FOXI1

forkhead box I1
OMIM: 601093, ClinGen, DECIPHER

6 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 6 panels
Green FOXI1 in Mendeliome Version 1.2302	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes autosomal recessive distal renal tubular acidosis MONDO:0018440
Green FOXI1 in Deafness_IsolatedAndComplex Level 2: Hearing and ear disorders Version 1.210	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes autosomal recessive distal renal tubular acidosis MONDO:0018440
Red FOXI1 in Deafness_Isolated Level 2: Hearing and ear disorders Version 1.67	3 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Victorian Clinical Genetics Services Melbourne Genomics Health Alliance Deafness Flagship Melbourne Genomics Health Alliance Deafness Flagship Victorian Clinical Genetics Services Phenotypes enlarged vestibular aqueduct syndrome MONDO:0023069
Green FOXI1 in Additional findings_Paediatric Level 2: Screening Version 0.278	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Phenotypes sensorineural deafness and distal renal tubular acidosis
Red FOXI1 in BabyScreen+ newborn screening Level 2: Screening Version 1.116	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red Expert list Phenotypes autosomal recessive distal renal tubular acidosis MONDO:0018440
Green FOXI1 in Renal Tubulopathies and related disorders Level 2: Renal and urinary tract disorders Version 1.17 Component of the following Super Panels: Kidneyome_SuperPanel	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Expert Review Green Literature Phenotypes autosomal recessive distal renal tubular acidosis MONDO:0018440