ScopeUniversitätsklinikum Tübingen Institut für Medizinische Genetik und Angewandte Genomik
37 capabilities
Accredited since July 2024
Verified Apr 2026
One of 3,039 in Germany
Details
Calwerstraße 7
Tübingen 72076 , Germany
Tübingen 72076 , Germany
Accreditation
Active
DAkkS
D-ML-13130-04-00
Provides molecular genetic testing for hereditary disorders including ataxias and tumor predisposition syndromes using PCR, DNA sequencing, and fragment length analysis on blood and tissue samples.
Accreditation Details
Accreditation Body
DAkkS
Number
D-ML-13130-04-00
Status
ActiveSince
08 July 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 (37)
| Standard Reference | Description | Category |
|---|---|---|
| (HFE) | Hämochromatose (HFE) | Elemental Analysis |
| (PMP22) | Neuropathie Typ 1 (PMP22) | Elemental Analysis |
| (RB1) | Retinoblastom (RB1) | Elemental Analysis |
| (Somatik) | (Somatik) | Elemental Analysis |
| (UGT1A1) | Morbus Meulengracht (UGT1A1) | Elemental Analysis |
| (kleine Varianten und CNV) | (kleine Varianten und CNV) | Elemental Analysis |
| ARVC (DSC2, DSG2, DSP, JUP, PKP2, TMEM43) | ARVC (DSC2, DSG2, DSP, JUP, PKP2, TMEM43) | Elemental Analysis |
| Ataxien (FXN, SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA10, SCA12, SCA17, ATN1, AR) | Ataxien (FXN, SCA1, SCA2, SCA3, SCA6, SCA7, SCA8, SCA10, SCA12, SCA17, ATN1, AR) | Elemental Analysis |
| C9ORF72 | C9orf72 | Elemental Analysis |
| Chorea Huntington (HTT) | Chorea Huntington (HTT) | Elemental Analysis |
| Chorea-artige Erkrankungen (PRNP, JPH3) | Chorea-artige Erkrankungen (PRNP, JPH3) | Elemental Analysis |
| Cystische Fibrose (CFTR) | Cystische Fibrose (CFTR) | Elemental Analysis |
| DCM (LMNA, MYBPC3, MYH7, TNNT2) | DCM (LMNA, MYBPC3, MYH7, TNNT2) | Elemental Analysis |
| Deletionen | Insertionen/Deletionen | Elemental Analysis |
| HCM (MYBPC3, MYH7, TNNT2, TNNI3, TPM1) | HCM (MYBPC3, MYH7, TNNT2, TNNI3, TPM1) | Elemental Analysis |
| Hereditäre Motorisch-Sensible | Hereditäre motorisch-sensible | Elemental Analysis |
| Inaktivierung (AR) | X-Inaktivierung (AR) | Elemental Analysis |
| Kardiomyopathien | Kardiomyopathien | Elemental Analysis |
| LVNC (MYH7, MYBPC3, TNNT2, LDB3) | LVNC (MYH7, MYBPC3, TNNT2, LDB3) | Elemental Analysis |
| Morbus Gaucher (GBA) | Morbus Gaucher (GBA) | Elemental Analysis |
| Morbus Krabbe (GALC) | Morbus Krabbe (GALC) | Elemental Analysis |
| PRSS1) | Pankreatitis (PRSS1) | Elemental Analysis |
| Pankreatitis (SPINK1) | Pankreatitis (SPINK1) | Elemental Analysis |
| RCM (TNNI3, TNNT2) | RCM (TNNI3, TNNT2) | Elemental Analysis |
| Tumor-Prädispositionen: Brust- | Tumor-Prädispositionen: Brust- | Elemental Analysis |
| Whole Exome Sequenzierung (WES) | Whole Exome Sequenzierung (WES) | Elemental Analysis |
| Whole Genome Sequenzierung | Whole Genome Sequenzierung | Elemental Analysis |
| (STK11) | Peutz-Jeghers-Syndrom (STK11) | Molecular Diagnostics / PCR |
| (TP53) | Li-Fraumeni-Syndrom (TP53) | Molecular Diagnostics / PCR |
| Cowden-Syndrom (PTEN) | Cowden-Syndrom (PTEN) | Molecular Diagnostics / PCR |
| Hereditäres Magenkarzinom (CDH1) | Hereditäres Magenkarzinom (CDH1) | Molecular Diagnostics / PCR |
| Metachromatische Leukodystrophie | Metachromatische Leukodystrophie | Molecular Diagnostics / PCR |
| Sequenzierung: ABCG5, ABCG8, APOB, APOE, CYP27A1, DHCR7, DHCR24, LDLR, LDLRAP1, LIPA, NPC1L1, PCSK9, SORT1; CNV: | Whole-Exome-Sequenzierung | Molecular Diagnostics / PCR |
| (ARSA) | (ARSA) | Other |
| (WGS) | (WGS) | Other |
| FMR1 | Tremor-Ataxie-Syndrom (FMR1 | Other |
| NPC2) | NPC2) | Other |