ScopeUniversitätsklinikum Gießen und Marburg GmbH Zentrum für Humangenetik
47 capabilities
Accredited since August 2024
Verified Oct 2026
One of 3,209 in Germany
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Details
Baldingerstraße
Marburg 35033 , Germany
Marburg 35033 , Germany
Accreditation
Active
DAkkS
D-ML-13304-10-00
www.ukgm.de/ugm_2/deu/umr_hum/index.html
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Specialises in molecular human genetics testing, including next-generation sequencing and targeted gene analysis for genetic disorders using blood and tissue samples with amplification and sequencing-based techniques.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13304-10-00
Status
ActiveSince
02 August 2024
Accreditation is granted under EU Regulation 765/2008 and assessed against ISO/IEC 17025. Data sourced from official DAkkS records.
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Test Capabilities (47)
| Standard Reference | Description | Category |
|---|---|---|
| Whole Exome Sequenzierung (WES) | Whole Exome Sequenzierung (WES) | Elemental Analysis |
| (HBOC), Gene: BRCA1, BRCA2, | Mamma- und Ovarialkarzinom (HBOC), Gene: BRCA1, BRCA2, CHEK2, PALB2, RAD51C, ATM | Molecular Diagnostics / PCR |
| /4, Gene: CDC73, CDKN1B, MEN1 | /4, Gene: CDC73, CDKN1B, MEN1 | Molecular Diagnostics / PCR |
| 1, Gen: MEN1 | 1, Gen: MEN1 | Molecular Diagnostics / PCR |
| 2, Gene: RET | 2, Gene: RET | Molecular Diagnostics / PCR |
| Bannayan-Riley-Ruvalcaba- Syndrom, Gene: AKT1, PIK3CA, PTEN, SEC23B | Bannayan-Riley-Ruvalcaba- Syndrom, Gene: AKT1, PIK3CA, PTEN, SEC23B | Molecular Diagnostics / PCR |
| CDH1, CTNNA1 | CDH1, CTNNA1 | Molecular Diagnostics / PCR |
| Carney-Komplex, Gene: PRKAR1A, | Carney-Komplex, Gene: PRKAR1A, STK11 | Molecular Diagnostics / PCR |
| Cowden-Syndrom, Gene: AKT1, | Cowden-Syndrom, Gene: AKT1, PIK3CA, PTEN, SEC23B | Molecular Diagnostics / PCR |
| DiGeorge-Syndrom | DiGeorge-Syndrom | Molecular Diagnostics / PCR |
| Ehlers-Danlos-Syndrom, klassischer | Ehlers-Danlos-Syndrom, klassischer | Molecular Diagnostics / PCR |
| Ehlers-Danlos-Syndrom, vaskulärer | Ehlers-Danlos-Syndrom, vaskulärer | Molecular Diagnostics / PCR |
| Hereditäre Pankreatitis | Hereditäre Pankreatitis: SPINK1, PRSS1, CFTR-Gen | Molecular Diagnostics / PCR |
| Lynch-Syndrom, Gene: MLH1, MSH2, MSH6, PMS2, EPCAM | Lynch-Syndrom, Gene: MLH1, MSH2, MSH6, PMS2, EPCAM | Molecular Diagnostics / PCR |
| MET | MET | Molecular Diagnostics / PCR |
| MLH1, MSH2, MSH6, PMS2, EPCAM | MLH1, MSH2, MSH6, PMS2, EPCAM | Molecular Diagnostics / PCR |
| MLPA für STK11 | MLPA für STK11 | Molecular Diagnostics / PCR |
| MODY, Gene: ABCC8, APPL1, BLK, | MODY, Gene: ABCC8, APPL1, BLK, CEL, GCK, HNF1A, HNF1B, HNF4A, INS, KCNJ11, KLF11, NEUROD1, PAX4, PDX1, RFX6 | Molecular Diagnostics / PCR |
| Mamma- und Ovarialkarzinom | Mamma- und Ovarialkarzinom | Molecular Diagnostics / PCR |
| Mamma- und Ovarialkarzinom (HBOC), Gene: BRCA1, BRCA2, CHEK2, PALB2, RAD51C | Mamma- und Ovarialkarzinom (HBOC), Gene: BRCA1, BRCA2, CHEK2, PALB2, RAD51C | Molecular Diagnostics / PCR |
| Mamma- und Ovarialkarzinom, Gene: BRCA1, BRCA2 | Mamma- und Ovarialkarzinom, Gene: BRCA1, BRCA2 | Molecular Diagnostics / PCR |
| Marfan-Syndrom und Loeys-Dietz- Syndrom, Gene: FBN1, TGFBR1, TGFBR2 | Marfan-Syndrom und Loeys-Dietz- Syndrom, Gene: FBN1, TGFBR1, TGFBR2 | Molecular Diagnostics / PCR |
| Melanom: BAP1, CDK4, CDKN2A, | Melanom: BAP1, CDK4, CDKN2A, POT1, PTEN, TP53 | Molecular Diagnostics / PCR |
| Multiple Endokrine Neoplasie Typ | Multiple endokrine Neoplasie Typ | Molecular Diagnostics / PCR |
| Multiple Endokrine Neoplasie Typ 1 | Multiple Endokrine Neoplasie Typ 1 | Molecular Diagnostics / PCR |
| Neurofibromatose Typ 1 | Neurofibromatose Typ 1 | Molecular Diagnostics / PCR |
| Neurofibromatose Typ 1, Gen: NF1 | Neurofibromatose Typ 1, Gen: NF1 | Molecular Diagnostics / PCR |
| Neurofibromatose Typ 2 | Neurofibromatose Typ 2 | Molecular Diagnostics / PCR |
| Nierenzellkarzinom, hereditär, Gene: BAP1, FLCN, FH, MET, PTEN, SDHB, SDHD, TSC1, TSC2, VHL | Nierenzellkarzinom, hereditär, Gene: BAP1, FLCN, FH, MET, PTEN, SDHB, SDHD, TSC1, TSC2, VHL | Molecular Diagnostics / PCR |
| Noonan-Syndrom, Gene: PTPN11 | Noonan-Syndrom, Gene: PTPN11 | Molecular Diagnostics / PCR |
| Paragangliom-Phäochromozytom- Syndrom, Gene: AIP, MAX, MEN1, NF1, SDHA, SDHAF2, SDHB, SDHC, SDHD, RET, TMEM127, VHL | Paragangliom-Phäochromozytom- Syndrom, Gene: AIP, MAX, MEN1, NF1, SDHA, SDHAF2, SDHB, SDHC, SDHD, RET, TMEM127, VHL | Molecular Diagnostics / PCR |
| Prostatakarzinom | Prostatakarzinom: BRCA1, BRCA2, CHEK2, MSR1, RNASEL, HOXB13, PALB2, RAD51D | Molecular Diagnostics / PCR |
| Rhabdoid-Prädispositions-Syndrom, Gene: SMARCB1, SMARCA4 | Rhabdoid-Prädispositions-Syndrom, Gene: SMARCB1, SMARCA4 | Molecular Diagnostics / PCR |
| Schilddrüsenkarzinom, medulläres, Gen: RET | Schilddrüsenkarzinom, medulläres, Gen: RET | Molecular Diagnostics / PCR |
| Schilddrüsenkarzinom, papilläres, Gene: APC, CDKN1B, DICER1, PRKAR1A, PTEN | Schilddrüsenkarzinom, papilläres, Gene: APC, CDKN1B, DICER1, PRKAR1A, PTEN | Molecular Diagnostics / PCR |
| Thorakale Aortenerweiterung, Gene: ACTA2, COL3A1, FBN1, MYH11, MYLK, SMAD3, TGFB2, TGFBR1, TGFBR2 | Thorakale Aortenerweiterung, Gene: ACTA2, COL3A1, FBN1, MYH11, MYLK, SMAD3, TGFB2, TGFBR1, TGFBR2 | Molecular Diagnostics / PCR |
| Typ, Gen: COL3A1 | Typ, Gen: COL3A1 | Molecular Diagnostics / PCR |
| Typ, Gene: COL5A1, COL5A2, | Ehlers-Danlos-Syndrom, klassischer Typ, Gene: COL5A1, COL5A2, COL1A1 | Molecular Diagnostics / PCR |
| VHL | VHL | Molecular Diagnostics / PCR |
| Wilms-Tumor: WT1 | Wilms-Tumor: WT1 | Molecular Diagnostics / PCR |
| primärer Hyperparathyreoidismus, Gene: CASR, CDC73, CDKN1B, MEN1, RET | primärer Hyperparathyreoidismus, Gene: CASR, CDC73, CDKN1B, MEN1, RET | Molecular Diagnostics / PCR |
| Nierenzellkarzinom, papilläres, Gen: | Nierenzellkarzinom, papilläres, Gen: | Other |
| Pankreaskarzinom, Gene: ATM, | Pankreaskarzinom, Gene: ATM, | Other |
| Polyposis coli, Gene: APC, BMPR1A, | Polyposis coli, Gene: APC, BMPR1A, | Other |
| RASopathie, Gene: A2ML1, BRAF, | RASopathie, Gene: A2ML1, BRAF, | Other |
| Schwannomatose, Gene: LZTR1, | Schwannomatose, Gene: LZTR1, | Other |
| Tuberöse Sklerose, Gene: TSC1, | Tuberöse Sklerose, Gene: TSC1, | Other |
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