Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB
Full name: |
Endocrine Disorders - Hyper(Hypo)parathyroidism (24 genes) - ULB
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Laboratory: | |
Created: |
10 Mar 2022 - 08:47
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Changed: |
12 Dec 2023 - 08:10
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Gene | % of coding sequence sufficiently covered to detect heterozygous mutations | Copy number variation | Comments |
---|---|---|---|
AIRE | 0.00 | 0 | , |
AP2S1 | 0.00 | 0 | , |
CASR | 0.00 | 0 | , |
CDC73 | 0.00 | 0 | , |
CDKN1A | 0.00 | 0 | , |
CDKN1B | 0.00 | 0 | , |
CDKN2B | 0.00 | 0 | , |
CDKN2C | 0.00 | 0 | , |
CHD7 | 0.00 | 0 | , |
FAM111A | 0.00 | 0 | , |
GATA3 | 0.00 | 0 | , |
GCM2 | 0.00 | 0 | , |
GNA11 | 0.00 | 0 | , |
MEN1 | 0.00 | 0 | , |
NEBL | 0.00 | 0 | , |
PTH | 0.00 | 0 | , |
PTH1R | 0.00 | 0 | , |
RET | 0.00 | 0 | , |
SEMA3E | 0.00 | 0 | , |
SOX3 | 0.00 | 0 | , |
STX16 | 0.00 | 0 | , |
TBCE | 0.00 | 0 | , |
TBX1 | 0.00 | 0 | , |
TRPV6 | 0.00 | 0 | , |