Jalili syndrome

Summary
Synonym
  • Cone rod dystrophy-amelogenesis imperfecta syndrome
  • cone-rod dystrophy and amelogenesis imperfecta
Definition
A syndrome characterized by amelogenesis imperfecta and cone-rod retinal dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in CNNM4 on chromosome 2q11.2.
Super Class
autosomal recessive disease syndrome
External Links
Disease Ontology
DOID:0111404
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
GARD
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
26504 CNNM4 cyclin and CBS domain divalent metal cation transport mediator 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
94220 Cnnm4 cyclin M4
Displaying 1 entry
Gene ID Gene Symbol Description Source
363216 Cnnm4 cyclin and CBS domain divalent metal cation transport mediator 4
Displaying 1 entry
Gene ID Gene Symbol Description Source
5740320 uex unextended
Displaying 1 entry
Gene ID Gene Symbol Description Source Organism
100036645 cnnm4 cyclin and CBS domain divalent metal cation transport mediator 4 Xenopus tropicalis (tropical clawed frog)
Displaying all 2 entries
Gene ID Gene Symbol Description Source
178499 cnnm-1 Metal transporter cnnm-1
180591 cnnm-3 Metal transporter cnnm-3

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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: August 19, 2024