Glyco-Disease Genes Database (GDGDB)

GDGDB is a database of glycan-related diseases and their responsible genes.

Source Last Updated
Glyco-Disease Genes Database (GDGDB) January 25, 2017
Displaying entries 76 - 100 of 152 in total
Concept UI Disease Name Gene Symbol Disease Name Aliases ▼ Disease Type UniProt ID Disease IDs
CON00356 RFT1-CDG RFT1
  • CDG-In
  • Congenital disorder of glycosylation, type In
  • RFT1 (flippase) deficiency
Congenital Disorders of Glycosylation (CDGs) Q96AA3
CON00355 DOLK-CDG TMEM15
  • CDG-Im
  • Congenital disorder of glycosylation, type Im
  • DK1 deficiency
  • DK1-CDG
  • Dolichol kinase deficiency
Congenital Disorders of Glycosylation (CDGs) Q9UPQ8
CON00353 ALG1-CDG ALG1
  • CDG-Ik
  • Congenital disorder of glycosylation, type Ik
Congenital Disorders of Glycosylation (CDGs) Q9BT22
CON00352 DPAGT1-CDG DPAGT1
  • CDG-Ij
  • Congenital disorder of glycosylation, type Ij
Congenital Disorders of Glycosylation (CDGs) Q9H3H5
CON00351 ALG2-CDG ALG2
  • CDG-Ii
  • Congenital disorder of glycosylation, type Ii
Congenital Disorders of Glycosylation (CDGs) Q9H553
CON00350 ALG8-CDG ALG8
  • CDG-Ih
  • Congenital disorder of glycosylation, type Ih
Congenital Disorders of Glycosylation (CDGs) Q9BVK2
CON00349 ALG12-CDG ALG12
  • CDG-Ig
  • Congenital disorder of glycosylation, type Ig
Congenital Disorders of Glycosylation (CDGs) Q9BV10
CON00348 MPDU1-CDG MPDU1
  • CDG-If
  • Congenital disorder of glycosylation, type If
Congenital Disorders of Glycosylation (CDGs) O75352
CON00347 DPM1-CDG DPM1
  • CDG-Ie
  • Congenital disorder of glycosylation, type Ie
Congenital Disorders of Glycosylation (CDGs) O60762
CON00346 ALG3-CDG ALG3
  • CDG-Id
  • Congenital disorder of glycosylation, type Id
Congenital Disorders of Glycosylation (CDGs) Q92685
CON00345 ALG6-CDG ALG6
  • CDG-Ic
  • Congenital disorder of glycosylation, type Ic
Congenital Disorders of Glycosylation (CDGs) Q9Y672
CON00344 MPI-CDG MPI
  • CDG-Ib
  • Congenital disorder of glycosylation, type Ib
  • Mannosephosphate isomerase deficiency
  • Protein-losing enteropathy-hepatic fibrosis syndrome
  • Saguenay-Lac Saint-Jean syndrome
Congenital Disorders of Glycosylation (CDGs) P34949
CON00343 PMM2-CDG PMM2
  • CDG-Ia
  • Congenital disorder of glycosylation, type Ia
  • Jaeken syndrome
  • Phosphomannomutase 2 deficiency
Congenital Disorders of Glycosylation (CDGs) O15305
CON00354 ALG9-CDG ALG9
  • CDG-IL
  • Congenital disorder of glycosylation, type IL
Congenital Disorders of Glycosylation (CDGs) Q9H6U8
CON00626 TMEM165-CDG TMEM165
  • CDG-IIk
  • Congenital Disorder of Glycosylation, Type IIk
Congenital Disorders of Glycosylation (CDGs) Q9HC07
CON00367 COG4-CDG COG4
  • CDG-IIj
  • Congenital disorder of glycosylation, type IIj
Congenital Disorders of Glycosylation (CDGs) Q9H9E3
CON00366 COG5-CDG COG5
  • CDG-IIi
  • Congenital disorder of glycosylation, type IIi
Congenital Disorders of Glycosylation (CDGs) Q9UP83
CON00365 COG8-CDG COG8
  • CDG-IIh
  • COG8 deficiency
  • Congenital disorder of glycosylation, type IIh
Congenital Disorders of Glycosylation (CDGs) Q96MW5
CON00364 COG1-CDG COG1
  • CDG-IIg
  • CDGII/COG1 Cerebrocostomandibular-like syndrome
  • COG1 deficiency
  • Congenital disorder of glycosylation, type IIg
Congenital Disorders of Glycosylation (CDGs) Q8WTW3
CON00363 SLC35A1-CDG SLC35A1
  • CDG-IIf
  • Congenital disorder of glycosylation, type IIf
Congenital Disorders of Glycosylation (CDGs) P78382
CON00362 COG7-CDG COG7
  • CDG-IIe
  • Congenital disorder of glycosylation, type IIe
Congenital Disorders of Glycosylation (CDGs) P83436
CON00361 B4GALT1-CDG B4GALT1
  • CDG-IId
  • Congenital disorder of glycosylation, type IId
Congenital Disorders of Glycosylation (CDGs) P15291
CON00360 SLC35C1-CDG SLC35C1
  • CDG-IIc
  • Congenital disorder of glycosylation, type IIc
  • Leukocyte adhesion deficiency, type 2
  • Rambam Hasharon syndrome
Congenital Disorders of Glycosylation (CDGs) Q96A29
CON00359 GCS1-CDG GCS1
  • CDG-IIb
  • Congenital disorder of glycosylation, type IIb
  • MOGS-CDG
Congenital Disorders of Glycosylation (CDGs) Q13724
CON00358 MGAT2-CDG MGAT2
  • CDG-IIa
  • Congenital disorder of glycosylation, type IIa
Congenital Disorders of Glycosylation (CDGs) Q10469

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