Genes, Locations and Genetic Disorders on Chromosome 4

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ADH2 GDB:1196514q21-4q23 4q22-4q22 ALCOHOL DEHYDROGENASE-2; ADH2
ADH3 GDB:1196524q21-4q23 4q22-4q22 ALCOHOL DEHYDROGENASE-3; ADH3
AFP GDB:1196604q11-4q13 ALPHA-FETOPROTEIN; AFP
AGA GDB:1189814q23-4q35 4q32-4q33 ASPARTYLGLUCOSAMINURIA; AGU
AIH2 GDB:1187514q11-4q13 AMELOGENESIS IMPERFECTA 2, HYPOPLASTIC LOCAL, AUTOSOMAL DOMINANT;
ALB GDB:1189904q11-4q13 ALBUMIN; ALB
ASMD GDB:1197054q-4q 4q28-4q31 ANTERIOR SEGMENT OCULAR DYSGENESIS; ASOD
CNGA1 GDB:1275574p14-4q13 CYCLIC NUCLEOTIDE GATED CHANNEL, PHOTORECEPTOR, cGMP GATED, 1; CNCG1
CRBM GDB:99581324p16.3-4p16.3 CHERUBISM
DCK GDB:1268104q13.3-4q21.1 DEOXYCYTIDINE KINASE; DCK
DGI1 GDB:1190924q12-4q23 DENTINOGENESIS IMPERFECTA; DGI1
DSPP GDB:55604574pter-4qter 4q21.3-4q21.3 DENTIN PHOSPHOPROTEIN; DPP
DTDP2 GDB:99558104q-4q DENTIN DYSPLASIA, TYPE II
ETFDH GDB:1359924q32-4q35 GLUTARICACIDURIA IIC; GA IIC
EVC GDB:5555734p16-4p16 ELLIS-VAN CREVELD SYNDROME; EVC
F11 GDB:1198914q35-4q35 PTA DEFICIENCY
FABP2 GDB:1191274q28-4q31 FATTY ACID BINDING PROTEIN 2, INTESTINAL; FABP2
FGA GDB:1191294q28-4q28 FIBRINOGEN, A ALPHA POLYPEPTIDE; FGA
FGB GDB:1191304q28-4q28 FIBRINOGEN, B BETA POLYPEPTIDE; FGB
FGFR3 GDB:1275264p16.3-4p16.3 ACHONDROPLASIA; ACH
FIBROBLAST GROWTH FACTOR RECEPTOR-3; FGFR3
FGG GDB:1191324q28-4q28 FIBRINOGEN, G GAMMA POLYPEPTIDE; FGG
FSHMD1A GDB:1199144q35-4q35 FACIOSCAPULOHUMERAL MUSCULAR DYSTROPHY 1A; FSHMD1A
GC GDB:1192634q12-4q13 4q12-4q12 GROUP-SPECIFIC COMPONENT; GC
GNPTA GDB:1192804q21-4q23 MUCOLIPIDOSIS II; ML2; ML II
GNRHR GDB:1364564q13-4q13 4q21.2-4q21.2 GONADOTROPIN-RELEASING HORMONE RECEPTOR; GNRHR
GYPA GDB:1188904q28-4q31 4q28.2-4q31.1 BLOOD GROUP--MN LOCUS; MN
HCA GDB:99546754q33-4qter HYPERCALCIURIA, FAMILIAL IDIOPATHIC
HCL2 GDB:1193054q28-4q31 4q-4q HAIR COLOR-2; HCL2
HD GDB:1193074p16.3-4p16.3 HUNTINGTON DISEASE; HD
HTN3 GDB:1256014q12-4q21 HISTATIN-3; HTN3
HVBS6 GDB:1206874q32-4q32 HEPATOCELLULAR CARCINOMA-2; HCC2
IDUA GDB:1193274p16.3-4p16.3 MUCOPOLYSACCHARIDOSIS TYPE I; MPS I
IF GDB:1200774q24-4q25 4q25-4q25 COMPLEMENT COMPONENT-3 INACTIVATOR, DEFICIENCY OF
JPD GDB:1201134pter-4qter 4q12-4q13 PERIODONTITIS, JUVENILE; JPD
KIT GDB:1201174q12-4q12 V-KIT HARDY-ZUCKERMAN 4 FELINE SARCOMA VIRAL ONCOGENE HOMOLOG; KIT
KLKB1 GDB:1275754q34-4q35 4q35-4q35 FLETCHER FACTOR DEFICIENCY
LQT4 GDB:6820724q25-4q27 SYNDROME WITHOUT PSYCHOMOTOR RETARDATION
MANBA GDB:1252614q21-4q25 MANNOSIDOSIS, BETA; MANB1
MLLT2 GDB:1367924q21-4q21 MYELOID/LYMPHOID OR MIXED LINEAGE LEUKEMIA, TRANSLOCATED TO, 2; MLLT2
MSX1 GDB:1206834p16.3-4p16.1 4p16.1-4p16.1 MSH, DROSOPHILA, HOMEO BOX, HOMOLOG OF, 1; MSX1
MTP GDB:2289614q24-4q24 MICROSOMAL TRIGLYCERIDE TRANSFER PROTEIN, 88 KD; MTP
NR3C2 GDB:1201884q31-4q31 4q31.1-4q31.1 PSEUDOHYPOALDOSTERONISM, TYPE I, AUTOSOMAL RECESSIVE; PHA1
PBT GDB:1202604q12-4q21 PIEBALD TRAIT; PBT
PDE6B GDB:1259154p16.3-4p16.3 NIGHTBLINDNESS, CONGENITAL STATIONARY; CSNB3
PHOSPHODIESTERASE 6B, cGMP-SPECIFIC, ROD, BETA; PDE6B
PEE1 GDB:70167654q31-4q34 4q25-4qter 1; PEE1
PITX2 GDB:1347704q25-4q27 4q25-4q26 4q25-4q25 IRIDOGONIODYSGENESIS, TYPE 2; IRID2
RIEGER SYNDROME, TYPE 1; RIEG1
RIEG BICOID-RELATED HOMEOBOX TRANSCRIPTION FACTOR 1; RIEG1
HOMEO BOX 2
PKD2 GDB:1188514q21-4q23 POLYCYSTIC KIDNEY DISEASE 2; PKD2
QDPR GDB:1203314p15.3-4p15.3 4p15.31-4p15.31 PHENYLKETONURIA II
SGCB GDB:7020724q12-4q12 MUSCULAR DYSTROPHY, LIMB-GIRDLE, TYPE 2E; LGMD2E
SNCA GDB:4390474q21.3-4q22 4q21-4q21 SYNUCLEIN, ALPHA; SNCA
PARKINSON DISEASE, FAMILIAL, TYPE 1; PARK1
SOD3 GDB:1252914p16.3-4q21 SUPEROXIDE DISMUTASE, EXTRACELLULAR; SOD3
STATH GDB:1203914q11-4q13 STATHERIN; STATH; STR
TAPVR1 GDB:3926464p13-4q11 ANOMALOUS PULMONARY VENOUS RETURN; APVR
TYS GDB:1196244q-4q SCLEROTYLOSIS; TYS
WBS2 GDB:1324264q33-4q35.1 WILLIAMS-BEUREN SYNDROME; WBS
WFS1 GDB:4342944p-4p 4p16-4p16 DIABETES MELLITUS AND INSIPIDUS WITH OPTIC ATROPHY AND DEAFNESS
WHCR GDB:1253554p16.3-4p16.3 WOLF-HIRSCHHORN SYNDROME; WHS