| Gene | GDB AccessionID | Location | OMIM Link |
|---|
| ADA |
GDB:119649 | 20q12-20q13.11 20q13.11-20q13.11 |
ADENOSINE DEAMINASE; ADA
|
| AGS |
GDB:119662 | 20p12-20p12 |
CHOLESTASIS WITH PERIPHERAL PULMONARY STENOSIS
|
| AHCY |
GDB:118983 | 20cen-20q13.1 |
S-ADENOSYLHOMOCYSTEINE HYDROLASE; AHCY
|
| AVP |
GDB:119009 | 20p13-20p13 |
DIABETES INSIPIDUS, NEUROHYPOPHYSEAL TYPE
ARGININE VASOPRESSIN; AVP
|
| CDAN2 |
GDB:9823270 | 20q11.2-20q11.2 |
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE II
|
| CDMP1 |
GDB:438940 | 20q11.2-20q11.2 |
CHONDRODYSPLASIA, GREBE TYPE
CARTILAGE-DERIVED MORPHOGENETIC PROTEIN 1
|
| CHRNA4 |
GDB:128169 | 20q13.2-20q13.3 |
CHOLINERGIC RECEPTOR, NEURONAL NICOTINIC, ALPHA POLYPEPTIDE 4; CHRNA4
|
| CST3 |
GDB:119817 | 20p11.2-20p11.2 |
AMYLOIDOSIS VI
|
| EBN1 |
GDB:119855 | 20q13.2-20q13.3 |
EPILEPSY, BENIGN NEONATAL; EBN1
POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 2
|
| EDN3 |
GDB:119862 | 20q13.2-20q13.3 |
ENDOTHELIN-3; EDN3
WAARDENBURG-SHAH SYNDROME
|
| EEGV1 |
GDB:127525 | 20q13.2-20q13.3 |
ELECTROENCEPHALOGRAM, LOW-VOLTAGE
|
| FTLL1 |
GDB:119235 | 20q12-20qter |
FERRITIN LIGHT CHAIN; FTL
|
| GNAS1 |
GDB:120628 | 20q13.2-20q13.3 20q13.2-20q13.2 |
GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-STIMULATING POLYPEPTIDE;
|
| HNF4A |
GDB:393281 | 20q12-20q13.1 |
TRANSCRIPTION FACTOR 14, HEPATIC NUCLEAR FACTOR; TCF14
|
| JAG1 |
GDB:6175920 | 20p12-20p12 20p12.2-20p12.2 |
JAGGED 1; JAG1
|
| KCNQ2 |
GDB:9787229 | 20q13.3-20q13.3 |
POTASSIUM CHANNEL, VOLTAGE-GATED, SUBFAMILY Q, MEMBER 2
|
| MKKS |
GDB:9860197 | 20p12-20p12 |
HYDROMETROCOLPOS SYNDROME
|
| MODY1 |
GDB:128145 | 20q12-20q13.1 |
DIABETES MELLITUS, AUTOSOMAL DOMINANT
|
| NBIA1 |
GDB:4252819 | 20p13-20p12.3 |
HALLERVORDEN-SPATZ DISEASE
|
| PCK1 |
GDB:125349 | 20q13.2-20q13.31 20q13.31-20q13.31 |
PHOSPHOENOLPYRUVATE CARBOXYKINASE 1, SOLUBLE; PCK1
|
| PI3 |
GDB:203940 | 20q12-20q13 |
PROTEINASE INHIBITOR 3; PI3
|
| PPGB |
GDB:119507 | 20q13.1-20q13.1 |
NEURAMINIDASE DEFICIENCY WITH BETA-GALACTOSIDASE DEFICIENCY
|
| PPMD |
GDB:702144 | 20q11-20q11 |
CORNEAL DYSTROPHY, HEREDITARY POLYMORPHOUS POSTERIOR; PPCD
|
| PRNP |
GDB:120720 | 20pter-20p12 |
GERSTMANN-STRAUSSLER DISEASE; GSD
PRION PROTEIN; PRNP
|
| THBD |
GDB:119613 | 20p11.2-20p11.2 |
THROMBOMODULIN; THBD
|
| TOP1 |
GDB:120444 | 20q11.2-20q13.1 20q12-20q13.1 |
TOPOISOMERASE (DNA) I; TOP1
|