Browse Genes Associated with Rare Diseases
The table below displays a list of all genes contained within RARe-SOURCE™, which are associated with rare diseases. The table lists rare diseases linked to the gene, links to related features within RARe-SOURCE™ and links to external data sources. Clicking on the gene name, displays its genomic location, disease associations obtained from other data sources, and most recent publications on the gene from PubMed. Clicking on the associated rare disease lands on the ‘Rare Disease Information’ page with specific details on the disease.
AFF2 AF4/FMR2 family member 2 |
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ARFGEF2 ADP ribosylation factor guanine nucleotide exchange factor 2 |
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CSF2RA colony stimulating factor 2 receptor subunit alpha |
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CSF2RB colony stimulating factor 2 receptor subunit beta |
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CYP4F22 cytochrome P450 family 4 subfamily F member 22 |
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DNAAF2 dynein axonemal assembly factor 2 |
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DPF2 double PHD fingers 2 |
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EEF2 eukaryotic translation elongation factor 2 |
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EIF2AK2 eukaryotic translation initiation factor 2 alpha kinase 2 |
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EIF2AK3 eukaryotic translation initiation factor 2 alpha kinase 3 |
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EIF2AK4 eukaryotic translation initiation factor 2 alpha kinase 4 |
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EIF2S3 eukaryotic translation initiation factor 2 subunit gamma |
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F2 coagulation factor II, thrombin |
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FGF23 fibroblast growth factor 23 |
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GDF2 growth differentiation factor 2 |
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GINGF2 Fibromatosis, gingival, 2 |
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GTF2E2 general transcription factor IIE subunit 2 |
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GTF2H5 general transcription factor IIH subunit 5 |
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GTF2I general transcription factor IIi |
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GTF2IRD1 GTF2I repeat domain containing 1 |
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GTF2IRD2 GTF2I repeat domain containing 2 |
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H19-ICR H19-IGF2-imprinting control region |
Variants (0)
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IGF2 insulin like growth factor 2 |
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INF2 inverted formin, FH2 and WH2 domain containing |
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IRF2BP2 interferon regulatory factor 2 binding protein 2 |
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