hereditary night blindness Gene Set

Dataset DISEASES Text-mining Gene-Disease Assocation Evidence Scores
Category disease or phenotype associations
Type disease
Description OMIM mapping confirmed by DO. [SN]. (Human Disease Ontology, DOID_8498)
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27 genes co-occuring with the disease hereditary night blindness in abstracts of biomedical publications from the DISEASES Text-mining Gene-Disease Assocation Evidence Scores dataset.

Symbol Name Standardized Value
GRK1 G protein-coupled receptor kinase 1 2.32723
RHO rhodopsin 2.24524
SAG S-antigen; retina and pineal gland (arrestin) 1.67457
CACNA1F calcium channel, voltage-dependent, L type, alpha 1F subunit 1.53348
RDH5 retinol dehydrogenase 5 (11-cis/9-cis) 1.43244
GRM6 glutamate receptor, metabotropic 6 1.36248
NYX nyctalopin 1.35594
CACNA2D3 calcium channel, voltage-dependent, alpha 2/delta subunit 3 1.20829
RGS11 regulator of G-protein signaling 11 1.17335
EGOT eosinophil granule ontogeny transcript (non-protein coding) 1.13459
NR2E3 nuclear receptor subfamily 2, group E, member 3 1.0669
RP2 retinitis pigmentosa 2 (X-linked recessive) 1.03577
GNAT1 guanine nucleotide binding protein (G protein), alpha transducing activity polypeptide 1 1.01512
ARRB1 arrestin, beta 1 0.947019
SLC1A7 solute carrier family 1 (glutamate transporter), member 7 0.928759
PADI2 peptidyl arginine deiminase, type II 0.832329
TRPM1 transient receptor potential cation channel, subfamily M, member 1 0.799923
VAMP2 vesicle-associated membrane protein 2 (synaptobrevin 2) 0.791311
ABCA4 ATP-binding cassette, sub-family A (ABC1), member 4 0.784345
CNGA3 cyclic nucleotide gated channel alpha 3 0.728952
PDE6B phosphodiesterase 6B, cGMP-specific, rod, beta 0.676308
SLC17A7 solute carrier family 17 (vesicular glutamate transporter), member 7 0.647348
GAB2 GRB2-associated binding protein 2 0.625319
RCVRN recoverin 0.583163
NDP Norrie disease (pseudoglioma) 0.578883
GK glycerol kinase 0.555956
MCM8 minichromosome maintenance complex component 8 0.40008