| Gene | GDB AccessionID | Location | OMIM Link |
|---|
| ATP7B |
GDB:120494 | 13q14.3-13q21.1 13q14.3-13q14.3 |
WILSON DISEASE; WND
|
| BRCA2 |
GDB:387848 | 13q12-13q13 13q12.3-13q12.3 |
BREAST CANCER 2, EARLY-ONSET; BRCA2
|
| BRCD1 |
GDB:9954522 | 13pter-13qter |
BREAST CANCER, DUCTAL, 1; BRCD1
|
| CLN5 |
GDB:230991 | 13q21.2-13q32 13q22-13q22 |
CEROID-LIPOFUSCNOSIS, NEURONAL 5; CLN5
|
| CPB2 |
GDB:129546 | 13pter-13qter 13q14.1-13q14.1 13q14.11-13q14.11 |
CARBOXYPEPTIDASE B2, PLASMA; CPB2
|
| ED2 |
GDB:9834522 | 13q11-13q12.1 |
ECTODERMAL DYSPLASIA, HIDROTIC; HED
|
| EDNRB |
GDB:129075 | 13q22-13q22 |
ENDOTHELIN-B RECEPTOR; EDNRB
|
| ENUR1 |
GDB:594516 | 13q13-13q14.3 |
ENURESIS, NOCTURNAL, 1; ENUR1
|
| ERCC5 |
GDB:120515 | 13q32-13q32 13q33-13q33 |
EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 5; ERCC5
|
| F10 |
GDB:119890 | 13q34-13q34 |
FACTOR X DEFICIENCY; F10
|
| F7 |
GDB:119897 | 13q34-13q34 |
FACTOR VII DEFICIENCY
|
| GJB2 |
GDB:125247 | 13q11-13q12.1 |
GAP JUNCTION PROTEIN, BETA-2, 26 KD; GJB2
DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 1; DFNB1
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 3; DFNA3
|
| HSCR2 |
GDB:128051 | 13q22-13q22 |
HIRSCHSPRUNG DISEASE-2; HSCR2
|
| IPF1 |
GDB:448899 | 13q12.1-13q12.1 |
INSULIN PROMOTER FACTOR 1; IPF1
|
| MBS1 |
GDB:128365 | 13q12.2-13q12.2 |
MOEBIUS SYNDROME; MBS
|
| MCOR |
GDB:9954520 | 13q31-13q32 |
CONGENITAL
|
| PCCA |
GDB:119473 | 13q32-13q32 |
GLYCINEMIA, KETOTIC, I
|
| RB1 |
GDB:118734 | 13q14.12-13q14.2 13q14.2-13q14.2 13q14.3-13q14.3 |
RETINOBLASTOMA; RB1
|
| RHOK |
GDB:371598 | 13q34-13q34 |
RHODOPSIN KINASE; RHOK
|
| SCZD7 |
GDB:9864734 | 13q32-13q32 |
DISORDER-2; SCZD2
|
| SGCG |
GDB:3763329 | 13q12-13q12 |
MUSCULAR DYSTROPHY, LIMB GIRDLE, TYPE 2C; LGMD2C
|
| SLC10A2 |
GDB:677534 | 13q33-13q33 |
SOLUTE CARRIER FAMILY 10, MEMBER 2; SLC10A2
|
| SLC25A15 |
GDB:120042 | 13q34-13q34 |
HYPERORNITHINEMIA-HYPERAMMONEMIA-HOMOCITRULLINURIA SYNDROME
|
| STARP1 |
GDB:635459 | 13pter-13qter |
STEROIDOGENIC ACUTE REGULATORY PROTEIN; STAR
|
| STGD2 |
GDB:642054 | 13q32-13q33 13q34-13q34 |
MACULAR DYSTROPHY WITH FLECKS, TYPE 2
|
| ZNF198 |
GDB:6382650 | 13q11-13q12 |
ZINC FINGER PROTEIN-198; ZNF198
|