Genes, Locations and Genetic Disorders on Chromosome 14

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
AACT GDB:11895514q32.1-14q32.1 ALPHA-1-ANTICHYMOTRYPSIN; AACT
ACHM1 GDB:13245814pter-14qter COLORBLINDNESS, TOTAL
ARVD1 GDB:37133914q23-14q24 ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1; ARVD1
CBG GDB:12786514q32.1-14q32.1 CORTICOSTEROID-BINDING GLOBULIN; CBG
CMH1 GDB:12517614q11.2-14q13 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 1; CMH1
CTAA1 GDB:26529914q24-14qter CATARACT, ANTERIOR POLAR 1; CTAA1
DAD1 GDB:40750514q11-14q12 DEFENDER AGAINST CELL DEATH; DAD1
DFNB5 GDB:63617614q12-14q13 DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 5; DFNB5
EMAPL GDB:632838514q32-14q32 USHER SYNDROME, TYPE IA; USH1A
GALC GDB:11997014q31-14q31 KRABBE DISEASE
GCH1 GDB:11879814q22.1-14q22.2 DYSTONIA, PROGRESSIVE, WITH DIURNAL VARIATION
GTP CYCLOHYDROLASE I DEFICIENCY
GTP CYCLOHYDROLASE I; GCH1
IGH@ GDB:11873114q32.33-14q32.33 IgA CONSTANT HEAVY CHAIN 1; IGHA1
IMMUNOGLOBULIN: D (DIVERSITY) REGION OF HEAVY CHAIN
IgA CONSTANT HEAVY CHAIN 2; IGHA2
IMMUNOGLOBULIN: J (JOINING) LOCI OF HEAVY CHAIN; IGHJ
IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1
IMMUNOGLOBULIN: VARIABLE REGION OF HEAVY CHAINS--Hv1; IGHV
IgG HEAVY CHAIN LOCUS; IGHG1
IMMUNOGLOBULIN Gm-2; IGHG2
IMMUNOGLOBULIN Gm-3; IGHG3
IMMUNOGLOBULIN Gm-4; IGHG4
IMMUNOGLOBULIN: HEAVY DELTA CHAIN; IGHD
IMMUNOGLOBULIN: HEAVY EPSILON CHAIN; IGHE
IGHC group GDB:999263214q32.33-14q32.33 IgA CONSTANT HEAVY CHAIN 1; IGHA1
IgA CONSTANT HEAVY CHAIN 2; IGHA2
IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1
IgG HEAVY CHAIN LOCUS; IGHG1
IMMUNOGLOBULIN Gm-2; IGHG2
IMMUNOGLOBULIN Gm-3; IGHG3
IMMUNOGLOBULIN Gm-4; IGHG4
IMMUNOGLOBULIN: HEAVY DELTA CHAIN; IGHD
IMMUNOGLOBULIN: HEAVY EPSILON CHAIN; IGHE
IGHG1 GDB:12008514q32.33-14q32.33 IgG HEAVY CHAIN LOCUS; IGHG1
IGHM GDB:12008614q32.33-14q32.33 IMMUNOGLOBULIN: HEAVY Mu CHAIN; Mu1; IGHM1
IGHR GDB:995452914q32.33-14q32.33 G1(A1) SYNDROME
IV GDB:13927414q32-14q32 INVERSUS VISCERUM
LTBP2 GDB:45389014q24-14q24 LATENT TRANSFORMING GROWTH FACTOR-BETA BINDING PROTEIN 2; LTBP2
MCOP GDB:995452714q32-14q32 MICROPHTHALMOS
MJD GDB:11884014q21-14q21 14q32.1-14q32.1 MACHADO-JOSEPH DISEASE; MJD
MNG1 GDB:654006214q-14q GOITER, MULTINODULAR 1; MNG1
MPS3C GDB:995453214pter-14qter MUCOPOLYSACCHARIDOSIS TYPE IIIC
MYH6 GDB:12021414q11.2-14q13 14q12-14q12 MYOSIN, HEAVY POLYPEPTIDE 6; MYH6
MYH7 GDB:12021514q11.2-14q12 14q12-14q12 MYOSIN, CARDIAC, HEAVY CHAIN, BETA; MYH7
NP GDB:12023914q11.2-14q11.2 14q13.1-14q13.1 NUCLEOSIDE PHOSPHORYLASE; NP
PABP2 GDB:56713514q11.2-14q13 OCULOPHARYNGEAL MUSCULAR DYSTROPHY; OPMD
OCULOPHARYNGEAL MUSCULAR DYSTROPHY, AUTOSOMAL RECESSIVE
POLYADENYLATE-BINDING PROTEIN-2; PABP2
PI GDB:12028914q32.1-14q32.1 PROTEASE INHIBITOR 1; PI
PSEN1 GDB:13568214q24.3-14q24.3 ALZHEIMER DISEASE, FAMILIAL, TYPE 3; AD3
PYGL GDB:12032814q21-14q21 GLYCOGEN STORAGE DISEASE VI
SLC7A7 GDB:986303314q11.2-14q11.2 DIBASICAMINOACIDURIA II
SPG3A GDB:23012614q12-14q21 SPASTIC PARAPLEGIA-3, AUTOSOMAL DOMINANT; SPG3A
SPTB GDB:11960214q23-14q23 14q22-14q23.2 SPECTRIN, BETA, ERYTHROCYTIC; SPTB
TCL1A GDB:25078514q32.1-14q32.1 T-CELL LYMPHOMA OR LEUKEMIA
TCRAV17S1 GDB:64213014q11.2-14q11.2 T-CELL ANTIGEN RECEPTOR, ALPHA SUBUNIT; TCRA
TCRAV5S1 GDB:45196614q11.2-14q11.2 T-CELL ANTIGEN RECEPTOR, ALPHA SUBUNIT; TCRA
TGM1 GDB:12529914q11.2-14q11.2 TRANSGLUTAMINASE 1; TGM1
ICHTHYOSIS CONGENITA
TITF1 GDB:13258814q13-14q13 THYROID TRANSCRIPTION FACTOR 1; TITF1
TMIP GDB:995452314q13-14q13 AND ULNA, DUPLICATION OF, WITH ABSENCE OF TIBIA AND RADIUS
TRA@ GDB:12040414q11.2-14q11.2 T-CELL ANTIGEN RECEPTOR, ALPHA SUBUNIT; TCRA
TSHR GDB:12531314q31-14q31 THYROTROPIN, UNRESPONSIVENESS TO
USH1A GDB:11888514q32-14q32 USHER SYNDROME, TYPE IA; USH1A
VP GDB:12049214q31-14q32 PORPHYRIA VARIEGATA