Human
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
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CAS Number
Status
Phase
Link
References
Title
PMID
Journal
Year
IF
