IGSF1

immunoglobulin superfamily member 1
OMIM: 300137, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green IGSF1 in Mendeliome Version 2.631	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Hypothyroidism, central, and testicular enlargement, MIM# 300888
Green IGSF1 in Pituitary hormone deficiency Level 3: Pituitary disorders Level 2: Endocrine disorders Version 1.21	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Genomics England PanelApp Phenotypes Hypothyroidism, central, and testicular enlargement, MIM# 300888
Green IGSF1 in Congenital hypothyroidism Level 3: Thyroid disorders Level 2: Endocrine disorders Version 1.7	1 review	X-LINKED: hemizygous mutation in males, monoallelic mutations in females may cause disease (may be less severe, later onset than males)	Sources Expert Review Green Genomics England PanelApp Phenotypes Hypothyroidism, central, and testicular enlargement, MIM# 300888
Red IGSF1 in Fetal anomalies Version 2.89	2 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red Genomics England PanelApp Phenotypes Hypothyroidism, central, and testicular enlargement MIM#300888
Green IGSF1 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 2.13	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green BabySeq Category A gene Phenotypes Hypothyroidism, central, and testicular enlargement, MIM# 300888 Tags treatable endocrine