nephritis Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0000123
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Genes

24 genes associated with the nephritis phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
ALMS1 Alstrom syndrome protein 1
C1QA complement component 1, q subcomponent, A chain
C1QB complement component 1, q subcomponent, B chain
C1QC complement component 1, q subcomponent, C chain
C1R complement component 1, r subcomponent
C3 complement component 3
C4A complement component 4A (Rodgers blood group)
CASP10 caspase 10, apoptosis-related cysteine peptidase
CD151 CD151 molecule (Raph blood group)
CFH complement factor H
CFHR5 complement factor H-related 5
CFI complement factor I
COL4A3 collagen, type IV, alpha 3 (Goodpasture antigen)
COL4A4 collagen, type IV, alpha 4
COL4A5 collagen, type IV, alpha 5
DNASE1L3 deoxyribonuclease I-like 3
KCTD1 potassium channel tetramerization domain containing 1
LMX1B LIM homeobox transcription factor 1, beta
MYH9 myosin, heavy chain 9, non-muscle
PGM3 phosphoglucomutase 3
PLG plasminogen
PRKCD protein kinase C, delta
TREX1 three prime repair exonuclease 1
XDH xanthine dehydrogenase