From Wikipedia, the free encyclopedia
Protein-coding gene in the species Homo sapiens
Blue-sensitive opsin is a
protein that in humans is encoded by the OPN1SW
gene .
[5]
[6]
[7]
See also
References
^
a
b
c
GRCh38: Ensembl release 89: ENSG00000128617 –
Ensembl , May 2017
^
a
b
c
GRCm38: Ensembl release 89: ENSMUSG00000058831 –
Ensembl , May 2017
^
"Human PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^
"Mouse PubMed Reference:" . National Center for Biotechnology Information, U.S. National Library of Medicine .
^ Nathans J, Thomas D, Hogness DS (Apr 1986). "Molecular genetics of human color vision: the genes encoding blue, green, and red pigments". Science . 232 (4747): 193–202.
Bibcode :
1986Sci...232..193N .
CiteSeerX
10.1.1.461.5915 .
doi :
10.1126/science.2937147 .
PMID
2937147 .
^ Fitzgibbon J, Appukuttan B, Gayther S, Wells D, Delhanty J, Hunt DM (Feb 1994). "Localisation of the human blue cone pigment gene to chromosome band 7q31.3-32". Hum Genet . 93 (1): 79–80.
doi :
10.1007/bf00218919 .
PMID
8270261 .
S2CID
43548690 .
^
"Entrez Gene: OPN1SW opsin 1 (cone pigments), short-wave-sensitive (color blindness, tritan)" .
Further reading
Applebury ML, Hargrave PA (1987). "Molecular biology of the visual pigments". Vision Res . 26 (12): 1881–95.
doi :
10.1016/0042-6989(86)90115-X .
PMID
3303660 .
S2CID
34038855 .
Swanson WH, Cohen JM (2003). "Color vision". Ophthalmology Clinics of North America . 16 (2): 179–203.
doi :
10.1016/S0896-1549(03)00004-X .
PMID
12809157 .
Weitz CJ, Went LN, Nathans J (1992).
"Human tritanopia associated with a third amino acid substitution in the blue-sensitive visual pigment" . Am. J. Hum. Genet . 51 (2): 444–6.
PMC
1682686 .
PMID
1386496 .
Weitz CJ, Miyake Y, Shinzato K, et al. (1992).
"Human tritanopia associated with two amino acid substitutions in the blue-sensitive opsin" . Am. J. Hum. Genet . 50 (3): 498–507.
PMC
1684278 .
PMID
1531728 .
Oprian DD, Asenjo AB, Lee N, Pelletier SL (1992). "Design, chemical synthesis, and expression of genes for the three human color vision pigments". Biochemistry . 30 (48): 11367–72.
doi :
10.1021/bi00112a002 .
PMID
1742276 .
Sarkar G, Sommer SS (1989). "Access to a messenger RNA sequence or its protein product is not limited by tissue or species specificity". Science . 244 (4902): 331–4.
Bibcode :
1989Sci...244..331S .
doi :
10.1126/science.2565599 .
PMID
2565599 .
Nathans J, Piantanida TP, Eddy RL, et al. (1986). "Molecular genetics of inherited variation in human color vision". Science . 232 (4747): 203–10.
Bibcode :
1986Sci...232..203N .
doi :
10.1126/science.3485310 .
PMID
3485310 .
Shimmin LC, Mai P, Li WH (1997). "Sequences and evolution of human and squirrel monkey blue opsin genes". J. Mol. Evol . 44 (4): 378–82.
Bibcode :
1997JMolE..44..378S .
doi :
10.1007/PL00006157 .
PMID
9089077 .
S2CID
6425474 .
Scherer SW, Cheung J, MacDonald JR, et al. (2003).
"Human Chromosome 7: DNA Sequence and Biology" . Science . 300 (5620): 767–72.
Bibcode :
2003Sci...300..767S .
doi :
10.1126/science.1083423 .
PMC
2882961 .
PMID
12690205 .
Gunther KL, Neitz J, Neitz M (2006). "A novel mutation in the short-wavelength-sensitive cone pigment gene associated with a tritan color vision defect". Vis. Neurosci . 23 (3–4): 403–9.
doi :
10.1017/S0952523806233169 .
PMID
16961973 .
S2CID
3748083 .