Carrier Screening Gene Lists | Advanced 500 & Premium 787 | Cytogenomix® Malaysia

Expanded Carrier Screening Gene Lists

Complete lists of genes included in our Advanced 500 and Premium 787 panels

Advanced 500
447 Genes
Premium 787
620 Genes
Deletion/Duplication Detection: Both panels detect copy number variants (CNVs) ≥2 exons, providing comprehensive coverage beyond single nucleotide variants.
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Showing 100 of 620 genes
AR X-Linked Unknown
Gene Condition Inheritance Panel
AAAS Achalasia-addisonism-alacrima (Triple A) syndrome AR Advanced Premium
ABCA12 Congenital ichthyosis, ABCA12-related AR Advanced Premium
ABCA3 Surfactant metabolism dysfunction, pulmonary 3 AR Premium
ABCA4 Stargardt disease AR Advanced Premium
ABCB11 Progressive familial intrahepatic cholestasis AR Advanced Premium
ABCB4 Progressive familial intrahepatic cholestasis AR Advanced Premium
ABCC2 Dubin-Johnson syndrome AR Premium
ABCC6 Arterial calcification, generalized, of infancy, 2/Pseudoxanthoma elasticum AR Advanced Premium
ABCC8 Familial hyperinsulinism AR Advanced Premium
ABCD1 Adrenoleukodystrophy, X-linked XL Advanced Premium
ACAD9 Acyl-CoA dehydrogenase-9 (ACAD9) deficiency/ Mitochondrial Complex 1 Deficiency AR Advanced Premium
ACADM Medium-chain acyl-CoA dehydrogenase deficiency AR Advanced Premium
ACADS Acyl-CoA dehydrogenase, short-chain, deficiency of AR Advanced Premium
ACADSB 2-methylbutyrylglycinuria AR Advanced Premium
ACADVL Very long-chain acyl-CoA dehydrogenase deficiency AR Advanced Premium
ACAT1 Beta-ketothiolase deficiency AR Advanced Premium
ACE Renal tubular dysgenesis - ace AR Advanced Premium
ACOX1 Peroxisomal acyl-CoA oxidase deficiency AR Advanced Premium
ACSF3 Combined malonic and methylmalonic aciduria AR Advanced Premium
ADA Adenosine deaminase deficiency AR Advanced Premium
ADAMTS2 Ehlers-Danlos syndrome, dermatosparaxis type AR Advanced Premium
ADAMTSL4 Isolated ectopia lentis AR Premium
ADGRG1 Bilateral frontoparietal polymicrogyria AR Premium
ADGRV1 Usher syndrome, type IIIC AR Premium
ADK Adenosine kinase deficiency AR Advanced Premium
AGA Aspartylglucosaminuria AR Advanced Premium
AGL Glycogen storage disease type III AR Advanced Premium
AGPS Rhizomelic chondrodysplasia punctata, type 3 AR Advanced Premium
AGXT Primary hyperoxaluria type I AR Advanced Premium
AHCY Hypermethioninemia with deficiency of s-adenosylhomocysteine hydrolase AR Advanced Premium
AHI1 Joubert syndrome, AHI1-related AR Premium
AIPL1 Childhood-onset severe retinal dystrophy, AIPL1-related AR Premium
AIRE Autoimmune polyendocrinopathy syndrome type I AR Advanced Premium
ALDH3A2 Sjögren-Larsson syndrome AR Advanced Premium
ALDH7A1 Pyridoxine-dependent epilepsy AR Advanced Premium
ALDOB Hereditary fructose intolerance AR Advanced Premium
ALG1 Congenital disorder of glycosylation type Ik (ALG1) AR Premium
ALG13 ALG13-related conditions XL Premium
ALG6 Congenital disorder of glycosylation type Ic (ALG6) AR Advanced Premium
ALMS1 Alström syndrome AR Advanced Premium
ALPL Hypophosphatasia AR Advanced Premium
AMH Persistent Müllerian duct syndrome type 1 AR Advanced Premium
AMHR2 Persistent Müllerian duct syndrome type 2 AR Advanced Premium
AMN Megaloblastic anemia 1 AR Premium
AMT Glycine encephalopathy AR Advanced Premium
ANO10 Spinocerebellar ataxia 10 AR Premium
AP1S1 MEDNIK syndrome AR Advanced Premium
AQP2 Nephrogenic diabetes insipidus AR Advanced Premium
AR Androgen insensitivity syndrome XL Advanced Premium
ARG1 Arginase deficiency AR Advanced Premium
ARL6 ARL6-related disorders AR Premium
ARSA Metachromatic leukodystrophy AR Advanced Premium
ARSB Mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome) AR Advanced Premium
ARSE Chondrodysplasia punctata type 1, X-linked XL Premium
ARX X-linked intellectual disability, ARX-related XL Premium
ASL Argininosuccinate lyase deficiency AR Advanced Premium
ASNS Asparagine synthetase deficiency AR Advanced Premium
ASPA Canavan disease AR Advanced Premium
ASPM Autosomal recessive primary microcephaly AR Advanced Premium
ASS1 Citrullinemia AR Advanced Premium
ATM Ataxia-telangiectasia/Ataxia with isolated vitamin E deficiency AR Advanced Premium
ATP6V1B1 Renal tubular acidosis with deafness AR Advanced Premium
ATP7A Menkes disease XL Advanced Premium
ATP7B Wilson disease AR Advanced Premium
ATP8B1 Progressive familial intrahepatic cholestasis AR Advanced Premium
ATRX Alpha thalassemia X-linked intellectual disability syndrome XL Advanced Premium
AVPR2 Nephrogenic diabetes insipidus XL Premium
BBS1 Bardet-Biedl syndrome type 1 AR Advanced Premium
BBS10 Bardet-Biedl syndrome type 10 AR Advanced Premium
BBS12 Bardet-Biedl syndrome type 12 AR Advanced Premium
BBS2 Bardet-Biedl syndrome 2 / Retinitis pigmentosa 74 AR Advanced Premium
BBS4 Bardet-Biedl syndrome 4 AR Advanced Premium
BBS5 Bardet-Biedl syndrome 5 AR Premium
BBS7 Bardet-Biedl syndrome 7 AR Premium
BBS9 Bardet-Biedl syndrome 9 AR Advanced Premium
BCHE Pseudocholinesterase deficiency AR Advanced Premium
BCKDHA Maple syrup urine disease type Ia AR Advanced Premium
BCKDHB Maple syrup urine disease type Ib AR Advanced Premium
BCS1L Mitochondrial complex II deficiency AR Advanced Premium
BLM Bloom syndrome AR Advanced Premium
BLOC1S3 Hermansky-Pudlak syndrome 8 AR Premium
BLOC1S6 Hermansky-Pudlak syndrome 9 AR Premium
BMP1 Osteogenesis imperfecta, type XIII AR Premium
BRIP1 Fanconi anemia group J AR Advanced Premium
BSND Bartter syndrome, Type 4A AR Advanced Premium
BTD Biotinidase deficiency AR Advanced Premium
BTK X-linked agammaglobulinemia XL Advanced Premium
CAD Early Infantile Epileptic Encephalopathy 50 AR Premium
CANT1 Desbuquois dysplasia 1 AR Advanced Premium
CAPN3 Limb-girdle muscular dystrophy type 2A AR Advanced Premium
CASQ2 Catecholaminergic Polymorphic Ventricular Tachycardia, CASQ2-related AR Advanced Premium
CBS Homocystinuria due to cystathionine beta-synthase deficiency AR Advanced Premium
CC2D1A Autosomal recessive intellectual developmental disorder 3 AR Advanced Premium
CC2D2A Joubert syndrome 9 AR Premium
CCDC103 Primary ciliary dyskinesia, type 17 AR Premium
CCDC39 Primary ciliary dyskinesia, type 14 AR Premium
CCDC88C Congenital hydrocephalus AR Premium
CD3D Severe Combined Immunodeficiency AR Premium
CD3E Severe Combined Immunodeficiency AR Premium
CD40 Immunodeficiency with Hyper IgM syndrome AR Premium
Fragile X Syndrome (FMR1) - Both panels include full CGG trinucleotide repeat analysis of the FMR1 gene, detecting normal, intermediate, premutation, and full mutation alleles.
Inheritance Key: AR = Autosomal Recessive | XL = X-Linked | UK = Unknown/Complex