rs121908340
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
|
14709599 |
2004 |
rs121908340
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
|
14973782 |
2004 |
rs121908340
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
|
14973778 |
2004 |
rs121908340
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
|
26931382 |
2016 |
rs151173406
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
|
14709599 |
2004 |
rs151173406
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
|
14973782 |
2004 |
rs151173406
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
|
14973778 |
2004 |
rs151173406
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
|
26931382 |
2016 |
rs267606651
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
|
14973778 |
2004 |
rs267606651
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
|
26931382 |
2016 |
rs267606651
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
|
14709599 |
2004 |
rs267606651
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
|
14973782 |
2004 |
rs28939378
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.800 |
GeneticVariation |
UNIPROT |
|
|
|
rs1057520122
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
|
26931382 |
2016 |
rs1057520122
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
|
14973778 |
2004 |
rs1057520122
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
|
14709599 |
2004 |
rs1057520122
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
|
14973782 |
2004 |
rs1180515976
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs1299775990
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deficiency of GDP-Man:GlcNAc2-PP-dolichol mannosyltransferase causes congenital disorder of glycosylation type Ik.
|
14973778 |
2004 |
rs1299775990
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Deficiency of the first mannosylation step in the N-glycosylation pathway causes congenital disorder of glycosylation type Ik.
|
14709599 |
2004 |
rs1299775990
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
ALG1-CDG: Clinical and Molecular Characterization of 39 Unreported Patients.
|
26931382 |
2016 |
rs1299775990
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
Congenital disorder of glycosylation type Ik (CDG-Ik): a defect of mannosyltransferase I.
|
14973782 |
2004 |
rs16835020
|
ALG1;EEF2KMT
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs192564717
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|
rs200605408
|
Entrez Id: |
56052 |
Gene Symbol: |
ALG1 |
ALG1
|
Congenital disorder of glycosylation type 1K
|
|
0.700 |
GeneticVariation |
UNIPROT |
|
|
|