin H, Dixon MJ, MacDougall M
  Title
Elucidation of the sequence and the genomic organization of the human dentin matrix acidic phosphoprotein 1 (DMP1) gene: exclusion of the locus from a causative role in the pathogenesis of dentinogenesis imperfecta type II.
  Journal
Genomics 42:38-45 (1997)
DOI:10.1006/geno.1997.4700
  Sequence
[hsa:1758]
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