GRXCR1

glutaredoxin and cysteine rich domain containing 1
OMIM: 613283, ClinGen, DECIPHER

4 panels

Panel Reviews Mode of inheritance Details
4 panels

Green GRXCR1 in Mendeliome


Version 1.3795

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 25, MIM# 613285

Green GRXCR1 in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.304

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • Melbourne Genomics Health Alliance Deafness Flagship
  • Victorian Clinical Genetics Services
Phenotypes
  • Deafness, autosomal recessive 25, MIM# 613285

Green GRXCR1 in Additional findings_Paediatric


Level 2: Screening
Version 0.278

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BabySeq Category C gene
Phenotypes
  • Deafness, autosomal recessive 25, MIM# 613285

Green GRXCR1 in Genomic newborn screening: BabyScreen+


Level 2: Screening
Version 1.141

1 review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Green
  • BabySeq Category C gene
Phenotypes
  • Deafness, autosomal recessive 25, MIM# 613285
Tags
  • deafness