Human beings have 23 pairs of chromosomes. Out of these 23 pairs 22 are autosomal chromosomes which are equal in both sexes and encode body functions. Only one pair consists of two sex-chromosomes which are different for men and women. The 22 pairs of equal chromosomes are numbered from 1 through to 22. The sex-chromosomes are labeled with X and Y, whereas women carry the combination XX and men the combination XY. This all sums up in a total of 46 chromosomes which make the human genome.
Color blindness was actually the trigger to start mapping the human genome. It all began in 1911, when red-green color blindness was assigned to the X chromosome. This was based upon the observation that color blindness is passed from mothers to their sons. Thereby the women are usually not affected because of the normal copy, the second X chromosome. Men in contrary can not oversteer the defective chromosome, because they are carrying just one X chromosome.
The project to decipher the whole human genome is these days much more advanced. Scientists are working eagerly to encode the whole approximately 30’000 genes in the human genome.
If we have a closer look at the chromosomes which are involved into color blindness, we should distinguish between the different types of color blindness because they are encoded at different places in the genome.
- Red-green color blindness
This term combines four different types of color blindness. Protanomaly and protanopia are caused by defective or even missing L-cones (long-wavelengths). In opposite defective or missing M-cones (medium-wavelengths) are the source of deuteranomaly or deuteranopia. The genes encoding the L- and M-cone photopigments are located side by side on the X chromosome. Because of the genes are highly homologous and adjacent to one another, recombinations between them is common and can lead to anomalous pigments. - Blue cone monochromacy
As this type of monochromacy is caused by a complete absence of L- and M-cones, blue cone monochromacy is encoded at the same place as red-green color blindness on the X chromosome. - Blue-yellow color blindness
Tritanomaly and tritanopia which are commonly referred to as blue-yellow color blindness are caused by defective or missing S-cones (short-wavelength). These photopigments are encoded in genes which reside on chromosome 7, an autosomal chromosome. This is why blue-yellow color blindness occures at the same rate on both sexes. - Rod monochromacy
The total loss of color vision is called rod monochromacy or complete achromatopsia. In this case the retina does not have any cone cells at all. It is known to be an autosomal recessive disease and can be provoked by different circumstances. Recent studies show that it can be encoded on chromosome 2 as well as on chromosome 8. Earlier studies assigned chromosome 14 to rod monochromacy but this could not be reconstructed.
The genes encoding L-, M- and S-cone photopigments are very well understood and determined whereas the source of rod monochromacy is a topic which still needs further research. Supposably different circumstances can cause rod monochromacy.
| Type | Chromosome |
| Deuteranomaly | X Chromosome |
| Deuteranopia | X Chromosome |
| Protanomaly | X Chromosome |
| Protanopia | X Chromosome |
| Tritanomaly | Chromosome 7 |
| Tritanopia | Chromosome 7 |
| Blue Cone Monochromacy | X Chromosome |
| Rod Monochromacy | Chromosome 2/8 |
The table on the left hand side shows on a glance the different types of color blindness and their related chromosomes. We have at least 4 different chromosomes out of the 23 pairs which can be the source of color vision deficiencies. Further studies of the human genome will show which chromosomes carry the encoding genes for rod monochromacy as this is still a subject under research and therefore this table will maybe undergo some adjustements in the near future.
Further readings:
Genetics Home Reference: Chromosomes
National Center for Biotechnology Information Map Viewer
Homozygosity mapping of achromatopsia to chromosome 2
A locus for autosomal achromatopsia on human chromosome 8
Related articles:
Tritanopia – Blue-Yellow Color Blindness
The Biology behind Red-Green Color Blindness
Daltonism – Named after John Dalton
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It seems perfectly reasonable that Rod Monochromacy could be caused by more than one “knockout mutation”, so maybe both 2 *and* 8 bear relevant genes, perhaps common to cone development in general.
What amazes me a bit, that the genes encoding S-cones are well determined and understood. In contrary rod monochromacy is not understood that well concerning genes which could be a cause. Of course it could be both chromosomes involved, maybe even more. It still needs more research to find out about it in detail.
is there a difference in the karyotype of a color blind individual and that of a normal individual??
As far as I understand it, there is no difference in the karyotype of a colorblind person and one with normal vision (aren’t colorblind people normal? :-)
The definition of karyotype is: A photographic representation of the chromosomes of a single cell, cut and arranged in pairs based on their banding pattern and size according to a standard classification.
Color blindness is just a slight mutation in some genes of some chromosomes. This mutations can’t be seen in a big scale picture of the whole chromosomes like the karyotype is.
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wow thx to that infomation i no ima get a A+ on ma project!!lol
This site was very useful for my report in the 8th grade. Thanks for all of the useful information that your website provided and answers that I neededf. Thanks alot. It was really really really really really really really really helpful.
thanks alot.
wow, you did an amazing job.
I am doing a research project in my school about colour blindness in the molecular genetics level, and this site helped me the most!
thank you so much for your information!!!
Awesome job on identifying the types of chromosomes involved in this disorder. Unlike a lot of other websites this was easy to understand and saved about half the work in my assignment.
Thank You.
I have three children with my (now ex) wife, two boys and a girl. My ex-wife is color blind and I have normal color vision. My daughter has normal color vision and my youngest son (14) is color blind.
My oldest son has normal color vision. From all that I have read, this is impossible. Any explanation?
Wayne, it is possible as it is always a bit more complicated then everybody learns at school.
If it is blue-yellow color blindness, this could be very well possible, as this is a autosomal dominant trait and 50% of the offspring will be affected.
But it could also be, that she is a compund mixed heterozygotes (carrying red and green color blindness in here) and showing a red-weakness. And one son inherited a very weak form you can’t measure very well.
Or mosaicism could be the cause. Whereas she is only a carrier, but shows such an atypical distribution of defective and good color receptors, that she tests positive on color blindness.
if the gene for colour blindness is carried in the X chromosome and females are XX chromosomes, why are they not affected?
One x chromosome comes from the mother, the second x from the father’s mother. For colour blindness (recessive) to be passed on both transmitted x chromosomes would have to carry the deficiency.
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Wayne, she cheated on you.
peole should know about tis disorder and dont juged the prolr who got i cause this is important…
is color blindness sex – linked?
and is this a result of translocation or deletion?
is color blindness sex-linked, chromosomal, or does it depend on the type of colorblindness a person may have?
this website really helped me for my 7th Grade genetic disorder project and every other website I went to were so confusing.