| Gene | GDB AccessionID | Location | OMIM Link |
|---|
| ACCPN |
GDB:5457725 | 15q13-15q15 |
CORPUS CALLOSUM, AGENESIS OF, WITH NEURONOPATHY
|
| AHO2 |
GDB:9954535 | 15q11-15q13 |
HEREDITARY OSTEODYSTROPHY-2; AHO2
|
| ANCR |
GDB:119678 | 15q11-15q12 |
ANGELMAN SYNDROME
|
| B2M |
GDB:119028 | 15q21-15q22.2 |
BETA-2-MICROGLOBULIN; B2M
|
| BBS4 |
GDB:511199 | 15q22.3-15q23 |
BARDET-BIEDL SYNDROME, TYPE 4; BBS4
|
| BLM |
GDB:135698 | 15q26.1-15q26.1 |
BLOOM SYNDROME; BLM
|
| CAPN3 |
GDB:119751 | 15q15-15q15 15pter-15qter 15q15.1-15q21.1 |
CALPAIN, LARGE POLYPEPTIDE L3; CAPN3
MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2; LGMD2
|
| CDAN1 |
GDB:9823267 | 15q15.1-15q15.3 |
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE I
|
| CDAN3 |
GDB:386192 | 15q21-15q25 |
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE III; CDAN3
|
| CLN6 |
GDB:4073043 | 15q21-15q21 15q21-15q23 |
CEROID-LIPOFUSCINOSIS, NEURONAL 6, LATE INFANTILE, VARIANT; CLN6
|
| CMH3 |
GDB:138299 | 15q2-15q2 |
CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 3; CMH3
|
| CYP19 |
GDB:119830 | 15q21-15q21 15q21.1-15q21.1 |
CYTOCHROME P450, SUBFAMILY XIX; CYP19
|
| CYP1A1 |
GDB:120604 | 15q22-15q24 |
CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 1; CYP1A1
|
| CYP1A2 |
GDB:118780 | 15pter-15qter 15q22-15qter |
CYTOCHROME P450, SUBFAMILY I, POLYPEPTIDE 2; CYP1A2
|
| DYX1 |
GDB:1391796 | 15q21-15q21 |
DYSLEXIA, SPECIFIC, 1; DYX1
|
| EPB42 |
GDB:127385 | 15q15-15q15 |
PROTEIN 4.2, ERYTHROCYTIC; EPB42
|
| ETFA |
GDB:119121 | 15q23-15q25 |
GLUTARICACIDURIA IIA; GA IIA
|
| EYCL3 |
GDB:4590306 | 15q11-15q21 |
EYE COLOR-3; EYCL3
|
| FAH |
GDB:119901 | 15q23-15q25 |
TYROSINEMIA, TYPE I
|
| FBN1 |
GDB:127115 | 15q21.1-15q21.1 |
FIBRILLIN-1; FBN1
MARFAN SYNDROME; MFS
|
| FES |
GDB:119906 | 15q26.1-15q26.1 |
V-FES FELINE SARCOMA VIRAL/V-FPS FUJINAMI AVIAN SARCOMA VIRAL ONCOGENE
|
| HCVS |
GDB:119306 | 15q11-15qter |
CORONAVIRUS 229E SUSCEPTIBILITY; CVS
|
| HEXA |
GDB:120040 | 15q23-15q24 |
TAY-SACHS DISEASE; TSD
|
| IVD |
GDB:119354 | 15q14-15q15 |
ISOVALERICACIDEMIA; IVA
|
| LIPC |
GDB:119366 | 15q21-15q22 15q21-15q23 |
LIPASE, HEPATIC; LIPC
|
| MYO5A |
GDB:218824 | 15q21-15q21 |
MYOSIN VA; MYO5A
|
| OCA2 |
GDB:136820 | 15q11.2-15q12 |
ALBINISM II
|
| OTSC1 |
GDB:9860473 | 15q25-15q26 |
OTOSCLEROSIS
|
| PWCR |
GDB:120325 | 15q11-15q12 |
PRADER-WILLI SYNDROME
|
| RLBP1 |
GDB:127341 | 15q26-15q26 |
RETINALDEHYDE-BINDING PROTEIN 1,; RLBP1
|
| SLC12A1 |
GDB:386121 | 15q15-15q21 |
SOLUTE CARRIER FAMILY 12, MEMBER 1; SLC12A1
|
| SPG6 |
GDB:511201 | 15q11.2-15q12 |
SPASTIC PARAPLEGIA 6, AUTOSOMAL DOMINANT; SPG6
|
| TPM1 |
GDB:127875 | 15q22-15q22 15q22.1-15q22.1 |
TROPOMYOSIN 1; TPM1
|
| UBE3A |
GDB:228487 | 15q11-15q13 |
ANGELMAN SYNDROME
UBIQUITIN-PROTEIN LIGASE E3A; UBE3A
|
| WMS |
GDB:5583902 | 15q21.1-15q21.1 |
WEILL-MARCHESANI SYNDROME
|