SLC4A7

solute carrier family 4 member 7
OMIM: 603353, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Red SLC4A7 in Genomic imprinting


Version 0.149

review MONOALLELIC, autosomal or pseudoautosomal, maternally imprinted (paternal allele expressed)
Sources
  • Literature
Red SLC4A7 in Monogenic hearing loss

Level 3: Non-syndromic hearing loss
Level 2: Hearing and ear disorders
Version 4.36
Latest signed off version: v4.0 (22 Mar 2023)

Component of the following Super Panels:

  • Paediatric disorders
  • review Not set
    Sources
    • Expert