Genes, Locations and Genetic Disorders on Chromosome Unknown_or_Multiple_Locations

Last Updated: Sun Aug 6 22:00:02 EDT 2000
GeneGDB AccessionIDLocationOMIM Link
ABAT GDB:581658 GAMMA-AMINOBUTYRATE TRANSAMINASE
AEZ GDB:128360 ACRODERMATITIS ENTEROPATHICA, ZINC-DEFICIENCY TYPE; AEZ
AFA GDB:265277 FILIFORME ADNATUM AND CLEFT PALATE
ASAH GDB:6837715 FARBER LIPOGRANULOMATOSIS
ASD1 GDB:6276019 ATRIAL SEPTAL DEFECT; ASD
ASMT GDB:136259 ACETYLSEROTONIN METHYLTRANSFERASE; ASMT
ACETYLSEROTONIN METHYLTRANSFERASE, Y-CHROMOSOMAL; ASMTY; HIOMTY
BCH GDB:118758 CHOREA, HEREDITARY BENIGN; BCH
BDB1 GDB:9864171 BRACHYDACTYLY, TYPE B; BDB
BSCL GDB:9957720 SEIP SYNDROME
BZS GDB:265278 MACROCEPHALY, MULTIPLE LIPOMAS AND HEMANGIOMATA
CCAT GDB:118738 CATARACT, CONGENITAL OR JUVENILE
CHED2 GDB:9957389 CORNEAL DYSTROPHY, CONGENITAL HEREDITARY
CLA1 GDB:119781 CEREBELLOPARENCHYMAL DISORDER III
CLA3 GDB:128453 CEREBELLOPARENCHYMAL DISORDER I; CPD I
CLN4 GDB:125229 CEROID-LIPOFUSCINOSIS, NEURONAL 4; CLN4
CPO GDB:119070 COPROPORPHYRIA
CSF2RA GDB:118777 COLONY STIMULATING FACTOR 2 RECEPTOR, ALPHA; CSF2RA
GRANULOCYTE-MACROPHAGE COLONY-STIMULATING FACTOR RECEPTOR, ALPHA SUBUNIT,
CTS1 GDB:118779 CARPAL TUNNEL SYNDROME; CTS; CTS1
DF GDB:132645 FACTOR D
DIH1 GDB:439243 DIAPHRAGMATIC
DWS GDB:128371 SYNDROME; DWS
DYT2 GDB:118788 DYSTONIA MUSCULORUM DEFORMANS 2; DYT2
DYT4 GDB:433751 DYSTONIA MUSCULORUM DEFORMANS 4; DYT4
EBR3 GDB:118739 EPIDERMOLYSIS BULLOSA DYSTROPHICA NEUROTROPHICA
ECT GDB:128640 CENTRALOPATHIC EPILEPSY
ED# GDB:6928857 ECTODERMAL DYSPLASIA, ANHIDROTIC
ED4 GDB:9837373 DYSPLASIA, MARGARITA TYPE
EEF1A1L14 GDB:1327185 PROSTATIC CARCINOMA ONCOGENE PTI-1
EPX GDB:377700 EOSINOPHIL PEROXIDASE; EPX
EYCL2 GDB:4642815 EYE COLOR-3; EYCL3
FA1 GDB:118795 FANCONI ANEMIA, COMPLEMENTATION GROUP A; FACA
FANCE GDB:1220236 FANCONI ANEMIA, COMPLEMENTATION GROUP E; FACE
GCSH GDB:126842 HYPERGLYCINEMIA, ISOLATED NONKETOTIC, TYPE III; NKH3
GCSL GDB:132139 ISOLATED NONKETOTIC, TYPE IV; NKH4
GIP GDB:119985 GASTRIC INHIBITORY POLYPEPTIDE; GIP
GTS GDB:118807 GILLES DE LA TOURETTE SYNDROME; GTS
HHG GDB:118740 HYPERGONADOTROPIC HYPOGONADISM; HHG
HMI GDB:265275 OF ITO; HMI
HOAC GDB:118812 DEAFNESS, CONGENITAL, AUTOSOMAL RECESSIVE
HOKPP2 GDB:595535 HYPOKALEMIC PERIODIC PARALYSIS, TYPE II; HOKPP2
HSD3B3 GDB:676973 GIANT CELL HEPATITIS, NEONATAL
HTC1 GDB:265286 HYPERTRICHOSIS UNIVERSALIS CONGENITA, AMBRAS TYPE; HTC1
HV1S GDB:9955009 HERPES VIRUS SENSITIVITY; HV1S
ICR1 GDB:127785 LAMELLAR, AUTOSOMAL DOMINANT FORM
ICR5 GDB:127789 ICHTHYOSIS CONGENITA, HARLEQUIN FETUS TYPE
IDDM1 GDB:9953173 DIABETES MELLITUS, JUVENILE-ONSET INSULIN-DEPENDENT; IDDM
IL3RA GDB:128985 INTERLEUKIN-3 RECEPTOR, ALPHA; IL3RA
INTERLEUKIN-3 RECEPTOR, Y-CHROMOSOMAL; IL3RA
KAL2 GDB:265288 KALLMANN SYNDROME 2; KAL2
KMS GDB:118827 SYNDROME; KMS
KRT18 GDB:120127 KERATIN 18; KRT18
KSS GDB:9957718 KEARNS-SAYRE SYNDROME; KSS
LCAT GDB:119359 FISH-EYE DISEASE; FED
LECITHIN:CHOLESTEROL ACYLTRANSFERASE DEFICIENCY
LIMM GDB:9958161 MYOPATHY, MITOCHONDRIAL, LETHAL INFANTILE; LIMM
MANBB GDB:125262 MANNOSIDOSIS, BETA; MANB1
MCPH2 GDB:9863035 MICROCEPHALY; MCT
MEB GDB:599557 DISEASE
MELAS GDB:9955855 MELAS SYNDROME
MERRF GDB:9864723 MERRF SYNDROME
MIC2 GDB:120184 SURFACE ANTIGEN MIC2; MIC2; CD99
MIC2 SURFACE ANTIGEN, Y-CHROMOSOMAL; MIC2Y
MNGIE GDB:9835128 MYONEUROGASTROINTESTINAL ENCEPHALOPATHY SYNDROME
MPFD GDB:439372 CONGENITAL, WITH FIBER-TYPE DISPROPORTION
MS GDB:229116 SCLEROSIS; MS
MSS GDB:118743 MARINESCO-SJOGREN SYNDROME; MSS
MTATP6 GDB:118897 ATP SYNTHASE 6; MTATP6
MTCO1 GDB:118900 COMPLEX IV, CYTOCHROME c OXIDASE SUBUNIT I; MTCO1; COI
MTCO3 GDB:118902 CYTOCHROME c OXIDASE III; MTCO3
MTCYB GDB:118906 COMPLEX III, CYTOCHROME b SUBUNIT
MTND1 GDB:118911 COMPLEX I, SUBUNIT ND1; MTND1
MTND2 GDB:118912 COMPLEX I, SUBUNIT ND2; MTND2
MTND4 GDB:118914 COMPLEX I, SUBUNIT ND4; MTND4
MTND5 GDB:118916 COMPLEX I, SUBUNIT ND5; MTND5
MTND6 GDB:118917 COMPLEX I, SUBUNIT ND6; MTND6
MTTE GDB:118926 TRANSFER RNA, MITOCHONDRIAL, GLUTAMIC ACID; MTTE
MTTG GDB:118933 TRANSFER RNA, MITOCHONDRIAL, GLYCINE; MTTG
MTTI GDB:118935 TRANSFER RNA, MITOCHONDRIAL, ISOLEUCINE; MTTI
MTTK GDB:118936 MERRF SYNDROME
TRANSFER RNA, MITOCHONDRIAL, LYSINE; MTTK
MTTL1 GDB:118937 MERRF SYNDROME
TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 1; MTTL1
MTTL2 GDB:118938 TRANSFER RNA, MITOCHONDRIAL, LEUCINE, 2; MTTL2
MTTS1 GDB:118944 TRANSFER RNA, MITOCHONDRIAL, SERINE, 1; MTTS1
NODAL GDB:9848762 NODAL, MOUSE, HOMOLOG OF
OCD1 GDB:118846 DISORDER-1; OCD1
OPD2 GDB:131394 SYNDROME
PCK2 GDB:137198 PHOSPHOENOLPYRUVATE CARBOXYKINASE 2, MITOCHONDRIAL; PCK2
PCLD GDB:433949 POLYCYSTIC LIVER DISEASE; PLD
PEX12 GDB:6155804 PEROXIN-12; PEX12
PFKM GDB:120277 GLYCOGEN STORAGE DISEASE VII
PKD3 GDB:127866 KIDNEY DISEASE 3, AUTOSOMAL DOMINANT; PKD3
PPARA GDB:202877 PEROXISOME PROLIFERATOR ACTIVATED RECEPTOR, ALPHA; PPARA
PPP1R3 GDB:136797 PROTEIN PHOSPHATASE 1, REGULATORY (INHIBITOR) SUBUNIT 3; PPP1R3
PRCA1 GDB:342066 PROSTATE CANCER; PRCA1
PRO1 GDB:128585
PROP1 GDB:9834318 PROPHET OF PIT1, MOUSE, HOMOLOG OF; PROP1
RBS GDB:118862 ROBERTS SYNDROME; RBS
RFXAP GDB:9475355 REGULATORY FACTOR X-ASSOCIATED PROTEIN; RFXAP
SLC25A6 GDB:125184 ADENINE NUCLEOTIDE TRANSLOCATOR 3; ANT3
ADENINE NUCLEOTIDE TRANSLOCATOR 3, Y-CHROMOSOMAL; ANT3Y
SPG5B GDB:250333 SPASTIC PARAPLEGIA-5B, AUTOSOMAL RECESSIVE; SPG5B
STO GDB:439375 CEREBRAL GIGANTISM
SUOX GDB:5584405 SULFOCYSTEINURIA
TC21 GDB:5573831 ONCOGENE TC21
TREH GDB:9958953 TREHALASE
TST GDB:134043 RHODANESE; RDS