COLEC10

collectin subfamily member 10
OMIM: 607620, Gene2Phenotype

6 panels

Panel Reviews Mode of inheritance Details
6 panels

Green COLEC10 in Blepharophimosis


Level 2: Ophthalmological disorders
Version 1.1

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Expert Review
Phenotypes
  • 3MC syndrome 3, MIM# 248340

Green COLEC10 in Mendeliome


Version 1.1891

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • 3MC syndrome 3, MONDO:0009554
  • 3MC syndrome 3, OMIM:248340

Red COLEC10 in Intellectual disability syndromic and non-syndromic


Level 2: Neurology and neurodevelopmental disorders
Version 0.6063

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
  • Genetic Health Queensland
Phenotypes
  • 3MC syndrome 3, MIM# 248340

Red COLEC10 in Skeletal dysplasia

Level 3: Skeletal dysplasias
Level 2: Skeletal disorders
Version 0.285

review Not set
Sources
  • Expert Review Green
  • NHS GMS
  • Victorian Clinical Genetics Services
Phenotypes
  • 3MC syndrome 3 -248340

Green COLEC10 in Clefting disorders

Level 3: Dysmorphic disorders
Level 2: Dysmorphic and congenital abnormality syndromes
Version 0.252

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
Phenotypes
  • 3MC SYNDROME 3
  • 3MC3

Green COLEC10 in Fetal anomalies


Version 1.255

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Genomics England PanelApp
  • Genetic Health Queensland
Phenotypes
  • 3MC syndrome 3, MONDO:0009554
  • 3MC syndrome 3, OMIM:248340