Genes, Locations and Genetic Disorders on Chromosome 16

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ABCC6 GDB:931510616p13.1-16p13.1 PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL DOMINANT; PXE
PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE
ALDOA GDB:11899316q22.2-16q22.2 ALDOLASE A, FRUCTOSE-BISPHOSPHATE; ALDOA
APRT GDB:11900316q24.2-16qter ADENINE PHOSPHORIBOSYLTRANSFERASE; APRT
ATP2A1 GDB:11971616p12.1-16p12.1 ATPase, Ca(2+)-TRANSPORTING, FAST-TWITCH 1; ATP2A1
BRODY MYOPATHY
BBS2 GDB:22999216q21-16q21 BARDET-BIEDL SYNDROME, TYPE 2; BBS2
BLAU GDB:70121516p12-16q21 SYNOVITIS, GRANULOMATOUS, WITH UVEITIS AND CRANIAL NEUROPATHIES
CATM GDB:70121916p13.3-16p13.3 MICROPHTHALMIA-CATARACT
CDH1 GDB:12048416q22.1-16q22.1 CADHERIN 1; CDH1
CETP GDB:11977316q21-16q21 16q13-16q13 CHOLESTERYL ESTER TRANSFER PROTEIN, PLASMA; CETP
CLN3 GDB:12059316p12.1-16p12.1 16p12.1-16p11.2 CEROID-LIPOFUSCINOSIS, NEURONAL 3, JUVENILE; CLN3
CREBBP GDB:43715916p13.3-16p13.3 RUBINSTEIN SYNDROME
CREB-BINDING PROTEIN; CREBBP
CTH GDB:11908616pter-16qter CYSTATHIONINURIA
CTM GDB:11981916q22.1-16q23.1 CATARACT, ZONULAR
CYBA GDB:12523816q24-16q24 GRANULOMATOUS DISEASE, CHRONIC, AUTOSOMAL CYTOCHROME-b-NEGATIVE FORM
CYLD1 GDB:70121616q12-16q13 EPITHELIOMA, HEREDITARY MULTIPLE BENIGN CYSTIC
DHS GDB:995826816q23-16q24 XEROCYTOSIS, HEREDITARY
DNASE1 GDB:13284616p13.3-16p13.3 DEOXYRIBONUCLEASE I; DNASE1
DPEP1 GDB:12805916q24-16q24 16q24.3-16q24.3 RENAL DIPEPTIDASE
ERCC4 GDB:11911316p13.13-16p13.13 EXCISION-REPAIR, COMPLEMENTING DEFECTIVE, IN CHINESE HAMSTER, 4; ERCC4
XERODERMA PIGMENTOSUM, COMPLEMENTATION GROUP F; XPF
FANCA GDB:70122116q24.3-16q24.3 FANCONI ANEMIA, COMPLEMENTATION GROUP A; FACA
GALNS GDB:12908516q24-16q24 MUCOPOLYSACCHARIDOSIS TYPE IVA
GAN GDB:986488516q24.1-16q24.1 NEUROPATHY, GIANT AXONAL; GAN
HAGH GDB:11929216p13.3-16p13.3 HYDROXYACYL GLUTATHIONE HYDROLASE; HAGH
HBA1 GDB:11929316p13.3-16p13.3 HEMOGLOBIN--ALPHA LOCUS-1; HBA1
HBA2 GDB:11929416p13.3-16p13.3 HEMOGLOBIN--ALPHA LOCUS-2; HBA2
HBHR GDB:995454116pter-16p13.3 HEMOGLOBIN H-RELATED MENTAL RETARDATION
HBQ1 GDB:12003616p13.3-16p13.3 HEMOGLOBIN--THETA-1 LOCUS; HBQ1
HBZ GDB:11930216p13.3-16p13.3 HEMOGLOBIN--ZETA LOCUS; HBZ
HBZP GDB:12003716p13.3-16p13.3 HEMOGLOBIN--ZETA LOCUS; HBZ
HP GDB:11931416q22.2-16q22.2 16q22.1-16q22.1 HAPTOGLOBIN; HP
HSD11B2 GDB:40995116q22-16q22 CORTISOL 11-BETA-KETOREDUCTASE DEFICIENCY
IBD1 GDB:986302716p12-16q13 REGIONAL ENTERITIS
IL4R GDB:11882316p12.1-16p12.1 INTERLEUKIN-4 RECEPTOR; IL4R
LIPB GDB:11936516pter-16qter LIPASE B, LYSOSOMAL ACID; LIPB
MC1R GDB:13516216q24.3-16q24.3 MELANOCORTIN-1 RECEPTOR; MC1R
MCDC1 GDB:13140716q22.1-16q23.2 CORNEAL DYSTROPHY, MACULAR TYPE
MEFV GDB:12526316p13.3-16p13.3 MEDITERRANEAN FEVER, FAMILIAL; MEFV
MHC2TA GDB:626847516p13.3-16p13.2 MHC CLASS II TRANSACTIVATOR; MHC2TA
PHKB GDB:12028616q12.1-16q12.1 PHOSPHORYLASE KINASE, BETA SUBUNIT; PHKB
PHKG2 GDB:14031616p11.2-16p11.2 PHOSPHORYLASE KINASE, TESTIS/LIVER, GAMMA 2; PHKG2
PKD1 GDB:12029316p13.3-16p13.3 POLYCYSTIC KIDNEYS
POLYCYSTIC KIDNEY DISEASE 1; PKD1
PKDTS GDB:995454516p13.3-16p13.3 POLYCYSTIC KIDNEY DISEASE, INFANTILE SEVERE, WITH TUBEROUS SCLEROSIS;
PMM2 GDB:43869716p13-16p13 16p13.3-16p13.12 CARBOHYDRATE-DEFICIENT GLYCOPROTEIN SYNDROME, TYPE I; CDG1
PHOSPHOMANNOMUTASE 2; PMM2
PXE GDB:605389516p13.1-16p13.1 PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL DOMINANT; PXE
PSEUDOXANTHOMA ELASTICUM, AUTOSOMAL RECESSIVE; PXE
SALL1 GDB:421616116q12.1-16q12.1 TOWNES-BROCKS SYNDROME; TBS
SAL-LIKE 1; SALL1
SCA4 GDB:25036416q24-16qter SPINOCEREBELLAR ATAXIA 4; SCA4
SCNN1B GDB:43447116p12.2-16p12.1 SODIUM CHANNEL, NONVOLTAGE-GATED 1 BETA; SCNN1B
SCNN1G GDB:56875916p12.2-16p12.1 SODIUM CHANNEL, NONVOLTAGE-GATED 1 GAMMA; SCNN1G
TAT GDB:12039816q22.2-16q22.2 TYROSINE TRANSAMINASE DEFICIENCY
TSC2 GDB:12046616p13.3-16p13.3 TUBEROUS SCLEROSIS-2; TSC2
VDI GDB:11962916pter-16qter DEFECTIVE INTERFERING PARTICLE INDUCTION, CONTROL OF
WT3 GDB:995895716q-16q WILMS TUMOR, TYPE III; WT3