GEISHA - A Chicken Embryo Gene Expression Database
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von Willebrand disease, type 1VWFVWF
von Willebrand disease, types 2A, 2B, 2M, and 2NVWFVWF
von Willibrand disease, type 3VWFVWF
Spondylocostal dysostosis, autosomal recessive 2MESP2MESP2
{Autoimmune thyroid disease, susceptibility to, 3}ZFAT1ZFAT
Mucopolysaccharidosis type IXHYAL1HYAL1
{Breast cancer, susceptibility to}BARD1BARD1
Mental retardation, autosomal recessive 2CRBNCRBN
Narcolepsy 1HCRTHCRT
Fraser syndromeFRAS1FRAS1
Pontocerebellar hypoplasia type 1AVRK1VRK1
Cerebral palsy, spastic quadriplegic, 1GAD1GAD1
Deafness, autosomal recessive 25GRXCR1GRXCR1
Anterior segment mesenchymal dysgenesisFOXE3FOXE3
Aphakia, congenital primaryFOXE3FOXE3
Bare lymphocyte syndrome, type II, complementation group AMHC2TACIITA
{Rheumatoid arthritis, susceptibility to}MHC2TACIITA
Night blindness, congenital stationary, type 1ANYXNYX
Dowling-Degos diseaseKRT5KRT5
Epidermolysis bullosa simplex with migratory circinate erythemaKRT5KRT5
Epidermolysis bullosa simplex with mottled pigmentationKRT5KRT5
Epidermolysis bullosa simplex, Dowling-Meara typeKRT5KRT5
Epidermolysis bullosa simplex, Koebner typeKRT5KRT5
Epidermolysis bullosa simplex, Weber-Cockayne typeKRT5KRT5
Doyne honeycomb degeneration of retinaEFEMP1EFEMP1
Rhabdomyosarcoma 2, alveolarPAX7PAX7
Meier-Gorlin syndrome 2ORC4ORC4
Mowat-Wilson syndromeZEB2ZEB2
Maturity-onset diabetes of the young 6NEUROD1NEUROD1
{Diabetes mellitus, noninsulin-dependent}NEUROD1NEUROD1
Diabetes insipidus, neurohypophysealAVPAVP
Epilepsy, pyridoxine-dependentALDH7A1ALDH7A1
Cardiomyopathy, dilated, 1MCSRP3CSRP3
Cardiomyopathy, familial hypertrophic, 12CSRP3CSRP3
Chondrosarcoma, extraskeletal myxoidTAF15TAF15
Hypoparathyroidism, sensorineural deafness, and renal dysplasiaGATA3GATA3
Hypotrichosis, localized, autosomal recessive 2LIPHLIPH
Woolly hair, autosomal recessive 2 with or without hypotrichosisLIPHLIPH
Camptodactyly-arthropathy-coxa vara-pericarditis syndromePRG4PRG4
Adenomas, salivary gland pleomorphicPLAG1PLAG1
Congenital disorder of glycosylation, type IbMPIMPI
Atrial fibrillation, familial, 4KCNE2KCNE2
Long QT syndrome-6KCNE2KCNE2
Osteolysis, familial expansileTNFRSF11ATNFRSF11A
Osteopetrosis, autosomal recessive 7TNFRSF11ATNFRSF11A
Paget disease of boneTNFRSF11ATNFRSF11A
Lysinuric protein intoleranceSLC7A7SLC7A7
AcromegalyGNASGNAS
ACTH-independent macronodular adrenal hyperplasiaGNASGNAS
McCune-Albright syndromeGNASGNAS
Osseous heteroplasia, progressiveGNASGNAS
Pseudohypoparathyroidism IaGNASGNAS
Pseudohypoparathyroidism IbGNASGNAS
Pseudohypoparathyroidism IcGNASGNAS
PseudopseudohypoparathyroidismGNASGNAS
Asphyxiating thoracic dystrophy 2IFT80IFT80
Leukemia, acute myelogenousJAK2JAK2
Myelofibrosis, idiopathicJAK2JAK2
Polycythemia veraJAK2JAK2
Thrombocythemia 3JAK2JAK2
{Budd-Chiari syndrome}JAK2JAK2
Glaucoma 3A, primary congenitalCYP1B1CYP1C1
Glaucoma, primary open angle, adult-onsetCYP1B1CYP1C1
Glaucoma, primary open angle, juvenile-onsetCYP1B1CYP1C1
Peters anomalyCYP1B1CYP1C1
46XY sex reversal 6MAP3K1MAP3K1
Nasu-Hakola diseaseTREM2TREM2
Ichthyosis, congenital, autosomal recessiveNIPAL4NIPAL4
Reticular dysgenesisAK2AK2
Lymphoproliferative syndrome, X-linked, 2XIAPXIAP
Cone dystrophy-3GUCA1AGUCA1A
Cone-rod dystrophy 14GUCA1AGUCA1A
Bronchiectasis with or without elevated sweat chloride 1SCNN1BSCNN1B
Liddle syndromeSCNN1BSCNN1B
Pseudohypoaldosteronism, type ISCNN1BSCNN1B
Deafness, X-linked 1SCNN1BPRPS1
Mental retardation, autosomal recessive 13TRAPPC9TRAPPC9
Porphyria, acute intermittentHMBSHMBS
Porphyria, acute intermittent, nonerythroid variantHMBSHMBS
Lipoid adrenal hyperplasiaSTARSTAR
Pancreatic lipase deficiencyPNLIPPNLIP
{Lumbar disc herniation, susceptibility to}THBS2THBS2
Frank-ter Haar syndromeSH3PXD2BSH3PXD2B
Aicardi-Goutieres syndrome 5SAMHD1SAMHD1
Chilblain lupus 2SAMHD1SAMHD1
Diabetes mellitus, insulin-dependent, 20HNF1AHNF1A
Hepatic adenoma, somaticHNF1AHNF1A
MODY, type IIIHNF1AHNF1A
Renal cell carcinomaHNF1AHNF1A
{Diabetes mellitus, insulin-dependent}HNF1AHNF1A
{Diabetes mellitus, noninsulin-dependent, 2}HNF1AHNF1A
Sveinsson choreoretinal atrophyTEAD1TEAD1
Ectodermal dysplasia, anhidrotic, with T-cell immunodeficiencyNFKBIANFKBIA
{Alcohol dependence, susceptibility to}RCBTB1RCBTB1
{Coronary artery disease, autosomal dominant, 1}MEF2AMEF2A
Phosphoglycerate dehydrogenase deficiencyPHGDHPHGDH
{Pancreatic cancer, susceptibility to, 1}PALLDPALLD
Mental retardation, X-linkedNLGN4NLGN4X
{Asperger syndrome susceptibility, X-linked 2}NLGN4NLGN4X
{Autism susceptibility, X-linked 2}NLGN4NLGN4X
Myeloproliferative disorder with eosinophiliaPDGFRBPDGFRB
Borjeson-Forssman-Lehmann syndromePHF6PHF6
Biotinidase deficiencyBTDBTD
DiaphanospondylodysostosisBMPERBMPER
{Pseudofolliculitis barbae, susceptibility to}KRT75KRT75
Hemophagocytic lymphohistiocytosis, familial, 4STX11STX11
Enhanced S-cone syndromeNR2E3NR2E3
Retinitis pigmentosa 37NR2E3NR2E3
Fibromatosis, juvenile hyalineANTXR2ANTXR2
Hyalinosis, infantile systemicANTXR2ANTXR2
AtopySPINK5SPIK7
Netherton syndromeSPINK5SPIK7
Amyloidosis, primary localized cutaneous, 1OSMROSMR
Leigh syndrome, French-Canadian typeLRPPRCLRPPRC
Thrombocytopenia 2ANKRD26ANKRD26
Tumoral calcinosis, hyperphosphatemic, familialGALNT3GALNT3
[High molecular weight kininogen deficiency]KNG1KNG1
[Kininogen deficiency]KNG1KNG1
Deafness, autosomal recessive 6TMIETMIE
Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovasuclar malforamtionsFADDFADD
Dystonia-11, myoclonicSGCESGCE
Carpenter syndromeRAB23RAB23
Metaphyseal anadysplasia 2MMP9MMP9
Adenomatous polyposis coliAPCAPC
Colorectal cancer, somaticAPCAPC
Desmoid disease, hereditaryAPCAPC
Gastric cancer, somaticAPCAPC
Hepatoblastoma, somaticAPCAPC
BradyopsiaRGS9RGS9
Vesicoureteral reflux 2ROBO2ROBO2
COACH syndromeRPGRIP1LRPGRIP1L
Joubert syndrome 7RPGRIP1LRPGRIP1L
Meckel syndrome, type 5RPGRIP1LRPGRIP1L
Spherocytosis, hereditary, type 5EPB42EPB42
Lipodystrophy, familial partial, type 4PLIN1PLIN1
Cardiomyopathy, familial hypertrophic 6PRKAG2PRKAG2
Glycogen storage disease of heart, lethal congenitalPRKAG2PRKAG2
Wolff-Parkinson-White syndromePRKAG2PRKAG2
Griscelli syndrome, type 3MLPHMLPH
Multiple congenital anomalies-hypotonia-seizures syndrome 2PIGAPIGA
Paroxysmal nocturnal hemoglobinuria, somaticPIGAPIGA
{Pancreatitis, chronic, susceptibility to}CTRCCTRC
Ewing sarcomaEWSR1EWSR1
NeuroepitheliomaEWSR1EWSR1
Spondylocostal dysostosis, autosomal recessive 3LFNGLFNG
Charcot-Marie-Tooth disease, type 2DGARSGARS
Neuropathy, distal hereditary motor, type VGARSGARS
{Diabetes mellitus, noninsulin-dependent 1}CAPN10CAPN10
MHC class II deficiency, complementation group BRFXANKRFXANK
Long QT syndrome-11AKAP9AKAP9
Salla diseaseSLC17A5SLC17A5
Sialic acid storage disorder, infantileSLC17A5SLC17A5
Congenital disorder of glycosylation, type IhALG8ALG8
Isobutyryl-CoA dehydrogenase deficiencyACAD8ACAD8
Spinocerebellar ataxia 7ATXN7ATXN7
{Alzheimer disease, susceptibility to}BLMHBLMH
C1q deficiencyC1QBC1QB
Leiomyoma, uterine, somaticHMGA2HMGA2
Lipodystrophy, congenital generalized, type 3CAV1CAV1
Lacticacidemia due to PDX1 deficiencyPDX1PDHX
Quebec platelet disorderPLAUPLAU
{Alzheimer disease, late-onset, susceptibility to}PLAUPLAU
Bethlem myopathyCOL6A3COL6A3
Ullrich congenital muscular dystrophyCOL6A3COL6A3
Xeroderma pigmentosum, group FERCC4ERCC4
XFE progeroid syndromeERCC4ERCC4
Fumarase deficiencyFHFH
Leiomyomatosis and renal cell cancerFHFH
Fazio-Londe diseaseSLC52A3SLC52A3
Costello syndromeHRASHRAS
Mitochondrial DNA depletion syndrome 8A (encephalomyopathic type with renal tubulopathy)RRM2BRRM2B
Mitochondrial DNA depletion syndrome 8B (MNGIE type)RRM2BRRM2B
Histiocytosis-lymphadenopathy plus syndromeSLC29A3SLC29A3
Fragile X syndromeFMR1FMR1
Fragile X tremor/ataxia syndromeFMR1FMR1
Premature ovarian failure 1FMR1FMR1
{Atopy, susceptibility to}SELPSELP
Follicle-stimulating hormone deficiency, isolatedFSHBFSHB
Fanconi anemia, complementation group D1BRCA2BRCA2
Pancreatic cancerBRCA2BRCA2
Prostate cancerBRCA2BRCA2
Wilms tumorBRCA2BRCA2
{Breast cancer, male, susceptibility to}BRCA2BRCA2
{Breast-ovarian cancer, familial, 2}BRCA2BRCA2
{Glioblastoma 3}BRCA2BRCA2
{Medulloblastoma}BRCA2BRCA2
Inflammatory bowel disease 28, early onset, autosomal recessiveIL10RAIL10RA
Ceroid lipofuscinosis, neuronal, 6CLN6CLN6
Ceroid lipofuscinosis, neuronal, Kufs type, adult onsetCLN6CLN6
Spinocerebellar ataxia 15ITPR1ITPR1
Epidermolysis bullosa, junctional, non-Herlitz typeCOL17A1COL17A1
Atrial fibrillation, familial, 9KCNJ2KCNJ2
Long QT syndrome-7KCNJ2KCNJ2
Short QT syndrome-3KCNJ2KCNJ2
Leukoencephalopathy with dystonia and motor neuropathySCP2SCP2
Megaloblastic anemia-1, Finnish typeCUBNCUBN
{Lung cancer susceptibility 2}CHRNA3CHRNA3
Platelet glycoprotein IV deficiencyCD36CD36
{Coronary heart disease, susceptibility to, 7}CD36CD36
{Malaria, cerebral, reduced risk of}CD36CD36
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