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Results for the Protein: P11047
224471885

LAMC1_HUMAN RecName: Full=Laminin subunit gamma-1; AltName: Full=Laminin B2 chain; AltName: Full=Laminin-1 subunit gamma; AltName: Full=Laminin-10 subunit gamma; AltName: Full=Laminin-11 subunit gamma; AltName: Full=Laminin-2 subunit gamma; AltName: Full=Laminin-3 subunit gamma; AltName: Full=Laminin-4 subunit gamma; AltName: Full=Laminin-6 subunit gamma; AltName: Full=Laminin-7 subunit gamma; AltName: Full=Laminin-8 subunit gamma; AltName: Full=Laminin-9 subunit gamma; AltName: Full=S-laminin subunit gamma; Short=S-LAM gamma; Flags: Precursor

Known Diseases associated with this Protein:
  VARIANT OF UNKNOWN SIGNIFICANCE
1
6
1
5
1
Tips:
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Default View:

LamNT - smart00136
Laminin_N - pfam00055
EGF_Lam - cd00055
EGF_Lam - smart00180
Laminin_EGF - pfam00053
LamB - smart00281
Laminin_B - pfam00052


Swiss-Prot Protein: P11047
Identical to: NP_002284
   Default View:





Domains found on the Protein

Domain ↕CD Accession ↕E-Value ↕Start ↕End ↕
EGF_Lamcd000551.7e-13341396
EGF_Lamcd000553.7e-17397443
EGF_Lamcd000554.7e-20444493
EGF_Lamcd000554e-17723771
EGF_Lamcd000552.6e-09772826
EGF_Lamcd000552.1e-15827882
EGF_Lamcd000551.2e-16883933
EGF_Lamcd000555.8e-18934981
EGF_Lamcd000553.3e-149821029
Laminin_Npfam000554.2e-16550284
Laminin_EGFpfam000533.2e-10286339
Laminin_EGFpfam000534.5e-15342395
Laminin_EGFpfam000538.9e-18398442
Laminin_EGFpfam000539.4e-20445492
Laminin_Bpfam000525.3e-71558688
Laminin_EGFpfam000534.7e-16724770
Laminin_EGFpfam000532.4e-05773825
Laminin_EGFpfam000537.6e-16828881
Laminin_EGFpfam000531.4e-15884932
Laminin_EGFpfam000531.3e-16935980
Laminin_EGFpfam000534.9e-139831028
LamNTsmart001364.6e-15144284
EGF_Lamsmart001803.2e-14286339
EGF_Lamsmart001806.3e-13342395
EGF_Lamsmart001801.3e-15398442
EGF_Lamsmart001808.4e-20445492
LamBsmart002818.9e-49553678
EGF_Lamsmart001803.9e-17724770
EGF_Lamsmart001806.1e-07773825
EGF_Lamsmart001804e-13828881
EGF_Lamsmart001802.9e-15884932
EGF_Lamsmart001804.5e-16935980
EGF_Lamsmart001805.7e-139831028

Table of Mutations found on the Protein

Source ↕Mut_ID ↕Class ↕HGVS ↕Disease ↕
dbSNPrs20559 Polymorphismp.ARG1121GLNN/A
Swiss-ProtVAR_035821Polymorphismp.ARG1116HISN/A
dbSNPrs20557 Polymorphismp.ASN837LYSN/A
dbSNPrs2230157 Polymorphismp.GLU731LYSN/A
dbSNPrs20563 Polymorphismp.ILE458VALN/A
dbSNPrs20558 Polymorphismp.LEU888PRON/A
OMIM150290.0001 Diseasep.THR746METVARIANT OF UNKNOWN SIGNIFICANCE



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