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Gene

BUB1B-BUB1 mitotic checkpoint serine/threonine kinase B
Also know as: BUB1beta, BUBR1, Bub1A, MAD3L, MVA1, SSK1, hBUBR1; GeneID:701; Location:15q15.1;
Associated conditions: Colorectal cancer;  Mosaic variegated aneuploidy syndrome 1;  Premature chromatid separation trait
Results:
76 genetic tests from 27 labs with tests matching your search, 2 labs matching in other ways
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Tests names and labsConditionsGenes, analytes, and microbesMethods

Tempus xT

Tempus AI - RTP
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Hereditary Cancer Screening - Colorectal & Gastric Cancer Panel (including Pancreatic Cancer) - (43 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
5843
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Renal/Urinary Tract Cancer Panel (Including prostate and kidney cancer) - (39 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
4039
  • X Mutation scanning of select exons

Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes)

Genesys Diagnostics, Genesys Diagnostics, Inc.
United States
10999
  • X Mutation scanning of select exons

Hereditary Wilms Tumor Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
19
  • C Sequence analysis of the entire coding region

Hereditary Expanded Cancer Panel

Mayo Clinic Laboratories, Mayo Clinic
United States
186
  • C Sequence analysis of the entire coding region

Tempus xT

Tempus AI - CHI
United States
2647
  • I Microsatellite instability testing (MSI)
  • C Sequence analysis of the entire coding region

Multigene panel for epilepsies based on whole-exome sequencing

CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
Portugal
1646
  • S Mutation scanning of the entire coding region

MVL Vision Panel

Molecular Vision Laboratory
United States
16541199
  • D Deletion/duplication analysis
  • C Sequence analysis of the entire coding region

Endeavor

PathGroup
United States
73505
  • C Sequence analysis of the entire coding region

Colorectal cancer, somatic, 114500 (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

Mosaic variegated aneuploidy syndrome 1, 257300, Autosomal recessive; MVA1 (Mosaic variegated aneuploidy syndrome) (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

[Premature chromatid separation trait], 176430, Autosomal dominant (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal)

Intergen Genetics and Rare Diseases Diagnosis Center
Turkey
11
  • C Sequence analysis of the entire coding region

qGenEx Intellectual disability

Quantitative Genomic Medicine Laboratories, SL
Spain
31969
  • S Mutation scanning of the entire coding region
  • C Sequence analysis of the entire coding region

PrimBio Colorectal Cancer Panel

PrimBio Research Institute
United States
152
  • C Sequence analysis of the entire coding region

Ataxia/Episodic Ataxia Disorders (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1536
  • C Sequence analysis of the entire coding region

Comprehensive Neuropathies (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1869
  • C Sequence analysis of the entire coding region

Comprehensive Muscular Dystrophy/Myopathy (NGS Panel and Copy Number Analysis + mtDNA)

MNG Laboratories (Medical Neurogenetics, LLC.)
United States
1911
  • C Sequence analysis of the entire coding region

Intellectual Disability Panel and/or Autism

CGC Genetics, Unilabs
Portugal
11651
  • C Sequence analysis of the entire coding region

Hereditary Pan-cancer panel

CGC Genetics, Unilabs
Portugal
1205
  • C Sequence analysis of the entire coding region
76 tests from 27 labs
See all labs
View the list of labs matching your search query.
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❮Page 1 of 4❯
Tempus xT by Tempus AI - RTP
2 conditions, 647 genes
Hereditary Cancer Screening - Colorectal & Gastric Cancer Panel (including Pancreatic Cancer) - (43 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
58 conditions, 43 genes
Hereditary Cancer Screening - Renal/Urinary Tract Cancer Panel (Including prostate and kidney cancer) - (39 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
40 conditions, 39 genes
Hereditary Cancer Screening - Full Hereditary Cancer Panel (99 Genes) by Genesys Diagnostics, Genesys Diagnostics, Inc.
109 conditions, 99 genes
Hereditary Wilms Tumor Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 9 genes
Hereditary Expanded Cancer Panel by Mayo Clinic Laboratories, Mayo Clinic
1 condition, 86 genes
Tempus xT by Tempus AI - CHI
2 conditions, 647 genes
Multigene panel for epilepsies based on whole-exome sequencing by CGPP - Center for Predictive and Preventive Genetics, IBMC - Institute for Cell and Molecular Biology
1 condition, 646 genes
MVL Vision Panel by Molecular Vision Laboratory
1654 conditions, 1199 genes
Endeavor by PathGroup
73 conditions, 505 genes
Colorectal cancer, somatic, 114500 (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
Mosaic variegated aneuploidy syndrome 1, 257300, Autosomal recessive; MVA1 (Mosaic variegated aneuploidy syndrome) (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
[Premature chromatid separation trait], 176430, Autosomal dominant (BUB1B gene) (Sequence Analysis-All Coding Exons) (Postnatal) by Intergen Genetics and Rare Diseases Diagnosis Center
1 condition, 1 gene
qGenEx Intellectual disability by Quantitative Genomic Medicine Laboratories, SL
3 conditions, 1969 genes
PrimBio Colorectal Cancer Panel by PrimBio Research Institute
1 condition, 52 genes
Ataxia/Episodic Ataxia Disorders (NGS Panel and Copy Number Analysis + mtDNA) by MNG Laboratories (Medical Neurogenetics, LLC.)
1 condition, 536 genes
Comprehensive Neuropathies (NGS Panel and Copy Number Analysis + mtDNA) by MNG Laboratories (Medical Neurogenetics, LLC.)
1 condition, 869 genes
Comprehensive Muscular Dystrophy/Myopathy (NGS Panel and Copy Number Analysis + mtDNA) by MNG Laboratories (Medical Neurogenetics, LLC.)
1 condition, 911 genes
Intellectual Disability Panel and/or Autism by CGC Genetics, Unilabs
1 condition, 1651 genes
Hereditary Pan-cancer panel by CGC Genetics, Unilabs
1 condition, 205 genes

IMPORTANT NOTE: NIH does not independently verify information submitted to the GTR; it relies on submitters to provide information that is accurate and not misleading. NIH makes no endorsements of tests or laboratories listed in the GTR. GTR is not a substitute for medical advice. Patients and consumers with specific questions about a genetic test should contact a health care provider or a genetics professional.