Genes, Locations and Genetic Disorders on Chromosome 11

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
AA GDB:56898411p15-11p15 ATROPHIA AREATA; AA
ABCC8 GDB:59137011p15.1-11p15.1 SULFONYLUREA RECEPTOR; SUR
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY
ACAT1 GDB:12686111q22.3-11q23.1 ALPHA-METHYLACETOACETICACIDURIA
AMPD3 GDB:13601311p15-11p15 11pter-11p13 ADENOSINE MONOPHOSPHATE DEAMINASE-3; AMPD3
ANC GDB:995448411q22-11qter CANAL CARCINOMA
APOA1 GDB:11968411q23.3-11q23.3 APOLIPOPROTEIN A-I OF HIGH DENSITY LIPOPROTEIN; APOA1
APOA4 GDB:11900011q23-11q23 11q23-11qter APOLIPOPROTEIN A-IV; APOA4
APOC3 GDB:11900111q23.1-11q23.2 11q23.2-11q23.3 APOLIPOPROTEIN C-III; APOC3
ATM GDB:59336411q22-11q23 11q22.3-11q22.3 ATAXIA-TELANGIECTASIA; AT
BCL1 GDB:11972411q13.3-11q13.3 LEUKEMIA, CHRONIC LYMPHATIC; CLL
BWS GDB:12056711p15.5-11p15.5 BECKWITH-WIEDEMANN SYNDROME; BWS
C1NH GDB:11904111q12.1-11q13.1 ANGIONEUROTIC EDEMA, HEREDITARY; HANE
CALCA GDB:12057111p15.2-11p15.1 CALCITONIN/CALCITONIN-RELATED POLYPEPTIDE, ALPHA; CALCA
CAT GDB:11904911p13-11p13 CATALASE; CAT
CCND1 GDB:12822211q13.1-11q13.1 11q13.3-11q13.3 CYCLIN D1; CCND1
CD3E GDB:11976411q23-11q23 11q23.3-11q23.3 CD3E ANTIGEN, EPSILON POLYPEPTIDE; CD3E
CD3G GDB:11976511q23-11q23 11q23.3-11q23.3 T3 T-CELL ANTIGEN, GAMMA CHAIN; T3G; CD3G
CD59 GDB:11976911p13-11p13 CD59 ANTIGEN P18-20; CD59
HUMAN LEUKOCYTE ANTIGEN MIC11; MIC11
CDKN1C GDB:59329611p15.5-11p15.5 CYCLIN-DEPENDENT KINASE INHIBITOR 1C; CDKN1C
CLN2 GDB:12522811p15-11p15 CEROID-LIPOFUSCINOSIS, NEURONAL 2, LATE INFANTILE TYPE; CLN2
CNTF GDB:12591911q12-11q12 11q12.2-11q12.2 CILIARY NEUROTROPHIC FACTOR; CNTF
CPT1A GDB:59764211q-11q 11q13.1-11q13.5 HYPOGLYCEMIA, HYPOKETOTIC, WITH DEFICIENCY OF CARNITINE PALMITOYLTRANSFERASE
CARNITINE PALMITOYLTRANSFERASE I, LIVER; CPT1A
DDB1 GDB:59501411q12-11q13 DNA DAMAGE-BINDING PROTEIN; DDB1
DDB2 GDB:59501511p12-11p11 DNA DAMAGE-BINDING PROTEIN-2; DDB2
DHCR7 GDB:983530211q13.2-11q13.5 SMITH-LEMLI-OPITZ SYNDROME
DRD4 GDB:12778211p15.5-11p15.5 DOPAMINE RECEPTOR D4; DRD4
ECB2 GDB:995895511q23-11q23 POLYCYTHEMIA, BENIGN FAMILIAL
EVR1 GDB:13402911q13-11q13 EXUDATIVE VITREORETINOPATHY, FAMILIAL; EVR
EXT2 GDB:34492111p12-11p11 11p12-11q12 EXOSTOSES, MULTIPLE, TYPE II; EXT2
CHONDROSARCOMA
F2 GDB:11989411p11-11q12 COAGULATION FACTOR II; F2
FSHB GDB:11995511p13-11p13 FOLLICLE-STIMULATING HORMONE, BETA POLYPEPTIDE; FSHB
FTH1 GDB:12061711q13-11q13 FERRITIN HEAVY CHAIN 1; FTH1
GIF GDB:11880011q12-11q13 PERNICIOUS ANEMIA, CONGENITAL, DUE TO DEFECT OF INTRINSIC FACTOR
GSD1B GDB:983761911q23-11q23 GLYCOGEN STORAGE DISEASE Ib
GSD1C GDB:983763711q-11q STORAGE DISEASE Ic
HBB GDB:11929711p15.4-11p15.4 HEMOGLOBIN--BETA LOCUS; HBB
HBBP1 GDB:12003511p15.5-11p15.5 HEMOGLOBIN--BETA LOCUS; HBB
HBD GDB:11929811p15.5-11p15.5 HEMOGLOBIN--DELTA LOCUS; HBD
HBE1 GDB:11929911p15.5-11p15.5 HEMOGLOBIN--EPSILON LOCUS; HBE1
HBG1 GDB:11930011p15.5-11p15.5 HEMOGLOBIN, GAMMA A; HBG1
HBG2 GDB:11930111p15.5-11p15.5 HEMOGLOBIN, GAMMA G; HBG2
HMBS GDB:12052811q23.3-11q23.3 11q22.3-11q22.3 PORPHYRIA, ACUTE INTERMITTENT; AIP
HND GDB:995447811q13-11q13 HARTNUP DISORDER
HOMG2 GDB:995648411q23-11q23 MAGNESIUM WASTING, RENAL
HRAS GDB:12068411p15.5-11p15.5 V-HA-RAS HARVEY RAT SARCOMA VIRAL ONCOGENE HOMOLOG; HRAS
HVBS1 GDB:12006911p14-11p13 CANCER, HEPATOCELLULAR
IDDM2 GDB:12853011p15.5-11p15.5 DIABETES MELLITUS, INSULIN-DEPENDENT, 2
DIABETES MELLITUS, JUVENILE-ONSET INSULIN-DEPENDENT; IDDM
IGER GDB:11969611q12-11q13 IgE RESPONSIVENESS, ATOPIC; IGER
INS GDB:11934911p15.5-11p15.5 INSULIN; INS
JBS GDB:12011111q24.1-11q24.1 JACOBSEN SYNDROME; JBS
KCNJ11 GDB:700989311p15.1-11p15.1 POTASSIUM CHANNEL, INWARDLY-RECTIFYING, SUBFAMILY J, MEMBER 11; KCNJ11
PERSISTENT HYPERINSULINEMIC HYPOGLYCEMIA OF INFANCY
KCNJ1 GDB:20420611q24-11q24 POTASSIUM CHANNEL, INWARDLY-RECTIFYING, SUBFAMILY J, MEMBER 1; KCNJ1
KCNQ1 GDB:74124411p15.5-11p15.5 LONG QT SYNDROME, TYPE 1; LQT1
LDHA GDB:12014111p15.1-11p15.1 11p15.4-11p15.4 LACTATE DEHYDROGENASE-A; LDHA
MEN1 GDB:12017311q13-11q13 MULTIPLE ENDOCRINE NEOPLASIA, TYPE 1; MEN1
MLL GDB:12881911q23-11q23 11q23.3-11q23.3 MYELOID/LYMPHOID OR MIXED-LINEAGE LEUKEMIA; MLL
MTACR1 GDB:12574311p15.5-11p15.5 MULTIPLE TUMOR ASSOCIATED CHROMOSOME REGION 1; MTACR1
MYBPC3 GDB:57961511p11.2-11p11.2 CARDIOMYOPATHY, FAMILIAL HYPERTROPHIC, 4; CMH4
MYOSIN-BINDING PROTEIN C, CARDIAC; MYBPC3
MYO7A GDB:13254311q13.5-11q13.5 MYOSIN VIIA; MYO7A
DEAFNESS, NEUROSENSORY, AUTOSOMAL RECESSIVE, 2; DFNB2
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 11; DFNA11
OPPG GDB:378943811q12-11q13 OSTEOPOROSIS-PSEUDOGLIOMA SYNDROME; OPPG
OPTB1 GDB:995447411q12-11q13 OSTEOPETROSIS, AUTOSOMAL RECESSIVE
PALS GDB:918555211q14-11q14 KERATOSIS PALMOPLANTARIS WITH PERIODONTOPATHIA
PAX6 GDB:11899711p13-11p13 PAIRED BOX HOMEOTIC GENE 6; PAX6
PC GDB:11947211q11-11q13.1 11q13-11q13 11q13.4-11q13.5 PYRUVATE CARBOXYLASE DEFICIENCY
PDX1 GDB:983663411p13-11p13 PYRUVATE DEHYDROGENASE COMPLEX, COMPONENT X
PFM1 GDB:995447011p12-11p11.12 PARIETAL FORAMINA, SYMMETRIC; PFM
PGL1 GDB:13245611q22-11q23 PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 1; PGL1
PGL2 GDB:51117711q13.1-11q13.1 PARAGANGLIOMAS, FAMILIAL NONCHROMAFFIN, 2; PGL2
PGR GDB:11949311q22.1-11q22.3 11q22.2-11q22.2 PROGESTERONE RESISTANCE
PORC GDB:12861011q23.1-11q23.1 PORPHYRIA, CHESTER TYPE; PORC
PTH GDB:11952211p15.2-11p15.1 PARATHYROID HORMONE; PTH
PTS GDB:11885611q22.3-11q23.3 6-@PYRUVOYLTETRAHYDROPTERIN SYNTHASE; PTS
PYGM GDB:12032911q13.1-11q13.1 GLYCOGEN STORAGE DISEASE V
RAG1 GDB:12033411p13-11p13 RECOMBINATION ACTIVATING GENE-1; RAG1
RAG2 GDB:12518611p13-11p13 RECOMBINATION ACTIVATING GENE-2; RAG2
ROM1 GDB:12035011q13-11q13 ROD OUTER SEGMENT PROTEIN-1; ROM1
SAA1 GDB:12036411p15.1-11p14 11p15.1-11p15.1 SERUM AMYLOID A1; SAA1
SCA5 GDB:37821911p12-11q12 11q13.1-11q13.3 SPINOCEREBELLAR ATAXIA 5; SCA5
SCZD2 GDB:11887411q14-11q21 DISORDER-2; SCZD2
SMPD1 GDB:12814411p15.3-11p15.3 11p15.4-11p15.4 NIEMANN-PICK DISEASE
TCL2 GDB:995446811p13-11p13 LEUKEMIA, ACUTE T-CELL; ATL
TECTA GDB:683771811q22-11q24 11q23-11q24 11pter-11qter DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 8; DFNA8
DEAFNESS, AUTOSOMAL DOMINANT NONSYNDROMIC SENSORINEURAL, 12; DFNA12
TH GDB:11961211p15.5-11p15.5 TYROSINE HYDROXYLASE; TH
TSG101 GDB:131341411p15-11p15 11p15.2-11p15.1 TUMOR SUSCEPTIBILITY GENE 101; TSG101
TYR GDB:12047611q21-11q21 ALBINISM I
USH1C GDB:13254411p14-11p14 11p15.2-11p14 11p15.1-11p15.1 USHER SYNDROME, TYPE IC; USH1C
VMD2 GDB:13379511q13-11q13 VITELLIFORM MACULAR DYSTROPHY; VMD2
VRNI GDB:13566211q13-11q13 VITREORETINOPATHY, NEOVASCULAR INFLAMMATORY; VRNI
WT1 GDB:12049611p13-11p13 FRASIER SYNDROME
WILMS TUMOR; WT1
WT2 GDB:11888611p15-11p15 11p15.5-11p15.5 MULTIPLE TUMOR ASSOCIATED CHROMOSOME REGION 1; MTACR1