GEISHA - A Chicken Embryo Gene Expression Database
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VWFvon Willebrand disease, type 1VWF
VWFvon Willebrand disease, types 2A, 2B, 2M, and 2NVWF
VWFvon Willibrand disease, type 3VWF
MESP2Spondylocostal dysostosis, autosomal recessive 2MESP2
ZFAT1{Autoimmune thyroid disease, susceptibility to, 3}ZFAT
HYAL1Mucopolysaccharidosis type IXHYAL1
BARD1{Breast cancer, susceptibility to}BARD1
CRBNMental retardation, autosomal recessive 2CRBN
HCRTNarcolepsy 1HCRT
FRAS1Fraser syndromeFRAS1
VRK1Pontocerebellar hypoplasia type 1AVRK1
GAD1Cerebral palsy, spastic quadriplegic, 1GAD1
GRXCR1Deafness, autosomal recessive 25GRXCR1
FOXE3Anterior segment mesenchymal dysgenesisFOXE3
FOXE3Aphakia, congenital primaryFOXE3
MHC2TABare lymphocyte syndrome, type II, complementation group ACIITA
MHC2TA{Rheumatoid arthritis, susceptibility to}CIITA
NYXNight blindness, congenital stationary, type 1ANYX
KRT5Dowling-Degos diseaseKRT5
KRT5Epidermolysis bullosa simplex with migratory circinate erythemaKRT5
KRT5Epidermolysis bullosa simplex with mottled pigmentationKRT5
KRT5Epidermolysis bullosa simplex, Dowling-Meara typeKRT5
KRT5Epidermolysis bullosa simplex, Koebner typeKRT5
KRT5Epidermolysis bullosa simplex, Weber-Cockayne typeKRT5
EFEMP1Doyne honeycomb degeneration of retinaEFEMP1
PAX7Rhabdomyosarcoma 2, alveolarPAX7
ORC4Meier-Gorlin syndrome 2ORC4
ZEB2Mowat-Wilson syndromeZEB2
NEUROD1Maturity-onset diabetes of the young 6NEUROD1
NEUROD1{Diabetes mellitus, noninsulin-dependent}NEUROD1
AVPDiabetes insipidus, neurohypophysealAVP
ALDH7A1Epilepsy, pyridoxine-dependentALDH7A1
CSRP3Cardiomyopathy, dilated, 1MCSRP3
CSRP3Cardiomyopathy, familial hypertrophic, 12CSRP3
TAF15Chondrosarcoma, extraskeletal myxoidTAF15
GATA3Hypoparathyroidism, sensorineural deafness, and renal dysplasiaGATA3
LIPHHypotrichosis, localized, autosomal recessive 2LIPH
LIPHWoolly hair, autosomal recessive 2 with or without hypotrichosisLIPH
PRG4Camptodactyly-arthropathy-coxa vara-pericarditis syndromePRG4
PLAG1Adenomas, salivary gland pleomorphicPLAG1
MPICongenital disorder of glycosylation, type IbMPI
KCNE2Atrial fibrillation, familial, 4KCNE2
KCNE2Long QT syndrome-6KCNE2
TNFRSF11AOsteolysis, familial expansileTNFRSF11A
TNFRSF11AOsteopetrosis, autosomal recessive 7TNFRSF11A
TNFRSF11APaget disease of boneTNFRSF11A
SLC7A7Lysinuric protein intoleranceSLC7A7
GNASAcromegalyGNAS
GNASACTH-independent macronodular adrenal hyperplasiaGNAS
GNASMcCune-Albright syndromeGNAS
GNASOsseous heteroplasia, progressiveGNAS
GNASPseudohypoparathyroidism IaGNAS
GNASPseudohypoparathyroidism IbGNAS
GNASPseudohypoparathyroidism IcGNAS
GNASPseudopseudohypoparathyroidismGNAS
IFT80Asphyxiating thoracic dystrophy 2IFT80
JAK2Leukemia, acute myelogenousJAK2
JAK2Myelofibrosis, idiopathicJAK2
JAK2Polycythemia veraJAK2
JAK2Thrombocythemia 3JAK2
JAK2{Budd-Chiari syndrome}JAK2
CYP1B1Glaucoma 3A, primary congenitalCYP1C1
CYP1B1Glaucoma, primary open angle, adult-onsetCYP1C1
CYP1B1Glaucoma, primary open angle, juvenile-onsetCYP1C1
CYP1B1Peters anomalyCYP1C1
MAP3K146XY sex reversal 6MAP3K1
TREM2Nasu-Hakola diseaseTREM2
NIPAL4Ichthyosis, congenital, autosomal recessiveNIPAL4
AK2Reticular dysgenesisAK2
XIAPLymphoproliferative syndrome, X-linked, 2XIAP
GUCA1ACone dystrophy-3GUCA1A
GUCA1ACone-rod dystrophy 14GUCA1A
SCNN1BBronchiectasis with or without elevated sweat chloride 1SCNN1B
SCNN1BLiddle syndromeSCNN1B
SCNN1BPseudohypoaldosteronism, type ISCNN1B
SCNN1BDeafness, X-linked 1PRPS1
TRAPPC9Mental retardation, autosomal recessive 13TRAPPC9
HMBSPorphyria, acute intermittentHMBS
HMBSPorphyria, acute intermittent, nonerythroid variantHMBS
STARLipoid adrenal hyperplasiaSTAR
PNLIPPancreatic lipase deficiencyPNLIP
THBS2{Lumbar disc herniation, susceptibility to}THBS2
SH3PXD2BFrank-ter Haar syndromeSH3PXD2B
SAMHD1Aicardi-Goutieres syndrome 5SAMHD1
SAMHD1Chilblain lupus 2SAMHD1
HNF1ADiabetes mellitus, insulin-dependent, 20HNF1A
HNF1AHepatic adenoma, somaticHNF1A
HNF1AMODY, type IIIHNF1A
HNF1ARenal cell carcinomaHNF1A
HNF1A{Diabetes mellitus, insulin-dependent}HNF1A
HNF1A{Diabetes mellitus, noninsulin-dependent, 2}HNF1A
TEAD1Sveinsson choreoretinal atrophyTEAD1
NFKBIAEctodermal dysplasia, anhidrotic, with T-cell immunodeficiencyNFKBIA
RCBTB1{Alcohol dependence, susceptibility to}RCBTB1
MEF2A{Coronary artery disease, autosomal dominant, 1}MEF2A
PHGDHPhosphoglycerate dehydrogenase deficiencyPHGDH
PALLD{Pancreatic cancer, susceptibility to, 1}PALLD
NLGN4Mental retardation, X-linkedNLGN4X
NLGN4{Asperger syndrome susceptibility, X-linked 2}NLGN4X
NLGN4{Autism susceptibility, X-linked 2}NLGN4X
PDGFRBMyeloproliferative disorder with eosinophiliaPDGFRB
PHF6Borjeson-Forssman-Lehmann syndromePHF6
BTDBiotinidase deficiencyBTD
BMPERDiaphanospondylodysostosisBMPER
KRT75{Pseudofolliculitis barbae, susceptibility to}KRT75
STX11Hemophagocytic lymphohistiocytosis, familial, 4STX11
NR2E3Enhanced S-cone syndromeNR2E3
NR2E3Retinitis pigmentosa 37NR2E3
ANTXR2Fibromatosis, juvenile hyalineANTXR2
ANTXR2Hyalinosis, infantile systemicANTXR2
SPINK5AtopySPIK7
SPINK5Netherton syndromeSPIK7
OSMRAmyloidosis, primary localized cutaneous, 1OSMR
LRPPRCLeigh syndrome, French-Canadian typeLRPPRC
ANKRD26Thrombocytopenia 2ANKRD26
GALNT3Tumoral calcinosis, hyperphosphatemic, familialGALNT3
KNG1[High molecular weight kininogen deficiency]KNG1
KNG1[Kininogen deficiency]KNG1
TMIEDeafness, autosomal recessive 6TMIE
FADDInfections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malforamtionsFADD
SGCEDystonia-11, myoclonicSGCE
RAB23Carpenter syndromeRAB23
MMP9Metaphyseal anadysplasia 2MMP9
APCAdenomatous polyposis coliAPC
APCColorectal cancer, somaticAPC
APCDesmoid disease, hereditaryAPC
APCGastric cancer, somaticAPC
APCHepatoblastoma, somaticAPC
RGS9BradyopsiaRGS9
ROBO2Vesicoureteral reflux 2ROBO2
RPGRIP1LCOACH syndromeRPGRIP1L
RPGRIP1LJoubert syndrome 7RPGRIP1L
RPGRIP1LMeckel syndrome, type 5RPGRIP1L
EPB42Spherocytosis, hereditary, type 5EPB42
PLIN1Lipodystrophy, familial partial, type 4PLIN1
PRKAG2Cardiomyopathy, familial hypertrophic 6PRKAG2
PRKAG2Glycogen storage disease of heart, lethal congenitalPRKAG2
PRKAG2Wolff-Parkinson-White syndromePRKAG2
MLPHGriscelli syndrome, type 3MLPH
PIGAMultiple congenital anomalies-hypotonia-seizures syndrome 2PIGA
PIGAParoxysmal nocturnal hemoglobinuria, somaticPIGA
CTRC{Pancreatitis, chronic, susceptibility to}CTRC
EWSR1Ewing sarcomaEWSR1
EWSR1NeuroepitheliomaEWSR1
LFNGSpondylocostal dysostosis, autosomal recessive 3LFNG
GARSCharcot-Marie-Tooth disease, type 2DGARS
GARSNeuropathy, distal hereditary motor, type VGARS
CAPN10{Diabetes mellitus, noninsulin-dependent 1}CAPN10
RFXANKMHC class II deficiency, complementation group BRFXANK
AKAP9Long QT syndrome-11AKAP9
SLC17A5Salla diseaseSLC17A5
SLC17A5Sialic acid storage disorder, infantileSLC17A5
ALG8Congenital disorder of glycosylation, type IhALG8
ACAD8Isobutyryl-CoA dehydrogenase deficiencyACAD8
ATXN7Spinocerebellar ataxia 7ATXN7
BLMH{Alzheimer disease, susceptibility to}BLMH
C1QBC1q deficiencyC1QB
HMGA2Leiomyoma, uterine, somaticHMGA2
CAV1Lipodystrophy, congenital generalized, type 3CAV1
PDX1Lacticacidemia due to PDX1 deficiencyPDHX
PLAUQuebec platelet disorderPLAU
PLAU{Alzheimer disease, late-onset, susceptibility to}PLAU
COL6A3Bethlem myopathyCOL6A3
COL6A3Ullrich congenital muscular dystrophyCOL6A3
ERCC4Xeroderma pigmentosum, group FERCC4
ERCC4XFE progeroid syndromeERCC4
FHFumarase deficiencyFH
FHLeiomyomatosis and renal cell cancerFH
SLC52A3Fazio-Londe diseaseSLC52A3
HRASCostello syndromeHRAS
RRM2BMitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)RRM2B
RRM2BMitochondrial DNA depletion syndrome 8B (MNGIE type)RRM2B
SLC29A3Histiocytosis-lymphadenopathy plus syndromeSLC29A3
FMR1Fragile X syndromeFMR1
FMR1Fragile X tremor/ataxia syndromeFMR1
FMR1Premature ovarian failure 1FMR1
SELP{Atopy, susceptibility to}SELP
FSHBFollicle-stimulating hormone deficiency, isolatedFSHB
BRCA2Fanconi anemia, complementation group D1BRCA2
BRCA2Pancreatic cancerBRCA2
BRCA2Prostate cancerBRCA2
BRCA2Wilms tumorBRCA2
BRCA2{Breast cancer, male, susceptibility to}BRCA2
BRCA2{Breast-ovarian cancer, familial, 2}BRCA2
BRCA2{Glioblastoma 3}BRCA2
BRCA2{Medulloblastoma}BRCA2
IL10RAInflammatory bowel disease 28, early onset, autosomal recessiveIL10RA
CLN6Ceroid lipofuscinosis, neuronal, 6CLN6
CLN6Ceroid lipofuscinosis, neuronal, Kufs type, adult onsetCLN6
ITPR1Spinocerebellar ataxia 15ITPR1
COL17A1Epidermolysis bullosa, junctional, non-Herlitz typeCOL17A1
KCNJ2Atrial fibrillation, familial, 9KCNJ2
KCNJ2Long QT syndrome-7KCNJ2
KCNJ2Short QT syndrome-3KCNJ2
SCP2Leukoencephalopathy with dystonia and motor neuropathySCP2
CUBNMegaloblastic anemia-1, Finnish typeCUBN
CHRNA3{Lung cancer susceptibility 2}CHRNA3
CD36Platelet glycoprotein IV deficiencyCD36
CD36{Coronary heart disease, susceptibility to, 7}CD36
CD36{Malaria, cerebral, reduced risk of}CD36
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