atransferrinemia

Summary
Synonym
  • familial hypotransferrinemia
Definition
A metal metabolism disorder that is characterized by transferrin deficiency, microcytic anemia, and iron loading, and has_material_basis_in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the structural gene for transferrin (TF) on chromosome 3q22.
Super Class
autosomal recessive disease metal metabolism disorder
External Links
Disease Ontology
DOID:0050649
Mondo Disease Ontology
NCI Thesaurus
ORDO
OMIM
GARD
MGI genotype (from TogoID)
WikiPathways (from TogoID)
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
7018 TF transferrin
Displaying 1 entry
Gene ID Gene Symbol Description Source
22041 Trf transferrin
Displaying 1 entry
Gene ID Gene Symbol Description Source
24825 Tf transferrin
Displaying 1 entry
Gene ID Gene Symbol Description Source
39435 Tsf2 Transferrin 2

About Release Notes Help Feedback

International Collaboration

GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

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


Logo License Policies Site Map

Contact: support@glycosmos.org

This work is licensed under Creative Commons Attribution 4.0 International


GlyCosmos Portal v4.0.0

Last updated: August 19, 2024