Genes, Locations and Genetic Disorders on Chromosome 7

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ABCB1 GDB:1207127q21-7q21 7q21.1-7q21.1 P-GLYCOPROTEIN-1; PGY1
ABCB4 GDB:1207137q21-7q21 7q21.1-7q21.1 P-GLYCOPROTEIN-3; PGY3
ACHE GDB:1187467q22-7q22 ACETYLCHOLINESTERASE
AQP1 GDB:1290827p14-7p14 AQUAPORIN-1; AQP1
ASL GDB:1197037q21.3-7q22 7cen-7q11.2 ARGININOSUCCINICACIDURIA
ASNS GDB:1197067q21-7q31 ASPARAGINE SYNTHETASE; ASNS; AS
AUTS1 GDB:98642267q32-7q34 DISORDER
BCP GDB:1190327q31.3-7q32 TRITANOPIA
BPGM GDB:1190397q31-7q34 DIPHOSPHOGLYCERATE MUTASE DEFICIENCY OF ERYTHROCYTE
CACNA2D1 GDB:1320107q21-7q22 CALCIUM CHANNEL, VOLTAGE-DEPENDENT, L TYPE, ALPHA-2/DELTA SUBUNIT;
MALIGNANT HYPERTHERMIA SUSCEPTIBILITY-3
CCM1 GDB:5808247q11.2-7q21 CEREBRAL CAVERNOUS MALFORMATIONS 1; CCM1
CD36 GDB:1388007q11.2-7q11.2 CD36 ANTIGEN; CD36
CFTR GDB:1205847q31.3-7q31.3 7q31.2-7q31.3 7q31.2-7q31.2 CYSTIC FIBROSIS; CF
DEFERENS, CONGENITAL BILATERAL APLASIA OF; CBAVD; CAVD
CLCN1 GDB:1346887q32-7qter CHLORIDE CHANNEL 1, SKELETAL MUSCLE; CLCN1
CLD GDB:1382737q31-7q31 CHLORIDE DIARRHEA, FAMILIAL; CLD
CMH6 GDB:99563927q3-7q3 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, WITH WOLFF-PARKINSON-WHITE
CMT2D GDB:99532327p14-7p14 CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, D
COL1A2 GDB:1190627q21.3-7q22.1 7q22.1-7q22.1 COLLAGEN, TYPE I, ALPHA-2 POLYPEPTIDE; COL1A2
OSTEOGENESIS IMPERFECTA TYPE I
CRS GDB:1190737p21-7p21 CRANIOSYNOSTOSIS, TYPE 1; CRS1
CYMD GDB:3665947p21-7p15 MACULAR EDEMA, CYSTOID
DFNA5 GDB:6361747p15-7p15 DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 5; DFNA5
DLD GDB:1206087q31-7q32 LIPOAMIDE DEHYDROGENASE DEFICIENCY, LACTIC ACIDOSIS DUE TO
DRA GDB:1381657q22-7q31.1 DOWN-REGULATED IN ADENOMA; DRA
EEC1 GDB:1363387q11.2-7q21.3 ECTRODACTYLY, ECTODERMAL DYSPLASIA, AND CLEFT LIP/PALATE; EEC
ELN GDB:1191077q11.23-7q11.23 ELASTIN; ELN
WILLIAMS-BEUREN SYNDROME; WBS
ETV1 GDB:3352297p22-7p22 ETS VARIANT GENE 1; ETV1
GCK GDB:1275507p-7p 7p15-7p13 DIABETES MELLITUS, AUTOSOMAL DOMINANT, TYPE II
GHRHR GDB:1384657p14-7p14 GROWTH HORMONE-RELEASING HORMONE RECEPTOR; GHRHR
GHS GDB:99563637p-7p MICROSOMIA WITH RADIAL DEFECTS
GLI3 GDB:1199907p13-7p13 PALLISTER-HALL SYNDROME; PHS
GLI-KRUPPEL FAMILY MEMBER 3; GLI3
POSTAXIAL POLYDACTYLY, TYPE A1
GREIG CEPHALOPOLYSYNDACTYLY SYNDROME; GCPS
GPDS1 GDB:99564107q35-7q36 GLAUCOMA, PIGMENT-DISPERSION TYPE
GUSB GDB:1200257q11.21-7q11.22 7q21.11-7q21.11 7q22-7q22 MUCOPOLYSACCHARIDOSIS TYPE VII
HADH GDB:1200337pter-7qter HYDROXYACYL-CoA DEHYDROGENASE/3-KETOACYL-CoA THIOLASE/ENOYL-CoA HYDRATASE,
HLXB9 GDB:1364111q41-1q42.1 7q36-7q36 HOMEO BOX GENE HB9; HLXB9
SACRAL AGENESIS, HEREDITARY, WITH PRESACRAL MASS, ANTERIOR MENINGOCELE,
HOXA13 GDB:1206567p15-7p14 7p15.3-7p15.3 HOMEO BOX A13; HOXA13
HPFH2 GDB:1280717q36-7q36 HEREDITARY PERSISTENCE OF FETAL HEMOGLOBIN, HETEROCELLULAR, INDIAN
HRX GDB:99589997q-7q HRX
KCNH2 GDB:1381267q35-7q36 LONG QT SYNDROME, TYPE 2; LQT2
LAMB1 GDB:1193577q22-7q22 7q31.1-7q31.3 LAMININ BETA 1; LAMB1
LEP GDB:1364207q31.3-7q31.3 7q32.1-7q32.1 LEPTIN; LEP
MET GDB:1201787q31-7q31 7q31.2-7q31.3 MET PROTO-ONCOGENE; MET
NCF1 GDB:1202227q11.23-7q11.23 GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-POSITIVE FORM
NM GDB:1194547q22-7qter NEUTROPHIL CHEMOTACTIC RESPONSE; NCR
OGDH GDB:1188477p13-7p11.2 7p14-7p13 ALPHA-KETOGLUTARATE DEHYDROGENASE DEFICIENCY
OI4 GDB:1194647q21.3-7q22.1 OSTEOGENESIS IMPERFECTA TYPE IV; OI4
PAI1 GDB:1202977q22.1-7q22.3 PLASMINOGEN ACTIVATOR INHIBITOR, TYPE I; PAI1
PDS GDB:55845117q21-7q34 7q31-7q31 PENDRED SYNDROME; PDS
DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 4; DFNB4
PEX1 GDB:97871107q21-7q22 PEROXIN-1; PEX1
PGAM2 GDB:1202807p13-7p12 7p13-7p12.3 PHOSPHOGLYCERATE MUTASE, DEFICIENCY OF M SUBUNIT OF
PMS2 GDB:3864067p22-7p22 POSTMEIOTIC SEGREGATION INCREASED (S. CEREVISIAE)-2; PMS2
PON1 GDB:1203087q21-7q22 PARAOXONASE 1; PON1
PRSS1 GDB:1196207q32-7qter 7q35-7q35 PANCREATITIS, HEREDITARY; PCTT
PROTEASE, SERINE, 1; PRSS1
PTC GDB:1187447q-7q 7q33-7q33 PHENYLTHIOCARBAMIDE TASTING
PTPN12 GDB:1368467q11.23-7q11.23 PROTEIN-TYROSINE PHOSPHATASE, NONRECEPTOR TYPE, 12; PTPN12
RP10 GDB:1387867q-7q 7q31-7q33 7q31-7q32 RETINITIS PIGMENTOSA-10; RP10
RP9 GDB:3339317p-7p RETINITIS PIGMENTOSA-9; RP9
SHFM1 GDB:1281957q21.3-7q22.1 SPLIT-HAND/FOOT DEFORMITY, TYPE I; SHFD1
SHH GDB:4563097q36-7q36 HOLOPROSENCEPHALY, TYPE 3; HPE3
SONIC HEDGEHOG, DROSOPHILA, HOMOLOG OF; SHH
SLOS GDB:3859507q32-7q32 7q32.1-7q32.1 SMITH-LEMLI-OPITZ SYNDROME
SMAD1 GDB:37633457p14-7p14 7pter-7pter 7p15.2-7p14.3 SPINAL MUSCULAR ATROPHY, DISTAL, WITH UPPER LIMB PREDOMINANCE; SMAD1
TBXAS1 GDB:1287447q34-7q35 7q33-7q34 THROMBOXANE A SYNTHASE 1; TBXAS1
TWIST GDB:1356947p21.2-7p21.2 ACROCEPHALOSYNDACTYLY TYPE III
TWIST, DROSOPHILA, HOMOLOG OF; TWIST
ZWS1 GDB:1205117q11-7q11 ZELLWEGER SYNDROME; ZS