3MC syndrome 3

Summary
Definition
A 3MC syndrome that has_material_basis_in a compound heterozygous mutation in the COLEC10 gene on chromosome 8q24.
Super Class
3MC syndrome
External Links
Disease Ontology
DOID:0060577
Mondo Disease Ontology
OMIM
Related Genes
Displaying all 3 entries
Gene ID Gene Symbol Description Source
5648 MASP1 MBL associated serine protease 1
10584 COLEC10 collectin subfamily member 10
78989 COLEC11 collectin subfamily member 11
Related Glycoprotein
Displaying all 2 entries
UniProt ID Protein Name Source
P48740 Mannan-binding lectin serine protease 1
Q9Y6Z7 Collectin-10
The Human Phenotype Ontology
Displaying entries 11 - 20 of 45 in total
HPO ID HPO Term
HP:0000593 Abnormal anterior chamber morphology
HP:0001249 Intellectual disability
HP:0001363 Craniosynostosis
HP:0001537 Umbilical hernia
HP:0001540 Diastasis recti
HP:0002265 Large fleshy ears
HP:0002553 Highly arched eyebrow
HP:0002558 Supernumerary nipple
HP:0002650 Scoliosis
HP:0002714 Downturned corners of mouth
Displaying all 3 entries
Gene ID Gene Symbol Description
10584 COLEC10 collectin subfamily member 10
5648 MASP1 MBL associated serine protease 1
78989 COLEC11 collectin subfamily member 11

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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