- Analytes
- TG
TG
Name: |
thyroglobulin
|
Symbol: |
TG
|
Version of Orphanet: |
2022-05-01 04:55:23
|
Synonyms: |
AITD3
TGN
|
XREF(s): | |
Created: |
13 May 2019 - 01:01
|
Changed: |
01 May 2022 - 06:55
|
-
Endocrine Disorders - Hypothyroidism (42 genes) - ULB
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments DUOX2 100.00 0 Endocrine Disorders - Hypothyroidism DUOXA2 100.00 0 Endocrine Disorders - Hypothyroidism FOXE1 85.24 0 Endocrine Disorders - Hypothyroidism GAS1 78.95 0 Endocrine Disorders - Hypothyroidism GLIS3 100.00 0 Endocrine Disorders - Hypothyroidism GNA11 99.57 0 Endocrine Disorders - Hypothyroidism GNAS 100.00 0 Endocrine Disorders - Hypothyroidism GNAS-AS1 100.00 0 Endocrine Disorders - Hypothyroidism HESX1 100.00 0 Endocrine Disorders - Hypothyroidism IGSF1 100.00 0 Endocrine Disorders - Hypothyroidism IYD 100.00 0 Endocrine Disorders - Hypothyroidism LHX3 90.58 0 Endocrine Disorders - Hypothyroidism LHX4 100.00 0 Endocrine Disorders - Hypothyroidism NKX2-1 97.73 0 Endocrine Disorders - Hypothyroidism NKX2-5 100.00 0 Endocrine Disorders - Hypothyroidism OTX2 100.00 0 Endocrine Disorders - Hypothyroidism PAX8 99.96 0 Endocrine Disorders - Hypothyroidism POU1F1 100.00 0 Endocrine Disorders - Hypothyroidism PRKAR1A 100.00 0 Endocrine Disorders - Hypothyroidism PROP1 100.00 0 Endocrine Disorders - Hypothyroidism SECISBP2 97.69 0 Endocrine Disorders - Hypothyroidism SLC5A5 99.97 0 Endocrine Disorders - Hypothyroidism SLC16A2 99.51 0 Endocrine Disorders - Hypothyroidism SLC26A4 99.97 0 Endocrine Disorders - Hypothyroidism SOX3 97.06 0 Endocrine Disorders - Hypothyroidism STX16 99.93 0 Endocrine Disorders - Hypothyroidism TBL1X 99.87 0 Endocrine Disorders - Hypothyroidism TG 100.00 0 Endocrine Disorders - Hypothyroidism THRA 100.00 0 Endocrine Disorders - Hypothyroidism THRB 100.00 0 Endocrine Disorders - Hypothyroidism THPO 99.80 0 Endocrine Disorders - Hypothyroidism TRHR 100.00 0 Endocrine Disorders - Hypothyroidism TSHB 100.00 0 Endocrine Disorders - Hypothyroidism TSHR 100.00 0 Endocrine Disorders - Hypothyroidism -
Thyroid disgenesis (38 genes) - VUB
Gene % of coding sequence sufficiently covered to detect heterozygous mutations Copy number variation Comments AP2S1 100.00 0 No comment CASR 100.00 0 No comment CDCA8 100.00 0 No comment DUOX1 100.00 0 No comment DUOX2 100.00 0 No comment DUOXA2 100.00 0 No comment DYRK1A 100.00 0 No comment ELN 100.00 0 No comment FOXE1 60.48 0 No comment GAS1 62.99 0 No comment GLIS3 100.00 0 No comment GNA11 99.51 0 No comment GNAS 98.96 0 No comment GNAS-AS1 100.00 0 No comment IYD 100.00 0 No comment JAG1 99.66 0 No comment KAT6B 100.00 0 No comment KDM6A 100.00 0 No comment KMT2D 100.00 0 No comment NKX2-1 92.46 0 No comment NKX2-5 100.00 0 No comment NTN1 95.84 0 No comment PAX8 100.00 0 No comment SALL1 100.00 0 No comment SECISBP2 98.68 0 No comment SLC11A2 100.00 0 No comment SLC26A4 99.99 0 No comment SLC26A7 100.00 0 No comment SLC5A5 100.00 0 No comment STX16 100.00 0 No comment TBX1 77.39 0 No comment TG 100.00 0 No comment THRA 100.00 0 No comment THRB 100.00 0 No comment THPO 99.84 0 No comment TSHR 100.00 0 No comment TUBB1 100.00 0 No comment URB1 99.99 0 No comment