| Gene | GDB AccessionID | Location | OMIM Link |
|---|
| BCL2 |
GDB:119031 | 18q21.33-18q21.33 |
B-CELL CLL/LYMPHOMA 2; BCL2
|
| CNSN |
GDB:9954580 | 18q21.3-18q21.3 |
CARNOSINEMIA
|
| CORD1 |
GDB:118773 | 18q21.1-18q21.3 |
CONE-ROD DYSTROPHY-1; CORD1
|
| CYB5 |
GDB:125236 | 18q22.3-18q23 18q23-18q23 |
METHEMOGLOBINEMIA DUE TO DEFICIENCY OF CYTOCHROME b5
|
| DCC |
GDB:119838 | 18q21.1-18q21.1 18q21.3-18q21.3 |
DELETED IN COLORECTAL CARCINOMA; DCC
|
| F5F8D |
GDB:6919858 | 18q21-18q21 |
FACTOR V AND FACTOR VIII, COMBINED DEFICIENCY OF; F5F8D
|
| FECH |
GDB:127282 | 18q21.1-18q21.31 18q21.3-18q21.3 |
PROTOPORPHYRIA, ERYTHROPOIETIC
|
| FEO |
GDB:4378120 | 18q21.3-18q21.3 |
POLYOSTOTIC OSTEOLYTIC DYSPLASIA, HEREDITARY EXPANSILE; HEPOD
|
| FIC1 |
GDB:453352 | 18q-18q 18q21-18q22 18q21-18q21 |
CHOLESTASIS, PROGRESSIVE FAMILIAL INTRAHEPATIC 1; PFIC1
INTRAHEPATIC CHOLESTASIS
FAMILIAL INTRAHEPATIC CHOLESTASIS-1; FIC1
|
| HPE4 |
GDB:439246 | 18p11.3-18p11.3 |
HOLOPROSENCEPHALY, TYPE 4; HPE4
|
| LAMA3 |
GDB:251818 | 18q11.2-18q11.2 |
LAMININ, ALPHA 3; LAMA3
|
| LCFS2 |
GDB:9954578 | 18q11-18q12 |
CANCER
|
| MADH4 |
GDB:4642788 | 18q21.1-18q21.1 |
POLYPOSIS, JUVENILE INTESTINAL
MOTHERS AGAINST DECAPENTAPLEGIC, DROSOPHILA, HOMOLOG OF, 4; MADH4
|
| MAFD1 |
GDB:120163 | 18p-18p |
MANIC-DEPRESSIVE PSYCHOSIS, AUTOSOMAL
|
| MC2R |
GDB:135163 | 18p11.2-18p11.2 |
ADRENAL UNRESPONSIVENESS TO ACTH
|
| MCL |
GDB:9954574 | 18p11.32-18p11.32 |
LEIOMYOMATA, HEREDITARY MULTIPLE, OF SKIN
|
| MYP2 |
GDB:9862232 | 18p11.31-18p11.31 |
MYOPIA
|
| NPC1 |
GDB:138178 | 18q11-18q11 |
NIEMANN-PICK DISEASE, TYPE C1; NPC1
|
| SPPK |
GDB:606444 | 18q12-18q12 |
PALMOPLANTARIS STRIATA
|
| TGFBRE |
GDB:250852 | 18q22-18qter |
TRANSFORMING GROWTH FACTOR, BETA 1 RESPONSE ELEMENT
|
| TTR |
GDB:119471 | 18q12.1-18q12.1 |
TRANSTHYRETIN; TTR
|