TAAR1

trace amine associated receptor 1
OMIM: 609333, Gene2Phenotype

1 panel

Panel Reviews Mode of inheritance Details
1 panel
Red TAAR1 in Fetal anomalies


Level 2: Fetal (including NIPD)
Version 6.140
Latest signed off version: v6.0 (30 Apr 2025)

review BIALLELIC, autosomal or pseudoautosomal
Sources
  • Expert Review Red
Phenotypes
  • Cerebellar vermis hypoplasia, cystic kidneys, polydactyly