PAN2

PAN2 poly(A) specific ribonuclease subunit
OMIM: 617447, ClinGen, DECIPHER

5 panels

Panel	Reviews	Mode of inheritance	Details
Filter panels 5 panels
Green PAN2 in Congenital anomalies of the kidney and urinary tract (CAKUT) Syndromic Level 2: Renal and urinary tract disorders Version 0.160 Component of the following Super Panels: Congenital abnormalities of the kidneys and urinary tract (CAKUT)_SuperPanel Kidneyome_SuperPanel	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Expert Review Green Phenotypes Developmental delay with variable cardiac and renal congenital anomalies and dysmoprhic facies, MIM# 621384
Green PAN2 in Congenital Heart Defect Level 2: Cardiovascular disorders Version 0.510	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Developmental delay with variable cardiac and renal congenital anomalies and dysmoprhic facies, MIM# 621384
Green PAN2 in Mendeliome Version 1.3795	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Developmental delay with variable cardiac and renal congenital anomalies and dysmoprhic facies, MIM# 621384
Green PAN2 in Intellectual disability syndromic and non-syndromic Level 2: Neurology and neurodevelopmental disorders Version 1.497	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Developmental delay with variable cardiac and renal congenital anomalies and dysmoprhic facies, MIM# 621384
Green PAN2 in Fetal anomalies Version 1.481	2 reviews	BIALLELIC, autosomal or pseudoautosomal	Sources Expert Review Green Literature Phenotypes Developmental delay with variable cardiac and renal congenital anomalies and dysmoprhic facies, MIM# 621384