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GenDaB Gene DataBase

Display options choose which data sources to show
Candidate Genes, Regions or Panels restrict your search to custom candidate genes
Gene symbols / Gene IDs
HGNC gene symbols, NCBI Gene IDs or ENSEMBL IDs,
which must be comma-separated.
* and % can be used as wildcards for gene symbols.
Regions from BED file
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Find all genes in these regions
Gene type
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Common Gene Panels
Genomics England PanelApp 
Cardiovascular disorders
Arteriopathies
Cardiac arrhythmia
Cardiomyopathy
Congenital heart disease
Connective tissue disorders and aortopathies
Lymphatic Disorders
Pulmonary heart disease
Ciliopathies
Congenital malformations caused by ciliopathies
Respiratory ciliopathies
Dermatological disorders
Atopy
Autoimmune skin disorders
Ectodermal dysplasias
Ichthyoses
Keratodermas
Skin adnexa disorders
Skin fragility disorders
Sun-exposure related conditions
Dysmorphic and congenital abnormality syndromes
Autophagy disorders
DNA repair disorders
Dysmorphic disorders
Fetal disorders
Kabuki
Limb disorders
RASopathies
Endocrine disorders
Adrenal disorders
Disorders of calcium homeostasis
Disorders of unusual phenotypes
Gonadal and sex development disorders
Growth hormone disorders
Hypothalamic and pituitary disorders
Obesity syndromes
Thyroid disorders
Gastroenterological disorders
Gastrointestinal disorders
Liver disease
Growth disorders
Beckwith-Wiedemann syndrome (BWS) and other congenital overgrowth disorders
Growth restriction
Haematological and immunological disorders
Haemostasis disorders
Haematological disorders
Anaemias and red cell disorders
Primary immunodeficiency disorders
Hearing and ear disorders
Deafness and congenital structural abnormalities
Non-syndromic hearing loss
Other hearing and ear disorders
Metabolic disorders
Lysosomal storage disorders
Mitochondrial
Peroxisomal disorders
Specific metabolic abnormalities
Urea Cycle disorders
Neurology and neurodevelopmental disorders
Cerebrovascular disorders
Channelopathies
Inherited Epilepsy Syndromes
Motor Disorders of the CNS
Motor and Sensory Disorders of the PNS
Neurodegenerative disorders
Neurodevelopmental disorders
Neuromuscular disorders
Parenchymal brain disorders
Sleep disorders
White matter disorders
Ophthalmological disorders
Anterior segment abnormalities
Ocular malformations
Ocular movement disorders
Posterior segment abnormalities
Renal and urinary tract disorders
Disorders of function
Structural renal and urinary tract disease
Syndromes with prominent renal abnormalities
Respiratory disorders
Interstitial lung disorders
Structural lung disorders
Vascular lung disorders
Rheumatological disorders
Connective tissues disorders
Multi-system inflammatory/autoimmune disorders
Skeletal disorders
Choanal anomalies
Craniosynostosis syndromes
Skeletal dysplasias
Tumour syndromes
Breast and endocrine
Childhood Tumours
GI tract
Muscle and nerve
Skin
Tumour syndromes
not grouped
Phenotypes enter HPO, OMIM, or Orphanet terms to describe your patient's phenotype
Search for these human phenotypes
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HPO
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Orphanet
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OMIM
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Search for these keywords (OMIM/Orphanet/GeneRIFs)
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Search for these broad mouse phenotypes
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Function enter GO, WikiPathways or Reactome terms
Search for function
To filter, search and select terms:
GeneOntology
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Reactome
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WikiPathways
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Interactions search for protein-protein interactions
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Interaction partners as NCBI gene IDs, ENSEMBL IDs or HGNC gene symbols
Expression restrict your search to genes expressed in specific organs or tissues
Developmental stage
Experimental method
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Tissue selection
Organs
 
Systems
 
Tissues
Cellular Localisation restrict your search to genes/proteins within cellular compartments

Select protein localisation here or use GO terms under 'Function'.









































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