1. Genes and Genomic Entities
  2. SLC30A7

SLC30A7

solute carrier family 30 member 7
OMIM: 611149, Gene2Phenotype

2 panels

Panel Reviews Mode of inheritance Details
2 panels
Amber SLC30A7 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 7.7
Latest signed off version: v7.0 (6 May 2026)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Amber
  • NHS GMS
Phenotypes
  • Ziegler-Huang syndrome, OMIM:620501
Red SLC30A7 in DDG2P


Version 7.1
Latest signed off version: v7.0 (6 May 2026)

Component of the following Super Panels:

  • Paediatric disorders

    		•  review MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown
    Sources
    • Expert Review Red
    • DD-Gene2Phenotype
    Phenotypes
    • SLC30A7-associated Joubert syndrome