| Gene | GDB AccessionID | Location | OMIM Link |
|---|
| CACNB2 |
GDB:132014 | 10p12-10p12 |
CALCIUM CHANNEL, VOLTAGE-DEPENDENT, BETA-2 SUBUNIT; CACNB2
|
| COL17A1 |
GDB:131396 | 10q24.3-10q24.3 |
COLLAGEN, TYPE XVII, ALPHA-1 POLYPEPTIDE; COL17A1
|
| CUBN |
GDB:636049 | 10p12.1-10p12.1 |
MEGALOBLASTIC ANEMIA 1; MGA1
|
| CYP17 |
GDB:119829 | 10q24.3-10q24.3 |
ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 17-ALPHA-HYDROXYLASE DEFICIENCY
|
| CYP2C19 |
GDB:131456 | 10q24-10q24 |
CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19
|
| CYP2C9 |
GDB:131455 | 10q24.1-10q24.1 |
CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 9; CYP2C9
|
| CYP2C |
GDB:119831 | 10q24.1-10q24.3 |
CYTOCHROME P450, SUBFAMILY IIC, POLYPEPTIDE 19; CYP2C19
|
| EGR2 |
GDB:120611 | 10q21.1-10q21.1 |
EARLY GROWTH RESPONSE-2; EGR2
|
| EMX2 |
GDB:277886 | 10q26.1-10q26.1 |
EMPTY SPIRACLES, DROSOPHILA, 2, HOMOLOG OF; EMX2
|
| EPT |
GDB:9786112 | 10q23.3-10q24.1 |
EPILEPSY, PARTIAL; EPT
|
| ERCC6 |
GDB:119882 | 10q11-10q21 10q11-10q11 10q21.1-10q21.1 |
EXCISION-REPAIR CROSS-COMPLEMENTING RODENT REPAIR DEFICIENCY, COMPLEMENTATION
|
| FGFR2 |
GDB:127273 | 10q25.3-10q26 10q26-10q26 |
FIBROBLAST GROWTH FACTOR RECEPTOR-2; FGFR2
|
| HK1 |
GDB:120044 | 10q22-10q22 |
HEXOKINASE-1; HK1
|
| HOX11 |
GDB:119607 | 10q24-10q24 |
HOMEO BOX-11; HOX11
|
| HPS |
GDB:127359 | 10q23.1-10q23.3 |
HERMANSKY-PUDLAK SYNDROME; HPS
|
| IL2RA |
GDB:119345 | 10p15-10p14 |
INTERLEUKIN-2 RECEPTOR, ALPHA; IL2RA
|
| LIPA |
GDB:120153 | 10q24-10q25 10q23.2-10q23.3 |
WOLMAN DISEASE
|
| MAT1A |
GDB:129077 | 10q-10q 10q22-10q22 |
METHIONINE ADENOSYLTRANSFERASE DEFICIENCY
|
| MBL2 |
GDB:120167 | 10q11.2-10q11.2 |
MANNOSE-BINDING PROTEIN, SERUM; MBP1
|
| MHAM |
GDB:118839 | 10q22-10q23 |
MULTIPLE HAMARTOMA SYNDROME; MHAM
|
| MKI67 |
GDB:120185 | 10q25-10qter |
PROLIFERATION-RELATED Ki-67 ANTIGEN; MKI67
|
| MXI1 |
GDB:137182 | 10q25-10q25 10q24-10q25 |
MAX INTERACTING PROTEIN 1; MXI1
|
| OAT |
GDB:120246 | 10q26-10q26 |
ORNITHINE AMINOTRANSFERASE DEFICIENCY
|
| OATL3 |
GDB:215803 | 10q26-10q26 |
ORNITHINE AMINOTRANSFERASE DEFICIENCY
|
| PAX2 |
GDB:138771 | 10q24-10q24 10q25-10q25 |
PAIRED BOX HOMEOTIC GENE 2; PAX2
|
| PCBD |
GDB:138478 | 10q22-10q22 |
PTERIN-4-ALPHA-CARBINOLAMINE DEHYDRATASE; PCBD
PRIMAPTERINURIA
|
| PEO1 |
GDB:632784 | 10q23.3-10q24.3 |
PROGRESSIVE EXTERNAL OPHTHALMOPLEGIA; PEO
|
| PHYH |
GDB:9263423 | 10p15.3-10p12.2 |
REFSUM DISEASE
PHYTANOYL-CoA HYDROXYLASE; PHYH
|
| PNLIP |
GDB:127916 | 10q24-10q26 10q26.1-10q26.1 |
LIPASE, CONGENITAL ABSENCE OF PANCREATIC
|
| PSAP |
GDB:120366 | 10q21-10q22 10q22.1-10q22.1 |
PROSAPOSIN; PSAP
|
| PTEN |
GDB:6022948 | 10q23-10q23 10q23.3-10q23.3 |
POLYPOSIS, JUVENILE INTESTINAL
PHOSPHATASE AND TENSIN HOMOLOG; PTEN
|
| RBP4 |
GDB:120342 | 10q23-10q24 |
RETINOL-BINDING PROTEIN, PLASMA; RBP4
|
| RDPA |
GDB:9954445 | 10pter-10p11.2 |
REFSUM DISEASE WITH INCREASED PIPECOLICACIDEMIA; RDPA
|
| RET |
GDB:120346 | 10q11.2-10q11.2 |
RET PROTO-ONCOGENE; RET
|
| SDF1 |
GDB:433267 | 10q11.2-10q11.2 10q11.1-10q11.1 |
STROMAL CELL-DERIVED FACTOR 1; SDF1
|
| SFTPA1 |
GDB:119593 | 10q22-10q23 |
PULMONARY SURFACTANT APOPROTEIN PSP-A; PSAP
|
| SFTPD |
GDB:132674 | 10q22.2-10q23.1 |
PULMONARY SURFACTANT APOPROTEIN PSP-D; PSP-D
|
| SHFM3 |
GDB:386030 | 10q24-10q25 |
SPLIT-HAND/FOOT MALFORMATION, TYPE 3; SHFM3
|
| SIAL |
GDB:6549924 | 10pter-10q23 |
NEURAMINIDASE DEFICIENCY
|
| TNFRSF6 |
GDB:132671 | 10q24.1-10q24.1 |
APOPTOSIS ANTIGEN 1; APT1
|
| UFS |
GDB:6380714 | 10q23-10q24 |
UROFACIAL SYNDROME; UFS
|
| UROS |
GDB:128112 | 10q25.2-10q26.3 |
PORPHYRIA, CONGENITAL ERYTHROPOIETIC; CEP
|