NAA10

N(alpha)-acetyltransferase 10, NatA catalytic subunit
OMIM: 300013, Gene2Phenotype

11 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 11 panels
Green NAA10 in Anophthalmia_Microphthalmia_Coloboma Level 2: Ophthalmological disorders Version 1.50	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Phenotypes Microphthalmia, syndromic 1, MIM# 309800 Tags 5'UTR
Green NAA10 in Cerebral Palsy Level 2: Neurology and neurodevelopmental disorders Version 1.400	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 Literature Phenotypes Ogden syndrome MIM#300855
Green NAA10 in Mendeliome Version 1.3512	3 reviews	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 Microphthalmia, syndromic 1, MIM# 309800 Ogden syndrome MIM#300855 Tags 5'UTR
Green NAA10 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	5 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Victorian Clinical Genetics Services Australian Genomics Health Alliance Epilepsy Flagship Phenotypes NAA10-related syndrome MONDO:0100124
Green NAA10 in Callosome Level 2: Neurology and neurodevelopmental disorders Version 0.565	0 reviews	Unknown	Sources Victorian Clinical Genetics Services Expert Review Green
Green NAA10 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.410	2 reviews	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 Genetic Health Queensland Phenotypes Microphthalmia, syndromic 1, MIM# 309800 Ogden syndrome MIM#300855 Tags 5'UTR
Green NAA10 in Mackenzie's Mission_Reproductive Carrier Screening Level 2: Screening Version 0.110	0 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes N-terminal acetyltransferase deficiency, 300855 (3)
Red NAA10 in Additional findings_Paediatric Level 2: Screening Version 0.278	0 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Red BabySeq Category C gene Phenotypes N-terminal acetyltransferase deficiency
Green NAA10 in Fetal anomalies Version 1.465	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 Victorian Clinical Genetics Services Phenotypes Microphthalmia, syndromic 1, MIM# 309800 Ogden syndrome MIM#300855
Green NAA10 in Prepair 1000+ Level 2: Screening Version 2.14	1 review	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources Expert Review Green Mackenzie's Mission Phenotypes Ogden syndrome (MIM#300855) Syndromic microphthalmia 1 (MIM#309800)
Red NAA10 in Genomic newborn screening: BabyScreen+ Level 2: Screening Version 1.140	0 reviews	X-LINKED: hemizygous mutation in males, biallelic mutations in females	Sources BabySeq Category C gene Expert Review Red Phenotypes N-terminal acetyltransferase deficiency