CUL7

cullin 7
OMIM: 609577, ClinGen, DECIPHER

9 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 9 panels
Green CUL7 in Skeletal Dysplasia_Fetal Level 2: Skeletal disorders Version 0.246	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Expert list Literature Phenotypes 3-M syndrome 1 - MIM#273750 Yakut short stature syndrome
Green CUL7 in Mendeliome Version 1.4601	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes 3-M syndrome 1, MIM# 273750 Yakut short stature syndrome
Green CUL7 in Skeletal dysplasia Level 3: Skeletal dysplasias Level 2: Skeletal disorders Version 0.417	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green NHS GMS Phenotypes 3-M syndrome 1, MIM# 273750 Yakut short stature syndrome
Green CUL7 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.111	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes 3-M syndrome 1, 273750 (3)
Green CUL7 in Additional findings_Paediatric Level 2: Screening Version 0.280	0 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources BabySeq Category A gene Expert Review Green Phenotypes 3-M syndrome
Green CUL7 in Growth failure Version 1.99	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes 3-M syndrome 1, MIM# 273750 Yakut short stature syndrome
Green CUL7 in Fetal anomalies Version 1.544	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Genomics England PanelApp Phenotypes 3-M syndrome 1, MIM# 273750 Yakut short stature syndrome
Green CUL7 in Prepair 1000+ Level 2: Screening Version 2.15	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Mackenzie's Mission Phenotypes 3-M syndrome 1, MIM#273750
Red CUL7 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.147	1 review	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Red BabySeq Category A gene Phenotypes 3-M syndrome 1, MIM# 273750