Genes, Locations and Genetic Disorders on Chromosome 5

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ADRB2 GDB:1205415q31-5q32 5q32-5q34 BETA-2-ADRENERGIC RECEPTOR; ADRB2
AMCN GDB:98368235q35-5q35 ARTHROGRYPOSIS MULTIPLEX CONGENITA, NEUROGENIC TYPE
APC GDB:1196825q21-5q22 5q22.1-5q22.1 ADENOMATOUS POLYPOSIS OF THE COLON; APC
ARSB GDB:1190085p11-5q13 5q11-5q13 MUCOPOLYSACCHARIDOSIS TYPE VI; MPS VI
BHR1 GDB:99560785q31-5q33 ASTHMA
C6 GDB:1190455p14-5p12 5p13-5p13 COMPLEMENT COMPONENT-6, DEFICIENCY OF
C7 GDB:1190465p14-5p12 5p13-5p13 COMPLEMENT COMPONENT-7, DEFICIENCY OF
CCAL2 GDB:55842655p15.2-5p15.1 CHONDROCALCINOSIS, FAMILIAL ARTICULAR
CKN1 GDB:1285865pter-5qter COCKAYNE SYNDROME, TYPE I; CKN1
CMDJ GDB:95954255p15.2-5p14.1 CRANIOMETAPHYSEAL DYSPLASIA, JACKSON TYPE; CMDJ
CRHBP GDB:1274385q-5q 5q12-5q13.3 5q12-5q13.3 CORTICOTROPIN RELEASING HORMONE-BINDING PROTEIN; CRHBP
CSF1R GDB:1206005q33.3-5q34 5q33.2-5q33.3 COLONY-STIMULATING FACTOR-1 RECEPTOR; CSF1R
DHFR GDB:1198455q11.2-5q13.2 5q12-5q14 DIHYDROFOLATE REDUCTASE; DHFR
DIAPH1 GDB:98354825q31-5q31 DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 1; DFNA1
DIAPHANOUS, DROSOPHILA, HOMOLOG OF, 1
DTR GDB:1198535q23-5q23 DIPHTHERIA TOXIN SENSITIVITY; DTS
EOS GDB:99560835q31-5q33 EOSINOPHILIA, FAMILIAL
ERVR GDB:98358575q13-5q14 HYALOIDEORETINAL DEGENERATION OF WAGNER
F12 GDB:1198925q33-5qter 5q34-5qter HAGEMAN FACTOR DEFICIENCY
FBN2 GDB:1281225q21-5q33 5q23-5q31 CONTRACTURAL ARACHNODACTYLY, CONGENITAL; CCA
GDNF GDB:4506095p13.3-5p13.1 GLIAL CELL LINE-DERIVED NEUROTROPHIC FACTOR; GDNF
GHR GDB:1199845p14-5p12 5p13-5p12 GROWTH HORMONE RECEPTOR; GHR
GLRA1 GDB:1188015q32-5q32 GLYCINE RECEPTOR, ALPHA-1 SUBUNIT; GLRA1
GM2A GDB:1200005q32-5q33 5q31.3-5q33.1 TAY-SACHS DISEASE, AB VARIANT
HEXB GDB:1193085q13-5q13 SANDHOFF DISEASE
HSD17B4 GDB:3850595q2-5q2 17-@BETA-HYDROXYSTEROID DEHYDROGENASE IV; HSD17B4
ITGA2 GDB:1280315q23-5q31 5q11.1-5q11.2 INTEGRIN, ALPHA-2; ITGA2
KFS GDB:99589875q11.2-5q11.2 VERTEBRAL FUSION
LGMD1A GDB:1188325q22-5q34 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 1A; LGMD1A
LOX GDB:1193675q23.3-5q31.2 LYSYL OXIDASE; LOX
LTC4S GDB:3840805q35-5q35 LEUKOTRIENE C4 SYNTHASE; LTC4S
MAN2A1 GDB:1364135q21-5q22 MANNOSIDASE, ALPHA, II; MANA2
DYSERYTHROPOIETIC ANEMIA, CONGENITAL, TYPE II
MCC GDB:1281635q21-5q22 5q21-5q21 5q22.1-5q22.1 MUTATED IN COLORECTAL CANCERS; MCC
MSH3 GDB:6419865q11-5q12 5q11.2-5q14 5q11.2-5q13.2 MutS, E. COLI, HOMOLOG OF, 3; MSH3
MSX2 GDB:1387665q34-5q35 MSH (DROSOPHILA) HOMEO BOX HOMOLOG 2; MSX2
NR3C1 GDB:1200175q31-5q32 5q31-5q31 GLUCOCORTICOID RECEPTOR; GRL
PCSK1 GDB:1280335q15-5q21 PROPROTEIN CONVERTASE SUBTILISIN/KEXIN TYPE 1; PCSK1
PDE6A GDB:1202655q31-5q33 5q31.2-5q34 PHOSPHODIESTERASE 6A, cGMP-SPECIFIC, ROD, ALPHA; PDE6A
PFBI GDB:99560965q31-5q33 INTENSITY OF INFECTION IN
RASA1 GDB:1203395q13-5q13 5q13.3-5q13.3 RAS p21 PROTEIN ACTIVATOR 1; RASA1
SCZD1 GDB:1203705q11.2-5q13.3 DISORDER-1; SCZD1
SDHA GDB:3780375p15-5p15 SUCCINATE DEHYDROGENASE COMPLEX, SUBUNIT A, FLAVOPROTEIN; SDHA
SGCD GDB:58864215q33-5q34 SARCOGLYCAN, DELTA; SGCD
SLC22A5 GDB:98632775q31-5q31 5q31.1-5q32 CARNITINE DEFICIENCY, SYSTEMIC, DUE TO DEFECT IN RENAL REABSORPTION
SLC26A2 GDB:1254215q31-5q34 5q32-5q33.1 DIASTROPHIC DYSPLASIA; DTD
SM1 GDB:98344885q31-5q33 SCHISTOSOMA MANSONI SUSCEPTIBILITY/RESISTANCE
SMA@ GDB:1203785q12.2-5q13 SPINAL MUSCULAR ATROPHY I; SMA I
SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1
SMN1 GDB:52151735q13-5q13 SPINAL MUSCULAR ATROPHY I; SMA I
SURVIVAL OF MOTOR NEURON 1, TELOMERIC; SMN1
SMN2 GDB:52151755q13-5q13 SPINAL MUSCULAR ATROPHY I; SMA I
SURVIVAL OF MOTOR NEURON 2, CENTROMERIC; SMN2
TCOF1 GDB:1273905q32-5q33.1 TREACHER COLLINS-FRANCESCHETTI SYNDROME 1; TCOF1
TGFBI GDB:5976015q31-5q31 CORNEAL DYSTROPHY, GRANULAR TYPE
CORNEAL DYSTROPHY, LATTICE TYPE I; CDL1
TRANSFORMING GROWTH FACTOR, BETA-INDUCED, 68 KD; TGFBI