|
|
|
|
| | Tips: The Domains on the Default View are decided by the Domain's E-Value. Clicking a check box will display or hide the correlated domain. To view the Gene page, either click on the link to the left or the blue bar above the Protein's graphic. |
---|
Default View:
| |
---|
Domains found on the Protein Table of Mutations found on the ProteinSource ↕ | Mut_ID ↕ | Class ↕ | HGVS ↕ | Disease ↕ |
---|
Swiss-Prot | VAR_042063 | Polymorphism | p.ARG378CYS | N/A | Swiss-Prot | VAR_042066 | Polymorphism | p.ARG1031GLN | N/A | Swiss-Prot | VAR_042068 | Polymorphism | p.ARG1075GLN | N/A | dbSNP | rs115824945 | Polymorphism | p.ARG1320GLN | N/A | dbSNP | rs1130379 | Polymorphism | p.ARG1146HIS | N/A | dbSNP | rs307821 | Polymorphism | p.ARG1324LEU | N/A | Swiss-Prot | VAR_018413 | Disease | p.ARG1041PRO | Lymphedema, hereditary, 1A (LMPH1A) | dbSNP | rs34221241 | Polymorphism | p.ASN149ASP | N/A | dbSNP | rs35874891 | Polymorphism | p.ASN527SER | N/A | Swiss-Prot | VAR_042067 | Polymorphism | p.ASP1049ASN | N/A | Swiss-Prot | VAR_018409 | Disease | p.GLY857ARG | Lymphedema, hereditary, 1A (LMPH1A) | Swiss-Prot | VAR_018412 | Disease | p.HIS1035ARG | Lymphedema, hereditary, 1A (LMPH1A) | dbSNP | rs448012 | Polymorphism | p.HIS890GLN | N/A | Swiss-Prot | VAR_042064 | Polymorphism | p.HIS868TYR | N/A | Swiss-Prot | VAR_018414 | Disease | p.LEU1044PRO | Lymphedema, hereditary, 1A (LMPH1A) | Swiss-Prot | VAR_018415 | Disease | p.PRO1114LEU | Lymphedema, hereditary, 1A (LMPH1A) | Swiss-Prot | VAR_018416 | Disease | p.PRO1137SER | Hemangioma, capillary infantile (HCI) | Swiss-Prot | VAR_018408 | Polymorphism | p.PRO641SER | N/A | Swiss-Prot | VAR_018411 | Disease | p.PRO954SER | Hemangioma, capillary infantile (HCI) | dbSNP | rs307826 | Polymorphism | p.THR494ALA | N/A | Swiss-Prot | VAR_042065 | Polymorphism | p.THR1010ILE | N/A | OMIM | 136352.0012 | Disease | p.ALA855THR | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0003 | Disease | p.ARG1041PRO | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0010 | Disease | p.GLU1106LYS | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0002 | Disease | p.GLY857ARG | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0006 | Disease | p.HIS1035ARG | LYMPHEDEMA, HEREDITARY, I | OMIM | 136352.0009 | Disease | p.ILE1086THR | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0004 | Disease | p.LEU1044PRO | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0005 | Disease | p.PRO1114LEU | LYMPHEDEMA, HEREDITARY, IA | OMIM | 136352.0007 | Disease | p.PRO954SER | HEMANGIOMA, CAPILLARY INFANTILE, SOMATIC | OMIM | 136352.0008 | Disease | p.VAL878MET | LYMPHEDEMA, HEREDITARY, IA |
Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.
DMDM_info@umbc.edu | 1000 Hilltop Circle, Baltimore, MD
21250 | Department of Biological Sciences | Phone: 410-455-2258 |
|