What gene deficiency is the cause of manletisam

[iam good boy]

Fuarrk

 

[Deleted member 30942]

Short parents

 

[iam good boy]

Short parents

Like what type of genetic material do they lack

 

[chadmanlet04]

Like what type of genetic material do they lack

height

 

[iam good boy]

height

Nigger what is the name of that genetic materal code for example autisam is caused by AVPR1a, DISC1, DYX1C1, ITGB3, SLC6A4, RELN, RPL10 and SHANK3.

 

[chadmanlet04]

Nigger what is the name of that genetic materal code for example autisam is caused by AVPR1a, DISC1, DYX1C1, ITGB3, SLC6A4, RELN, RPL10 and SHANK3.

FGFR3: This is a rare genetic mutation involved in bone and brain tissue development. Specific mutations in this gene cause almost all cases of achondroplasia, a form of short-limbed dwarfism. The mutations cause this gene to be overly active and interfere with skeletal development.

FBN1: This gene codes for the protein that allows microfibrils to form. These molecules form elastic fibers, which enable the skin, ligaments, and blood vessels to stretch. They also support other structures like bones, nerves, and muscles.

GH1: This gene encodes for a growth hormone protein. Gene mutations can cause isolated growth hormone deficiency, which causes slow growth and short stature.

EVC: The function of the protein that this gene codes for is unknown. However, experts believe it is involved in normal growth and development. Mutations in this gene cause Ellis-van Creveld syndrome, characterized by dwarfism, abnormal nails and teeth, and heart defects.

GPC3: This gene encodes for a protein involved with cell growth and division. In most cases, it appears to restrict growth although it may have the opposite effect in some parts of the body. Several mutations in this gene may cause Simpson-Golabi-Behmel syndrome, a condition characterized by infants larger than normal at birth that continue to grow and gain weight at an accelerated rate.