Genes, Locations and Genetic Disorders on Chromosome 6

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ABCB2 GDB:1326686p21.3-6p21.3 TRANSPORTER 1, ABC; TAP1
ABCB3 GDB:1326696p21.3-6p21.3 TRANSPORTER 2, ABC; TAP2
ALDH5A1 GDB:4547676p22-6p22 SUCCINIC SEMIALDEHYDE DEHYDROGENASE, NAD(+)-DEPENDENT; SSADH
ARG1 GDB:1190066q23-6q23 6q22.3-6q23.1 ARGININEMIA
AS GDB:1356976p21.3-6p21.3 ANKYLOSING SPONDYLITIS; AS
ASSP2 GDB:1190176pter-6qter CITRULLINEMIA
BCKDHB GDB:1187596p22-6p21 MAPLE SYRUP URINE DISEASE, TYPE IB
BF GDB:1197266p21.3-6p21.3 GLYCINE-RICH BETA-GLYCOPROTEIN; GBG
C2 GDB:1197316p21.3-6p21.3 COMPLEMENT COMPONENT-2, DEFICIENCY OF
C4A GDB:1197326p21.3-6p21.3 COMPLEMENT COMPONENT 4A; C4A
CDKN1A GDB:2665506p21.2-6p21.2 CYCLIN-DEPENDENT KINASE INHIBITOR 1A; CDKN1A
COL10A1 GDB:1286356q21-6q22 COLLAGEN, TYPE X, ALPHA 1; COL10A1
COL11A2 GDB:1197886p21.3-6p21.3 COLLAGEN, TYPE XI, ALPHA-2; COL11A2
STICKLER SYNDROME, TYPE II; STL2
CYP21A2 GDB:1206056p21.3-6p21.3 ADRENAL HYPERPLASIA, CONGENITAL, DUE TO 21-HYDROXYLASE DEFICIENCY
DYX2 GDB:4375846p22-6p21.3 6p21.3-6p21.3 DYSLEXIA, SPECIFIC, 2; DYX2
EJM1 GDB:1198646p21.1-6p11 6p21.2-6q13 MYOCLONIC EPILEPSY, JUVENILE; EJM1
EPM2A GDB:37633316q23-6q25 6q23.3-6q25 EPILEPSY, PROGRESSIVE MYOCLONIC 2; EPM2
ESR1 GDB:1191206q25.1-6q25.1 ESTROGEN RECEPTOR; ESR
F13A1 GDB:1206146p25.1-6p24.3 FACTOR XIII, A1 SUBUNIT; F13A1
GJA1 GDB:1251966q21-6q23.2 GAP JUNCTION PROTEIN, ALPHA-1, 43 KD; GJA1
GLCLC GDB:1329156p12-6p12 GAMMA-GLUTAMYLCYSTEINE SYNTHETASE DEFICIENCY, HEMOLYTIC ANEMIA DUE
GLYS1 GDB:1364216p21.3-6p21.3 GLYCOSURIA, RENAL
GMPR GDB:1270586p23-6p23 6pter-6qter GUANINE MONOPHOSPHATE REDUCTASE
GSE GDB:99562356p-6p DISEASE; CD
HCR GDB:99933066p21.3-6p21.3 PSORIASIS, SUSCEPTIBILITY TO
HFE GDB:1193096p22-6p22 6p22.1-6p21.3 HEMOCHROMATOSIS; HFE
HLA-A GDB:1193106p21.3-6p21.3 HLA-A HISTOCOMPATIBILITY TYPE; HLAA
HLA-DPB1 GDB:1206366p21.3-6p21.3 HLA-DP HISTOCOMPATIBILITY TYPE, BETA-1 SUBUNIT
HLA-DRA GDB:1206416p21.3-6p21.3 HLA-DR HISTOCOMPATIBILITY TYPE; HLA-DRA
HPFH GDB:98490066q23-6q23 HETEROCELLULAR HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN
ICS1 GDB:1364336p21.3-6p21.3 IMMOTILE CILIA SYNDROME-1; ICS1
IFNGR1 GDB:1206886q23-6q24 6q24.1-6q24.2 INTERFERON, GAMMA, RECEPTOR-1; IFNGR1
IGAD1 GDB:69290776p21.3-6p21.3 SELECTIVE DEFICIENCY OF
IGF2R GDB:1200836q26-6q26 6q25.3-6q25.3 INSULIN-LIKE GROWTH FACTOR 2 RECEPTOR; IGF2R
ISCW GDB:99561586p21.3-6p21.3 SUPPRESSION; IS
LAMA2 GDB:1323626q22-6q23 LAMININ, ALPHA 2; LAMA2
LAP GDB:99589926p21.3-6p21.2 LARYNGEAL ADDUCTOR PARALYSIS; LAP
LPA GDB:1206996q26-6q27 APOLIPOPROTEIN(a); LPA
MCDR1 GDB:1314066q14-6q16.2 MACULAR DYSTROPHY, RETINAL, 1, NORTH CAROLINA TYPE; MCDR1
MOCS1 GDB:98622356p21.3-6p21.3 MOLYBDENUM COFACTOR DEFICIENCY
MUT GDB:1202046p21.2-6p21.1 METHYLMALONICACIDURIA DUE TO METHYLMALONIC CoA MUTASE DEFICIENCY
MYB GDB:1194416q22-6q22 6q23.3-6q24 V-MYB AVIAN MYELOBLASTOSIS VIRAL ONCOGENE HOMOLOG; MYB
NEU1 GDB:12023010pter-10q23 6p21-6p21 6pter-6qter 6p21.3-6p21.3 NEURAMINIDASE DEFICIENCY
NKS1 GDB:1281006p21.3-6p21.3 SUSCEPTIBILITY TO LYSIS BY ALLOREACTIVE NATURAL KILLER CELLS; EC1
NYS2 GDB:98487636p12-6p12 NYSTAGMUS, CONGENITAL
OA3 GDB:1364296q13-6q15 ALBINISM, OCULAR, AUTOSOMAL RECESSIVE; OAR
ODDD GDB:63925846q22-6q24 OCULODENTODIGITAL DYSPLASIA; ODDD
OFC1 GDB:1202476p24-6p24 6p23-6p23 OROFACIAL CLEFT 1; OFC1
PARK2 GDB:68027426q25.2-6q27 PARKINSONISM, JUVENILE
PBCA GDB:99563216pter-6qter BETA CELL AGENESIS WITH NEONATAL DIABETES MELLITUS
PDB1 GDB:1363496p21.3-6p21.3 DISEASE OF BONE; PDB
PEX6 GDB:55924146p22-6p11 PEROXIN-6; PEX6
PEX7 GDB:61558036q22-6q24 RHIZOMELIC CHONDRODYSPLASIA PUNCTATA; RCDP
PEROXIN-7; PEX7
PKHD1 GDB:4339106p21.2-6p12 POLYCYSTIC KIDNEY AND HEPATIC DISEASE-1; PKHD1
PLA2G7 GDB:99588296p21.2-6p12 PLATELET-ACTIVATING FACTOR ACETYLHYDROLASE, SUBUNIT
PLG GDB:1194986q26-6q27 6q26-6q26 PLASMINOGEN; PLG
POLH GDB:69633236p21.1-6p21.1 PIGMENTOSUM WITH NORMAL DNA REPAIR RATES
PPAC GDB:99562486q-6q ARTHROPATHY, PROGRESSIVE PSEUDORHEUMATOID, OF CHILDHOOD
PSORS1 GDB:63813106p21-6p21 6p21.3-6p21.3 PSORIASIS, SUSCEPTIBILITY TO
PUJO GDB:99562316p-6p MULTICYSTIC RENAL DYSPLASIA, BILATERAL; MRD
RCD1 GDB:3339296q26-6q26 RETINAL CONE DEGENERATION
RDS GDB:1188636p21.2-6cen 6p21.1-6cen RETINAL DEGENERATION, SLOW; RDS
RHAG GDB:1360116p21-6qter RHESUS BLOOD GROUP-ASSOCIATED GLYCOPROTEIN; RHAG
RH-NULL, REGULATOR TYPE; RHN
RP14 GDB:4337136p21.3-6p21.2 6p21.3-6p21.3 RETINITIS PIGMENTOSA-14; RP14
TUBBY-LIKE PROTEIN 1; TULP1
RUNX2 GDB:3920826p21-6p21 6p21.1-6p12.3 6p21.2-6p21.1 CLEIDOCRANIAL DYSPLASIA; CCD
CORE-BINDING FACTOR, RUNT DOMAIN, ALPHA SUBUNIT 1; CBFA1
RWS GDB:99561956p21.3-6p21.3 SENSITIVITY
SCA1 GDB:1195886p23-6p23 SPINOCEREBELLAR ATAXIA 1; SCA1
SCZD3 GDB:6359746p24-6p22 DISORDER-3; SCZD3
SIASD GDB:4335526q14-6q15 SIALIC ACID STORAGE DISEASE; SIASD
SOD2 GDB:1195976q25.2-6q25.2 6q25.3-6q25.3 SUPEROXIDE DISMUTASE 2, MITOCHONDRIAL; SOD2
ST8 GDB:61184566q26-6q27 OVARIAN TUMOR
STGD3 GDB:6420556q13-6q13 STARGARDT DISEASE 3; STGD3
TNDM GDB:99562656q22-6q23 DIABETES MELLITUS, TRANSIENT NEONATAL
TNF GDB:1204416p21.3-6p21.3 TUMOR NECROSIS FACTOR; TNF
TPBG GDB:1255686q14-6q15 TROPHOBLAST GLYCOPROTEIN; TPBG; M6P1
TPMT GDB:2090256p22.3-6p22.3 THIOPURINE S-METHYLTRANSFERASE; TPMT
TULP1 GDB:61993536p21.3-6p21.3 TUBBY-LIKE PROTEIN 1; TULP1