Genes, Locations and Genetic Disorders on Chromosome 3

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ACAA1 GDB:1196433p23-3p22 PEROXISOMAL 3-OXOACYL-COENZYME A THIOLASE DEFICIENCY
AGTR1 GDB:1323593q21-3q25 ANGIOTENSIN II RECEPTOR, VASCULAR TYPE 1; AT2R1
AHSG GDB:1189853q27-3q27 ALPHA-2-HS-GLYCOPROTEIN; AHSG
AMT GDB:1321383p21.3-3p21.2 3p21.2-3p21.1 HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE II; NKH2
ARP GDB:99590493p21.1-3p21.1 ARGININE-RICH PROTEIN
BBS3 GDB:3765013p-3p 3p12.3-3q11.1 BARDET-BIEDL SYNDROME, TYPE 3; BBS3
BCHE GDB:1205583q26.1-3q26.2 BUTYRYLCHOLINESTERASE; BCHE
BCPM GDB:4338093q21-3q21 BENIGN CHRONIC PEMPHIGUS; BCPM
BPES GDB:1290253q22-3q23 BLEPHAROPHIMOSIS, EPICANTHUS INVERSUS, AND PTOSIS; BPES
BTD GDB:3090783p25-3p25 BIOTINIDASE; BTD
CACT GDB:65032973p21.31-3p21.31 CARNITINE-ACYLCARNITINE TRANSLOCASE; CACT
CASR GDB:1341963q21-3q24 HYPOCALCIURIC HYPERCALCEMIA, FAMILIAL; HHC1
CCR2 GDB:3373643p21-3p21 CHEMOKINE (C-C) RECEPTOR 2; CMKBR2
CCR5 GDB:12305103p21-3p21 CHEMOKINE (C-C) RECEPTOR 5; CMKBR5
CDL1 GDB:1363443q26.3-3q26.3 DE LANGE SYNDROME; CDL
CMT2B GDB:6040213q13-3q22 CHARCOT-MARIE-TOOTH DISEASE, NEURONAL TYPE, B; CMT2B
COL7A1 GDB:1287503p21-3p21 3p21.3-3p21.3 COLLAGEN, TYPE VII, ALPHA-1; COL7A1
CP GDB:1190693q23-3q25 3q21-3q24 CERULOPLASMIN; CP
CTNNB1 GDB:1419223p22-3p22 3p21.3-3p21.3 CATENIN, BETA 1; CTNNB1
DEM GDB:6811573p12-3q11 DEMENTIA, FAMILIAL NONSPECIFIC; DEM
ETM1 GDB:97325233q13-3q13 TREMOR, HEREDITARY ESSENTIAL 1; ETM1
FANCD GDB:6983453pter-3p24.2 FANCONI PANCYTOPENIA, COMPLEMENTATION GROUP D
FIH GDB:99557903q13-3q13 HYPOPARATHYROIDISM, FAMILIAL ISOLATED; FIH
GBE1 GDB:1384423p12-3p12 GLYCOGEN STORAGE DISEASE IV
GLB1 GDB:1199873p22-3p21.33 3p21.33-3p21.33 GANGLIOSIDOSIS, GENERALIZED GM1, TYPE I
GLC1C GDB:38019413q21-3q24 GLAUCOMA 1, OPEN ANGLE, C; GLC1C
GNAI2 GDB:1205163p21.3-3p21.2 GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-INHIBITING, POLYPEPTIDE-2;
GNAT1 GDB:1192773p21.3-3p21.2 GUANINE NUCLEOTIDE-BINDING PROTEIN, ALPHA-TRANSDUCING, POLYPEPTIDE
GP9 GDB:1263703pter-3qter PLATELET GLYCOPROTEIN IX; GP9
GPX1 GDB:1192823q11-3q12 3p21.3-3p21.3 GLUTATHIONE PEROXIDASE; GPX1
HGD GDB:2039353q21-3q23 ALKAPTONURIA; AKU
HRG GDB:1200553q27-3q27 HISTIDINE-RICH GLYCOPROTEIN; HRG; HRGP
ITIH1 GDB:1201073p21.2-3p21.1 INTER-ALPHA-TRYPSIN INHIBITOR, HEAVY CHAIN-1; ITIH1; IATIH; ITIH
KNG GDB:1252563q27-3q27 FLAUJEAC FACTOR DEFICIENCY
LPP GDB:13917953q27-3q28 LIM DOMAIN-CONTAINING PREFERRED TRANSLOCATION PARTNER IN LIPOMA; LPP
LRS1 GDB:6824483p21.1-3p14.1 LARSEN SYNDROME, AUTOSOMAL DOMINANT; LRS1
MDS1 GDB:2504113q26-3q26 MYELODYSPLASIA SYNDROME 1; MDS1
MITF GDB:2147763p14.1-3p12 MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF
WAARDENBURG SYNDROME, TYPE II; WS2
MLH1 GDB:2496173p23-3p22 3p21.3-3p21.3 COLON CANCER, FAMILIAL, NONPOLYPOSIS TYPE 2; FCC2
MYL3 GDB:1202183p21.3-3p21.2 MYOSIN, LIGHT CHAIN, ALKALI, VENTRICULAR AND SKELETAL SLOW; MYL3
OPA1 GDB:1188483q28-3q29 OPTIC ATROPHY 1; OPA1
PBXP1 GDB:1253523q22-3q23 PRE-B-CELL LEUKEMIA TRANSCRIPTION FACTOR-1; PBX1
PCCB GDB:1194743q21-3q22 GLYCINEMIA, KETOTIC, II
POU1F1 GDB:1290703p11-3p11 POU DOMAIN, CLASS 1, TRANSCRIPTION FACTOR 1; POU1F1
PROS1 GDB:1207213p11-3q11 3p11.1-3q11.2 PROTEIN S, ALPHA; PROS1
PTHR1 GDB:1381283p22-3p21.1 PARATHYROID HORMONE RECEPTOR 1; PTHR1
RCA1 GDB:2302333p14.2-3p14.2 RENAL CARCINOMA, FAMILIAL, ASSOCIATED 1; RCA1
RHO GDB:1203473q21.3-3q24 RHODOPSIN; RHO
SCA7 GDB:4544713p21.1-3p12 SPINOCEREBELLAR ATAXIA 7; SCA7
SCLC1 GDB:99557503p23-3p21 SMALL-CELL CANCER OF THE LUNG; SCCL
SCN5A GDB:1321523p21-3p21 SODIUM CHANNEL, VOLTAGE-GATED, TYPE V, ALPHA POLYPEPTIDE; SCN5A
SI GDB:1203773q25.2-3q26.2 DISACCHARIDE INTOLERANCE I
SLC2A2 GDB:1199953q26.2-3q27 3q26.1-3q26.3 SOLUTE CARRIER FAMILY 2, MEMBER 2; SLC2A2
FANCONI-BICKEL SYNDROME; FBS
TF GDB:1204323q21-3q21 TRANSFERRIN; TF
TGFBR2 GDB:2249093p22-3p22 3pter-3p24.2 TRANSFORMING GROWTH FACTOR-BETA RECEPTOR, TYPE II; TGFBR2
THPO GDB:3740073q26.3-3q27 THROMBOPOIETIN; THPO
THRB GDB:1207313p24.1-3p22 3p24.3-3p24.3 THYROID HORMONE RECEPTOR, BETA; THRB
TKT GDB:1324023p14.3-3p14.3 WERNICKE-KORSAKOFF SYNDROME
TM4SF1 GDB:2508153q21-3q25 TUMOR-ASSOCIATED ANTIGEN L6; TAAL6
TRH GDB:1280723pter-3qter THYROTROPIN-RELEASING HORMONE DEFICIENCY
UMPS GDB:1204823q13-3q13 OROTICACIDURIA I
UQCRC1 GDB:1418503p21.3-3p21.2 3p21.3-3p21.3 UBIQUINOL-CYTOCHROME c REDUCTASE CORE PROTEIN I; UQCRC1
USH3A GDB:3926453q21-3q25 USHER SYNDROME, TYPE III; USH3
VHL GDB:1204883p26-3p25 VON HIPPEL-LINDAU SYNDROME; VHL
WS2A GDB:1280533p14.2-3p13 MICROPHTHALMIA-ASSOCIATED TRANSCRIPTION FACTOR; MITF
WAARDENBURG SYNDROME, TYPE II; WS2
XPC GDB:1347693p25.1-3p25.1 XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP C; XPC
ZNF35 GDB:1205073p21-3p21 ZINC FINGER PROTEIN-35; ZNF35