SLC4A11

solute carrier family 4 member 11
OMIM: 610206, Gene2Phenotype

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green SLC4A11 in Corneal Dystrophy Level 2: Ophthalmological disorders Version 1.13	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268 Corneal endothelial dystrophy and perceptive deafness, MIM# 217400 Corneal endothelial dystrophy, autosomal recessive, MIM# 217700
Green SLC4A11 in Mendeliome Version 1.3512	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268 Corneal endothelial dystrophy and perceptive deafness, MIM# 217400 Corneal endothelial dystrophy, autosomal recessive, MIM# 217700
Green SLC4A11 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.238	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes Corneal endothelial dystrophy and perceptive deafness, MIM# 217400
Green SLC4A11 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes Corneal endothelial dystrophy
Red SLC4A11 in Prepair 1000+ Level 2: Screening Version 2.14	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Literature Phenotypes Corneal dystrophy, Fuchs endothelial, 4, MIM# 613268 Corneal endothelial dystrophy and perceptive deafness, MIM# 217400 Corneal endothelial dystrophy, autosomal recessive, MIM# 217700
Red SLC4A11 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	1 review	BOTH monoallelic and biallelic, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes Corneal endothelial dystrophy and perceptive deafness, MIM# 217400