The Microbe is a multi-speciality diagnostic laboratory established by a group of women entrepreneurs under the leadership of Dr Sharayu Gaikwad and Ms Vinita Dhoot. It provides a wide spectrum of diagnostic tests encompassing biochemistry, microbiology, cytopathology, histopathology, immunology, etc., with reliable and highly accurate reports. We believe in open communication and are available with a willing ear for report discussion.

The Microbe Lab

Gene analysis  APC

Gene analysis Â TTC7A

Gene analysis ABCA12 (harlequin ichthyosis)

Gene analysis Achondroplasia FGFR3 G380R common mutation

Gene analysis Alexander disease (GFAP)

Gene analysis Alpha-1 antitrypsin deficiency - SERPINA1

Gene analysis alpha-mannosidosis - Lysosomal storage disorder -

Gene analysis AlstrÃ¶m syndrome - ALMS1

Gene analysis Androgen receptor (AR)

Gene analysis Ataxia-telangiectasia (ATM)

Gene analysis ATRX

Gene analysis Brown Vialettoâ€“Van Laere syndrome

Gene analysis C8orf37 gene

Gene analysis Canavan disease (ASPA)

Gene analysis Cantu syndrome (ABCC9) gene

Gene analysis Carney complex (PRKAR1A)

Gene analysis Chediak-Higashi syndrome (LYST)

Gene analysis Cohen's syndrome (VPS13B)

Gene analysis Congenital adrenal hyperplasia CYP21A2 (21-0H) by NGS

Gene analysis Congenital adrenal hyperplasia CYP21A2 (21-0H) by

Gene analysis Cystic fibrosis (CFTR)-Whole gene

Gene analysis DOCK8 (Hyper IgE Syndrome) gene

Gene analysis DPYD whole  (for 5 FU toxicity evaluation)

Gene analysis Dravet syndrome (SCN1A)

Gene Analysis DRPLA Autosomal dominant Ataxia Blood

Gene analysis Duchenne Muscular Dystrophy (DMD) by NGS

Gene analysis Fabry disease (GLA)

Gene analysis Factor VII deficiency (F7)

Gene analysis Fanconi bickel syndrome (SLC2A2)

Gene analysis Farber lipogranulomatosis - ASAH1 -

Gene analysis Fraser syndrome genes

Gene analysis fucosidosis - Lysosomal storage disorder - FUCA1

Gene analysis Galactosialidosis - Lysosomal storage disorder - CTSA

Gene analysis GLB1 (GM1 gangliosidosis;

Gene analysis GLUT1 deficiency (SLC2A1)

Gene analysis Haemophilia A (F8)

Gene analysis Haemophilia B (F9)

Gene analysis Hereditary fructose intolerance - ALDOB gene

Gene analysis Hyperargininemia (ARG1)

Gene analysis Krabbe disease (GALC)

Gene analysis lysosomal acid lipase deficiency (LIPA gene)

Gene analysis Lysosomal storage disorder  screen, mini

Gene analysis Marfans syndrome (FBN1)

Gene analysis McArdle disease (PYGM)

Gene analysis Menkes disease (ATP7A)

Gene analysis Mondini defect (SLC26A4)

Gene analysis MYD88  gene L265P mutation

Gene analysis Neurofibromatosis type 1 (NF1)

Gene analysis Neurofibromatosis type 2 (NF2)

Gene analysis Pallister Hall syndrome (GLI3)

Gene analysis Phenylketonuria (PAH)

Gene analysis PMP22

Gene analysis Polycystic LiverDisease (Congenital cystic disease of Liver) PRKCSH, SEC63 -

Gene analysis Pompe disease (GAA)

Gene analysis Pulmonary alveolar microlithiasis (SLC34A2)

Gene analysis RANBP2

Gene analysis RAS extended profiling

G0142 Gene analysis RB1

Gene analysis RBC membrane disorders and Enzymopathies

Gene analysis Sialidosis - lysosomal storage disorder -  NEU1

Gene analysis Sjogren-Larsson syndrome (ALDH3A2)

Gene analysis SLC20A2 gene

Gene analysis Smith-Lemli-Opitz syndrome (DHCR7)

Gene analysis STK11

Gene analysis Tay-Sachs disease (HEXA)

Gene analysis TSC1

Gene analysis TSC1 & TSC2

Gene analysis Tyrosinemia

Gene analysis Von Willebrand disease (VWF)

Gene analysis WAS (Wiskott Aldrich Syndrome)Â .â€‹

Gene analysis Wilson disease (ATP7B)

Gene analysis Xanthinuria (XDH)

Gene deletion EP300 (Rubinstein-Taybi syndrome)

Gene deletion Rubinstein-Taybi syndrome - CREBBP gene

Gene Panel 4H syndrome

Gene Panel Aicardi-Goutieres syndrome

Gene Panel Alagille syndrome

Gene Panel Alport syndrome

Gene Panel Aplastic anemia

Gene Panel Arthrogryposis & congenital myasthenic syndrome

Gene Panel Bardet-Biedl syndrome

Gene Panel Bartter syndrome

Gene Panel Benign infantile epilepsy

Gene Panel Cancer hotspot

Gene Panel Cardiac channelopathy

Gene Panel Cardiomyopathy

Gene Panel Cataract (congenital/developmental)

Gene Panel Charcot-Marie-Tooth and sensory neuropathies

Gene Panel Ciliopathy

Gene Panel Citrullinemia

Gene Panel Clinical exom

Gene Panel Cockayne syndrome

Gene Panel Comprehensive Neurology

Gene Panel Congenital afibrinogenemia

Gene Panel Congenital dyserythropoietic anemia

Gene Panel Congenital Hyperpathyroidism -

Gene Panel Congenital hypopituitarism

Gene Panel Congenital neutropenia

Gene Panel Congenital stationary night blindness

Gene Panel Connective tissue disorder

NGS Gene Panel Test - Next Generation Sequencing Sequencing Gene Penel Test

NGS Gene Panel Test - Next Generation Sequencing Sequencing Gene Penel Test

About This Test

The Microbe Lab

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