Genes in panel

Fetal anomalies

Gene: SGCD

Red List (low evidence)

SGCD (sarcoglycan delta)
EnsemblGeneIds (GRCh38): ENSG00000170624
EnsemblGeneIds (GRCh37): ENSG00000170624
OMIM: 601411, Gene2Phenotype
SGCD is in 9 panels

0 reviews

History Filter Activity

9 Mar 2026, Gel status: 1

Created, Added New Source, Set mode of inheritance

Arina Puzriakova (Genomics England Curator)

gene: SGCD was added gene: SGCD was added to Fetal anomalies. Sources: Expert Review Red Mode of inheritance for gene: SGCD was set to BIALLELIC, autosomal or pseudoautosomal