GenTIGSA Gene Database on Rare Genetic Disorders
  Beta Version
Congenital Stationary Night Blindness  
Disease Aliases (8)

Congenital essential nyctalopia

Congenital stationary night blindness with myopia

Hemeralopia-myopia

Myopia-night blindness

X-linked csnb

X-linked congenital stationary night blindness

Xlcsnb

Congenital stationary night blindness, x-linked

Associated Genes (15)
 

NCBI-RefSeq:  GNB3   (G protein subunit beta 3)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  GRM6   (Glutamate metabotropic receptor 6)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  LRIT3   (Leucine rich repeat, Ig-like and transmembrane domains 3)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  TRPM1   (Transient receptor potential cation channel subfamily M member 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  NYX   (Nyctalopin)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  CACNA2D4   (Calcium voltage-gated channel auxiliary subunit alpha2delta 4)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  CACNA1F   (Calcium voltage-gated channel subunit alpha1 F)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  CABP4   (Calcium binding protein 4)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  PDE6B   (Phosphodiesterase 6B)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  SAG   (S-antigen visual arrestin)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  GRK1   (G protein-coupled receptor kinase 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  RHO   (Rhodopsin)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  GPR179   (G protein-coupled receptor 179)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  GNAT1   (G protein subunit alpha transducin 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 

NCBI-RefSeq:  SLC24A1   (Solute carrier family 24 member 1)

External Links:  gnomAD browser   Ensembl   GeneCards

 


Cross-references of Congenital stationary night blindness OMIM GARD Orphanet NCBI-GTR NCBI-MedGen MalaCards      MeSH Annotations