SPATC1L

spermatogenesis and centriole associated 1 like
OMIM: 612412, Gene2Phenotype

3 panels

Panel Reviews Mode of inheritance Details
3 panels

Amber SPATC1L in Mendeliome


Version 1.3098

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Hearing loss disorder, MONDO:0005365 SPATC1L-related

Amber SPATC1L in Deafness_IsolatedAndComplex


Level 2: Hearing and ear disorders
Version 1.222

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
Phenotypes
  • Hearing loss disorder, MONDO:0005365 SPATC1L-related

Amber SPATC1L in Deafness_Isolated


Level 2: Hearing and ear disorders
Version 1.74

review BOTH monoallelic and biallelic, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • Expert list
  • Expert list
Phenotypes
  • Deafness