Official registry information on file with the National Plan and Provider Enumeration System.
STAR LABORATORY (NPI 1134439573) is a healthcare organization registered as a clinical medical laboratory in Piscataway, New Jersey and active in the NPI registry since October 2010. The organization holds an CLIA Accreditation certificate valid through October 1, 2027 and lists Sam Khawaja, Ceo, as its authorized official.
(1) A clinical laboratory is a facility for the biological, microbiological, serological, chemical, immunohematological, hematological, biophysical, cytological, pathological, or other examination of materials derived from the human body for the purpose of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, human beings. These examinations also include procedures to determine, measure, or otherwise describe the presence or absence of various substances or organisms in the body. Facilities only collecting or preparing specimens (or both) or only serving as a mailing service and not performing testing are not considered clinical laboratories. (2) Any facility that examines materials from the human body for purposes of providing information for the diagnosis, prevention, or treatment of any disease or impairment of, or the assessment of, the health of human beings. Typical divisions of a clinical laboratory include hematology, cytology, bacteriology, histology, biochemistry, medical toxicology, and serology.
Laboratory certificates issued under the Clinical Laboratory Improvement Amendments (CLIA) program, which sets federal quality standards for human laboratory testing in the United States. There is no official CMS crosswalk between CLIA and NPI numbers; these certificates are associated with this NPI by matching facility names, locations and phone numbers in the CMS CLIA registry.
CLIA data matches this NPI record on: ✓ Address✓ Name✓ Phone
This is a certificate that is issued to a laboratory on the basis of the laboratory's accreditation by an accreditation organization approved by CMS.
Areas of Expertise CMS Part B claims61
Services this provider delivered to Medicare fee-for-service patients, from the CMS Medicare utilization data. Higher counts generally reflect more experience with a service; care delivered outside Medicare is not included.
Gene analysis, specifically MUTS Homolog 6 (E. coli) full sequence analysis, is a test that examines your DNA to identify changes in the MUTS Homolog 6 gene. This information helps doctors understand and manage potential health concerns.
Gene analysis, specifically postmeiotic segregation increased 2 (s cerevisiae) full sequence analysis, is a scientific procedure. It involves studying your entire genetic code to identify any changes or differences that could be related to certain health conditions. This is done in a lab, using a sample provided by you.
3,239 services3,239 patients
Gene analysis (partner and localizer of brca2) full sequence analysis 81307
Gene analysis, specifically for the partner and localizer of BRCA2, involves examining your genetic code to identify any changes in this particular gene. This gene is significant in maintaining the health of your cells. The full sequence analysis means we look at every part of this gene to ensure it's working properly.
Gene analysis, specifically Janus Kinase 2 (JAK2) targeted sequence analysis, is a lab test that studies a specific gene in your body. It helps identify changes or mutations in the JAK2 gene, which can be linked to certain health conditions. This analysis is performed on a blood or bone marrow sample.
Gene analysis of the MPL proto-oncogene, thrombopoietin receptor, specifically sequence analysis of exon 10, is a procedure that studies a specific part of your DNA. It helps to identify any changes or mutations that may contribute to certain blood disorders.
2,407 services2,392 patients
Gene analysis (glucose-6-phosphatase, catalytic subunit) common variants 81250
Gene analysis of glucose-6-phosphatase, catalytic subunit, common variants involves studying specific genes related to glucose metabolism. This helps understand if you're at risk of certain metabolic disorders. It's a non-invasive procedure, involving a simple blood or saliva sample.
Gene analysis for cystic fibrosis involves examining the entire CFTR gene to identify any changes or mutations that could cause the disease. This can help in diagnosing and managing the condition effectively.
2,262 services2,262 patients
Gene analysis (glucose-6-phosphate dehydrogenase) full sequence analysis 81249
Gene analysis for glucose-6-phosphate dehydrogenase (G6PD) involves studying your DNA to check for changes in the G6PD gene. This gene controls an enzyme that helps red blood cells function properly. Anomalies can cause health issues like anemia.
Gene analysis for Bloom Syndrome involves studying the RECQ helicase-like gene. This gene is responsible for DNA repair. When it's not working properly, it can lead to Bloom Syndrome, a condition that increases the risk of developing various types of cancer.
2,229 services2,229 patients
Gene analysis (coagulation factor ix) full sequence analysis 81238
Gene analysis for coagulation factor IX is a process that examines your genes, specifically the one responsible for factor IX - a protein that helps blood clot. It can detect any changes or mutations in this gene, which could affect your body's ability to control bleeding.
2,223 services2,223 patients
Gene analysis (fanconi anemia, complementation group c) common variant 81242
Gene analysis for Fanconi Anemia, Complementation Group C, is a test that looks at your DNA to see if you have changes in a specific gene linked to this type of anemia. This can help determine if you have the condition or if you might pass it on to your children.
Gene analysis, specifically neurotrophic receptor tyrosine kinase 1 (NTRK1) translocation analysis, is a test that examines your genes for specific changes. These changes could potentially lead to certain health conditions. This analysis helps in providing personalized treatment plans.
Gene analysis, specifically neurotrophic receptor tyrosine kinase 2 (NTRK2) translocation analysis, is a test that studies alterations in your genes. This analysis helps identify changes in the NTRK2 gene, which can sometimes be linked to certain health conditions. It's a vital part of personalized medicine.
2,138 services2,123 patients
Gene analysis (huntingtin) for abnormal alleles 81271
Gene analysis for huntingtin examines your DNA to identify if you have abnormal versions of the huntingtin gene. These abnormal genes are associated with Huntington's disease, a nervous system disorder. This test helps in early detection and management.
Gene analysis for ataxin 8 opposite strand checks for unusual gene variants. This test helps identify genetic conditions that could affect your health. It involves analyzing your DNA, usually from a blood sample, to find these abnormal alleles.
2,097 services2,095 patients
Gene analysis (aspartoacylase) 81200
Gene analysis for aspartoacylase is a test that studies your DNA to check for mutations in the ASPA gene. This gene is responsible for producing an enzyme called aspartoacylase, which plays a crucial role in brain development and function. Any changes could lead to health issues.
2,097 services2,095 patients
Gene analysis (atropin 1) for abnormal alleles 81177
Gene analysis for Atropin 1 involves studying your DNA to identify any unusual genetic variations. This test helps in understanding your genetic makeup better, which can aid in diagnosing or predicting certain health conditions.
2,096 services2,094 patients
Gene analysis (survival of motor neuron 1, telomeric) of full sequence 81336
Gene analysis of the full sequence of Survival of Motor Neuron 1 (telomeric) is a test that examines your DNA to identify any changes in this specific gene. These changes could indicate conditions like Spinal Muscular Atrophy. It's a non-invasive procedure.
2,094 services2,092 patients
Gene analysis (fragile x syndrome, x-linked intellectual disability) for detection of abnormal alleles 81243
Gene analysis for Fragile X Mental Retardation involves studying your DNA to identify any abnormal changes or 'alleles'. This helps in detecting the presence of Fragile X syndrome, a genetic condition that can cause learning and behavioral challenges.
2,093 services2,091 patients
Gene analysis (ataxin 1) for abnormal alleles 81178
Gene analysis of ataxin 1 involves studying your DNA to identify any abnormal versions of the ataxin 1 gene. This gene is associated with certain neurological disorders. The test helps in early detection and management of these conditions.
2,091 services2,089 patients
Gene analysis (ataxin 3) for abnormal alleles 81180
Gene analysis for ataxin 3 helps identify abnormal alleles, or variations, in the ataxin 3 gene. This gene plays a role in neurological function. If abnormal, it may indicate conditions like Machado-Joseph disease. The process involves analyzing a blood sample.
2,091 services2,089 patients
Gene analysis (ataxin 10) for abnormal alleles 81183
Gene analysis for ataxin 10 involves examining your DNA to identify any abnormal versions of the ataxin 10 gene. These abnormalities could potentially cause certain health conditions. This test is non-invasive and helps in early detection and management of these conditions.
2,091 services2,089 patients
Gene analysis (ataxin 7) for abnormal alleles 81181
Gene analysis for ataxin 7 involves studying your DNA to identify any unusual changes in the ataxin 7 gene. These changes, known as abnormal alleles, can cause health conditions like spinocerebellar ataxia. The test helps in early detection and management.
2,090 services2,088 patients
Gene analysis (cystatin b) of full sequence 81189
Gene analysis of the full sequence of Cystatin B is a test that examines your DNA to identify any changes in the Cystatin B gene. This gene is linked to certain health conditions. The analysis helps in diagnosing and tailoring treatment plans.
Gene analysis for the protein phosphatase 2 regulatory subunit Bbeta checks for unusual variations in your genes. This helps to identify potential health issues related to these genes. It's a simple, non-invasive test using a blood or saliva sample.
2,090 services2,088 patients
Gene analysis (fragile x intellectual disability 2) for detection of abnormal alleles 81171
Gene analysis for Fragile X Mental Retardation 2 involves studying your genetic material to identify any unusual changes in a specific gene. This can help determine if you have a particular genetic condition, or if you might pass it on to your children.
2,089 services2,087 patients
Gene analysis (inhibitor of kappa light polypeptide gene enhancer in b-cells, kinase complex-associated protein) common variants 81260
Gene analysis for common variants in the IKBKAP gene helps understand your body's response to certain medications. This non-invasive test studies your DNA to identify variations in this gene, which can influence drug effectiveness and safety.
2,087 services2,085 patients
Gene analysis (ataxin 2) for abnormal alleles 81179
Gene analysis for ataxin 2 checks for alterations in the ATXN2 gene. This gene is responsible for producing a protein essential for normal cell functions. If abnormal, it may lead to certain neurological disorders. The test involves analyzing your DNA, typically obtained via a blood sample.
2,086 services2,084 patients
Gene analysis (tata box binding protein) for abnormal alleles 81344
Gene analysis for the TATA box binding protein checks for abnormal alleles or variations in your DNA. This analysis helps identify potential genetic conditions. It's done by examining a sample of your cells, typically obtained through a blood draw or a cheek swab.
2,085 services2,083 patients
Gene analysis (hexosaminidase a) common variants 81255
Gene analysis of Hexosaminidase A common variants is a test that examines your DNA for changes in the Hex A gene. This gene is responsible for making an enzyme that breaks down certain substances in the body. Changes in this gene can lead to health issues.
2,081 services2,081 patients
Gene analysis (poly[a] binding protein nuclear 1) for abnormal alleles 81312
Gene analysis for Poly(A) Binding Protein Nuclear 1 (PABPN1) checks for abnormal alleles or variations in your DNA. This test can help identify genetic disorders caused by these variations. It's a non-invasive procedure, involving a simple blood or saliva sample.
2,081 services2,079 patients
Gene analysis (glucosidase, beta, acid) common variants 81251
Gene analysis of common variants in the beta-glucosidase acid enzyme helps understand certain health conditions. This enzyme plays a key role in the body's metabolism. By studying its variants, doctors can better diagnose and treat metabolic disorders.
2,077 services2,077 patients
Gene analysis (peripheral myelin protein 22), full sequence analysis 81325
Gene analysis of peripheral myelin protein 22 involves studying the full sequence of this specific gene. This analysis helps identify any genetic variations that may lead to certain health conditions. It's a non-invasive test involving a simple blood draw or saliva sample.
2,073 services2,073 patients
Gene analysis (partner and localizer of brca2) targeted sequence analysis 81309
Gene analysis, specifically the partner and localizer of BRCA2 targeted sequence analysis, is a scientific procedure that studies specific parts of your DNA. It helps to identify if you have certain genetic changes that may increase your risk of developing specific health conditions.
2,064 services2,062 patients
Gene analysis (5, 10-methylenetetrahydrofolate reductase) common variants 81291
Gene analysis for 5,10-methylenetetrahydrofolate reductase (MTHFR) common variants is a test that looks at your DNA to identify any changes in the MTHFR gene. These changes can affect how your body processes certain vitamins, which could impact your overall health.
2,063 services2,061 patients
Gene analysis (frataxin) of full sequence 81286
Gene analysis of frataxin involves studying the entire sequence of the frataxin gene. This test helps identify any changes or mutations in the gene that may cause health issues, such as Friedreich's ataxia. It's a non-invasive procedure using a blood sample.
2,061 services2,059 patients
Gene analysis (hemochromatosis) common variants 81256
Gene analysis for hemochromatosis common variants is a test that checks for specific changes in your DNA. These changes could indicate a higher risk of developing hemochromatosis, a condition that causes your body to absorb too much iron from your diet.
2,054 services2,054 patients
Gene analysis panel for evaluation of genes associated with epilepsy 81419
A gene analysis panel for epilepsy evaluates specific genes linked to this condition. This test can help understand your epilepsy type and severity, potentially guiding treatment options. It involves a blood sample and lab analysis.
2,036 services2,034 patients
Gene analysis (adenomatous polyposis coli), full gene sequence 81201
Gene analysis of the adenomatous polyposis coli (APC) involves studying the entire sequence of the APC gene. This test helps identify mutations that could lead to conditions like familial adenomatous polyposis. The procedure is non-invasive and uses a blood sample.
1,334 services1,334 patients
Gene analysis (muts homolog 2, colon cancer, nonpolyposis type 1) full sequence analysis 81295
Gene analysis (MUTYH) full sequence analysis is a test that examines your DNA to identify any changes linked to nonpolyposis colon cancer type 1. This can help determine your risk of developing this type of cancer.
1,294 services1,294 patients
Gene analysis (breast cancer 1 and 2) of full sequence and analysis for duplication or deletion variants 81162
Gene analysis for breast cancer 1 and 2 involves studying your DNA to detect alterations that may increase your risk of developing certain health issues. This test analyzes the full sequence and checks for duplication or deletion variants.
449 services449 patients
Complete blood cell count (red cells, white blood cell, platelets), automated test and automated differential white blood cell count 85025
A Complete Blood Cell Count is a common test that measures various components of the blood, including red cells (carry oxygen), white cells (fight infection), and platelets (help blood clot). An automated test ensures accuracy. The differential count provides detailed information about white cell types.
348 services278 patients
Blood test, comprehensive group of blood chemicals 80053
A comprehensive group of blood chemicals test, also known as a comprehensive metabolic panel, is a blood test that measures your sugar level, electrolyte and fluid balance, kidney function, and liver function. This helps to check your body's overall health.
A TSH blood test measures the level of thyroid stimulating hormone in your body. This hormone is produced by the pituitary gland and regulates how your thyroid works. It's a simple procedure where a small amount of blood is drawn from your arm for analysis.
164 services146 patients
Blood test, basic group of blood chemicals (calcium, total) 80048
A basic group blood test measures the levels of certain chemicals in your blood, including calcium. This helps assess your overall health and detect potential problems. The procedure involves drawing a small amount of blood from your arm, which is then analyzed in a lab.
162 services126 patients
Blood test, lipids (cholesterol and triglycerides) 80061
A lipid panel is a blood test that measures fats and fatty substances, such as cholesterol and triglycerides. These substances are used by your body as a source of energy. High levels can lead to health issues, including heart disease.
147 services139 patients
Gene analysis (mutl homolog 1, colon cancer, nonpolyposis type 2) full sequence analysis 81292
Gene analysis, specifically for MUTL Homolog 1, linked to colon cancer, involves studying your DNA sequence. This helps identify any changes or mutations that might increase your risk of developing colon cancer. It's a preventive measure to manage potential health risks.
141 services141 patients
Blood test, clotting time 85610
A clotting time blood test helps determine how quickly your blood forms clots, a process crucial to stop bleeding. During the test, a small blood sample is taken from your arm. The sample is then analyzed in a lab to see how long it takes for a clot to form.
130 services26 patients
Gene analysis (phosphatase and tensin homolog), full sequence analysis 81321
Gene analysis, specifically phosphatase and tensin homolog (PTEN) full sequence analysis, is a test that looks at your DNA to identify any changes in the PTEN gene. This gene helps control cell growth and division. Changes may lead to certain health conditions.
97 services97 patients
Urinalysis, manual test 81002
A urinalysis is a simple, non-invasive test that checks the urine for various elements such as sugar, protein, and signs of infection. It can help detect many common conditions, including kidney disease and diabetes. The manual test involves a lab technician examining a urine sample.
96 services81 patients
Thyroxine (thyroid chemical), free 84439
The Thyroxine (thyroid chemical), free test is a blood test that measures the level of free T4 in your body. T4 is a hormone produced by your thyroid gland and is essential for growth and metabolism. If your T4 levels are too high or too low, it could indicate a thyroid disorder.
66 services58 patients
Hemoglobin a1c level 83036
Hemoglobin A1c (HbA1c) is a test that measures your average blood sugar level over the past 2-3 months. It's used to monitor how well diabetes is being controlled. High levels may indicate that your diabetes treatment plan needs adjustment.
65 services62 patients
Complete blood cell count (red cells, white blood cell, platelets), automated test 85027
A complete blood cell count (CBC) is an automated test that measures different components of the blood, including red cells, white cells, and platelets. It helps assess overall health, detect disorders like anemia or infection, and monitor medical treatments.
62 services59 patients
Magnesium level 83735
A magnesium level test is a simple blood test that measures the amount of magnesium in your body. Magnesium is a crucial mineral that helps your nerves, muscles, and heart function properly. The test can help detect health conditions like kidney disease or malnutrition.
51 services44 patients
Vitamin d-3 level 82306
A Vitamin D-3 level test measures the amount of Vitamin D-3, a crucial nutrient, in your body. This test helps identify if your levels are too low or too high. Low levels may lead to bone weakness, while high levels could harm your kidneys. It's a simple blood test.
47 services42 patients
Cyanocobalamin (vitamin b-12) level 82607
A Cyanocobalamin (Vitamin B-12) level test is a blood test that checks the amount of Vitamin B-12 in your body. This vitamin is vital for nerve function and the creation of red blood cells. Low or high levels could indicate a potential health issue.
24 services24 patients
Manual urinalysis test with examination using microscope, automated 81001
A manual urinalysis test with automated microscopic examination is a lab process that checks your urine for health indicators. It involves a machine scanning your sample to identify any abnormal elements, which can assist in diagnosing various conditions.
23 services22 patients
Iron level 83540
An iron level test measures the amount of iron in your blood. Iron is crucial for producing hemoglobin, a protein in red blood cells that carries oxygen throughout your body. This test helps identify iron deficiencies or excesses, which can lead to conditions like anemia or hemochromatosis.
18 services18 patients
Thyroxine (thyroid chemical), total 84436
A Thyroxine (thyroid chemical) total test measures the amount of thyroxine, a hormone produced by your thyroid gland, in your blood. This hormone helps regulate your body's metabolism. The test can help diagnose thyroid disorders, such as hypothyroidism or hyperthyroidism.
16 services16 patients
Gene analysis (breast cancer 2) of full sequence 81216
Gene analysis (breast cancer 2) of full sequence is a test that studies your DNA to identify any changes or mutations in the genes associated with an increased risk of certain types of cancer.
14 services14 patients
Phosphate level 84100
A phosphate level test measures the amount of phosphate in your blood. Phosphate is a chemical that contains the mineral phosphorus, crucial for energy production, muscle and nerve function, and bone growth. Imbalances may indicate kidney disease or other health issues.
11 services11 patients
Other Providers at the Same Location NPPES
Providers registered at the same practice address, or within the immediate area, according to the NPPES registry.
Common questions about this NPI record, answered from the official NPPES registry and CMS datasets shown on this page.
What is Star Laboratory's NPI number?
The NPI number for Star Laboratory is 1134439573. It was assigned to this organization in the NPPES registry on October 19, 2010.
Where is Star Laboratory located?
Star Laboratory is located at 125 Fleming St, Piscataway, NJ 08854. The listed phone number is (732) 529-5100.
What is Star Laboratory's specialty?
The primary specialty registered for this NPI is Clinical Medical Laboratory with taxonomy code 291U00000X.
Does Star Laboratory hold a CLIA laboratory certificate?
Yes. A Certificate of Accreditation (number 31D2014717) is associated with this NPI, valid through October 1, 2027. CLIA certificates authorize laboratory testing under the federal Clinical Laboratory Improvement Amendments program.
When was this NPI record last updated?
The NPPES record for Star Laboratory was last updated on October 9, 2019. NPI Profile syncs weekly with the NPPES registry data releases published by CMS. This NPI record was last updated 6 years ago. If this record has changed at CMS more recently, you can request an on-demand re-check against the live CMS registry, directly from this page.
# Star Laboratory · NPI 1134439573
Clinical Medical Laboratory organization in Piscataway, New Jersey. Organization record, active in the CMS NPPES registry since October 19, 2010.
## Identity
- **NPI:** 1134439573 (Entity type: Organization)
- **Enumerated:** October 19, 2010
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Organization subpart:** No
- **Authorized official:** Sam Khawaja, CEO
## Practice location
- **Address:** 125 FLEMING ST, Piscataway, NJ 08854-3350
- **Phone:** (732) 529-5100 · **Fax:** (732) 474-0923
## Record status
- **NPPES last updated:** October 9, 2019
- **Other identifiers:** Other 0004918 (NJ)
- **CLIA laboratory certificates:** 1 on file
---
Source: [NPI Profile](https://npiprofile.com/npi/1134439573) · Data from the CMS NPPES public registry.
# Star Laboratory · NPI 1134439573
Clinical Medical Laboratory organization in Piscataway, New Jersey. Organization record, active in the CMS NPPES registry since October 19, 2010.
## Identity
- **NPI:** 1134439573 (Entity type: Organization)
- **Enumerated:** October 19, 2010
- **Primary specialty:** Clinical Medical Laboratory · taxonomy 291U00000X
- **Organization subpart:** No
- **Authorized official:** Sam Khawaja, CEO
## Practice location
- **Address:** 125 FLEMING ST, Piscataway, NJ 08854-3350
- **Phone:** (732) 529-5100 · **Fax:** (732) 474-0923
## Record status
- **NPPES last updated:** October 9, 2019
- **Other identifiers:** Other 0004918 (NJ)
- **CLIA laboratory certificates:** 1 on file
---
Source: [NPI Profile](https://npiprofile.com/npi/1134439573) · Data from the CMS NPPES public registry.