SATB1

SATB homeobox 1
OMIM: 602075, Gene2Phenotype

4 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 4 panels
Green SATB1 in Mendeliome Version 1.3520	4 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Kohlschutter-Tonz syndrome-like, MIM# 619229 Developmental delay with dysmorphic facies and dental anomalies, MIM# 619228 Neurodevelopmental disorder intellectual disability epilepsy microcephaly
Green SATB1 in Genetic Epilepsy Level 2: Neurology and neurodevelopmental disorders Version 1.267 Component of the following Super Panels: Progressive Neurological Conditions	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Literature Phenotypes Kohlschutter-Tonz syndrome-like, MIM# 619229 Neurodevelopmental disorder Intellectual disability Epilepsy Microcephaly Regression
Green SATB1 in Regression Level 2: Neurology and neurodevelopmental disorders Version 0.594	2 reviews	MONOALLELIC, autosomal or pseudoautosomal, imprinted status unknown	Sources Expert Review Green Literature Phenotypes Kohlschutter-Tonz syndrome-like, MIM# 619229 Neurodevelopmental disorder regression
Green SATB1 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.411	3 reviews	MONOALLELIC, autosomal or pseudoautosomal, NOT imprinted	Sources Expert Review Green Literature Phenotypes Kohlschutter-Tonz syndrome-like, MIM# 619229 Developmental delay with dysmorphic facies and dental anomalies, MIM# 619228 Neurodevelopmental disorder intellectual disability epilepsy microcephaly