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Results for the Protein: P14543
251757450

NID1_HUMAN RecName: Full=Nidogen-1; Short=NID-1; AltName: Full=Entactin; Flags: Precursor

Known Diseases associated with this Protein:
  VARIANT OF UNKNOWN SIGNIFICANCE
1
14
1
8
6
Tips:
 The Domains on the Default View are decided by the Domain's E-Value.

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Default View:

NIDO - smart00539
NIDO - pfam06119
EGF_CA - cd00054
EGF - smart00181
EGF - cd00053
EGF - pfam00008
G2F - smart00682
G2F - pfam07474
nidG2 - cd00255
EGF_CA - pfam07645
EGF_CA - smart00179
TY - cd00191
Thyroglobulin_1 - pfam00086
TY - smart00211
LY - smart00135
Ldl_recept_b - pfam00058


Swiss-Prot Protein: P14543
Identical to: NP_002499
   Default View:








Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
EGFcd000532.8e-06389426
nidG2cd002553e-140429660
EGFcd000532.6e-05671709
EGF_CAcd000542.1e-11710751
EGFcd000531.2e-06713751
EGF_CAcd000544.3e-07758801
EGFcd000538.8e-06761801
EGF_CAcd000548e-16802840
EGFcd000532.9e-12805840
TYcd001912e-32848919
EGFpfam000080.00015390424
EGFpfam000082.4e-06672707
EGFpfam000080.00065714748
Thyroglobulin_1pfam000861.3e-32849919
Ldl_recept_bpfam000582.9e-109901029
Ldl_recept_bpfam000582e-1110331072
Ldl_recept_bpfam000586.7e-1010761117
NIDOsmart005391.2e-64106270
NIDOpfam061193.8e-41176268
EGFsmart001814.8e-06389426
G2Fsmart006829.1e-142427666
G2Fpfam074741.8e-121428626
EGFsmart001811.7e-05671709
EGF_CApfam076453.6e-09710750
EGF_CAsmart001791.6e-12710751
EGFsmart001811.3e-06713751
EGFsmart001814.8e-06761801
EGF_CApfam076454.4e-09802839
EGF_CAsmart001792.2e-15802840
EGFsmart001812.6e-11805840
TYsmart002119.8e-24875921
LYsmart001354.7e-069701012
LYsmart001351.6e-1710131055
LYsmart001352.6e-1510561100
LYsmart001350.000111011141
EGFsmart001810.0002312111244

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs16833183 Polymorphismp.ARG302HISN/A
dbSNPrs34406281 Polymorphismp.ARG335HISN/A
Swiss-ProtVAR_055763Polymorphismp.ARG387HISN/A
dbSNPrs2071529 Polymorphismp.ARG31LEUN/A
dbSNPrs3213190 Polymorphismp.GLN1246ARGN/A
Swiss-ProtVAR_021904Polymorphismp.GLN669ARGN/A
dbSNPrs3738531 Polymorphismp.GLN807HISN/A
dbSNPrs78916782 Polymorphismp.GLY504ARGN/A
Swiss-ProtVAR_055765Polymorphismp.LEU1163VALN/A
Swiss-ProtVAR_055764Polymorphismp.LYS970GLUN/A
Swiss-ProtVAR_035835Polymorphismp.PHE1036SERN/A
Swiss-ProtVAR_058123Polymorphismp.SER60ARGN/A
dbSNPrs6662744 Polymorphismp.THR1226ILEN/A
dbSNPrs10733133 Polymorphismp.VAL246ILEN/A
OMIM131390.0001 Diseasep.GLN388TERVARIANT OF UNKNOWN SIGNIFICANCE



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