Homo Sapiens
RHO - Rhodopsin
Alias:
RP4
OPN2
CSNBAD1
The protein encoded by this gene is found in rod cells in the back of the eye and is essential for vision in low-light conditions. The encoded protein binds to 11-cis retinal and is activated when light hits the retinal molecule. Defects in this gene are a cause of congenital stationary night blindness. [provided by RefSeq, Aug 2017]
Basic Information
NCBI
Transcripts
Exons
Length
MW (kDa)
Mutations
Related Diseases
Related Models
Reference
RHO Genetics information (+)
GRCh38
Chr : -
Sequence Homology
Selected Gene:
Human：RHO
Disease & Mutation
#
Disease
Anatomical category
Score
Count
Transcripts & Proteins
Table View
Tile View
#
Transcript
Length(nt)
Exon count
CDS(bp)
Protein
Length(aa)
* This data comes from NCBI.
Gene Expression
Tissue-specific RNA expression
Organ
Expression
Alphabetical
Cell-specific RNA expression
Organ
Expression
Alphabetical
Protein Interaction
Acting
Regulation
Detail
Mechanism
Target
Residues
Reference
Score
Related Models
Type
Name
MGI
Strain of Origin
Publications
Drugs
Name
CAS Number
Status
Phase
Link
References
Title
PMID
Journal
Year
IF
