language-iconOld Web
English
Sign In

FAM83H

286077105732ENSG00000180921ENSG00000273889ENSMUSG00000046761Q6ZRV2Q148V8NM_198488NM_001168253NM_134087NP_940890NP_001161725NP_598848FAM83H is a gene in humans that encodes a protein known as FAM83H (uncharacterized protein FAM83H). FAM83H is targeted for the nucleus and it predicted to play a role in the structural development and calcification of tooth enamel. FAM83H is a gene in humans that encodes a protein known as FAM83H (uncharacterized protein FAM83H). FAM83H is targeted for the nucleus and it predicted to play a role in the structural development and calcification of tooth enamel. FAM83H is located on the long arm of chromosome 8 (8q24.3), starting at 143723933 and ending at 143738030. The FAM83H gene spans 14097 base pairs and is orientated on the—strand. The coding region is made up of 5,604 base pairs and 5 exons. FAM83H is ubiquitously expressed throughout the human body at relatively low levels. In humans, there is only one known major product of the FAM83H gene. There are no paralogs of FAM83H Below is a table of a variety of orthologs of the human FAM83H. The table include closely, intermediately and distantly related orthologs. Orthologs of the human protein FAM83H are listed above in descending order or date of divergence and then ascending order of percent identity. FAM83H is highly conserved throughout all orthologs, this is demonstrated with a 40% identity in the least similar ortholog. FAM83H has evolved slowly and evenly over time. The molecular weight of FAM83H is 127.1kD and contains 1179 amino acids. The isoelectric point is 6.52. There are no significant positive or negative charge clusters in the protein. There is a stretch of 21 0’s from 254-275 and a stretch of 24 0’s from 420-444.1 FAM83H is proline rich, being 10.32% protein, and is asparagine deficient with only 1.1%. The percent composition of each amino acid is fairly consistent throughout the orthologs of the protein. The most distant ortholog displays the most variance in amino acid composition.

[ "Exon", "Dominance (genetics)", "ENAM", "AMELX", "Phenotype", "Hypocalcified amelogenesis imperfecta", "FAM83H gene" ]
Parent Topic
Child Topic
    No Parent Topic
Baidu
map