Meckel syndrome 3

Summary
Synonym
  • MKS3
  • Meckel-Gruber syndrome, type 3
Definition
A Meckel syndrome that has_material_basis_in an autosomal recessive mutation of the TMEM67 gene on chromosome 8q22.1.
Super Class
Meckel syndrome
Disease Ontology
DOID:0070117
Mondo Disease Ontology
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
91147 TMEM67 transmembrane protein 67
Displaying 1 entry
Gene ID Gene Symbol Description Source
329795 Tmem67 transmembrane protein 67

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 v4.1.0

Last updated: December 9, 2024