congenital disorder of glycosylation type IIn

Summary
Synonym
  • CDG IIn
  • CDG syndrome type IIn
  • CDG2N
  • CDGIIdn
  • Carbohydrate deficient glycoprotein syndrome type IIn
  • Congenital disorder of glycosylation type 2n
  • SLC39A8-CDG
Definition
A congenital disorder of glycosylation type II that has_material_basis_in an autosomal recessive mutation of the SLC39A8 gene on chromosome 4q24.
Super Class
autosomal recessive disease congenital disorder of glycosylation type II
Disease Ontology
DOID:0070266
Mondo Disease Ontology
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
64116 SLC39A8 solute carrier family 39 member 8
Displaying 1 entry
Gene ID Gene Symbol Description Source
67547 Slc39a8 solute carrier family 39 (metal ion transporter), member 8
Displaying 1 entry
Gene ID Gene Symbol Description Source
295455 Slc39a8 solute carrier family 39 member 8
The Human Phenotype Ontology
Displaying entries 31 - 40 of 48 in total
HPO ID HPO Term
HP:0008277 Abnormal blood zinc concentration
HP:0008314 Decreased activity of mitochondrial complex II
HP:0008347 Decreased activity of mitochondrial complex IV
HP:0008873 Disproportionate short-limb short stature
HP:0009826 Limb undergrowth
HP:0010621 Cutaneous syndactyly of toes
HP:0012301 Type II transferrin isoform profile
HP:0012368 Flat face
HP:0012736 Profound global developmental delay
HP:0000007 Autosomal recessive inheritance
Displaying 1 entry
Gene ID Gene Symbol Description
64116 SLC39A8 solute carrier family 39 member 8

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024