Fam221b

FAM221B can be found around the end of the short arm of human chromosome 9.

General position of FAM221B on Human Chromosome 9 (marked by red line)

Gene neighborhood of FAM221B

FAM221B is expressed at low levels in human and mouse tissues. Expression is highest in germ cell tissues and cells. This differential expression is most pronounced in testes tissue. Compared to Homo sapiens, Mus musculus shows more differential expression of FAM221B in testes tissue [4] [5] [6] [7] . Mature beta cells express FAM221B at higher rates than do fetal beta cells [8] .

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  FAM221B expression for BioGPS dataset in various tissues in Homo sapiens
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  FAM221B expression for GEO dataset GDS 3113 in various tissues in Homo sapiens
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  FAM221B expression for BioGPS dataset in various tissues in Mus musculus
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  FAM221B expression for GEO dataset GDS 3142 in various tissues in Mus musculus

FAM221B has a total of 5 transcript variants: the putative sequence, Isoform X1 [9] , Isoform X2 [10] , Isoform X3 [11] , and Isoform X4. Isoform X4 does not exist in humans but is found in various primates.

Various FAM221B spliced isoforms and their exons as shown in AceView

There are a total of six exons in the putative sequence of FAM221B. However, a total of seven exons exist for FAM221B, as the seventh exon is an alternative exon.

The putative sequence for FAM221B is 402 amino acids long and weighs 45.4 kilodaltons. Amino acids expressed at abnormal rates include Histidine, Cysteine, Glutamic acid, and Tyrosine. When compared to typical proteins, FAM221B expresses Histidine at a much higher frequency at 6.0% of protein, Cysteine at a slightly higher frequency at 4.7% of protein, Glutamic acid at a slightly higher frequency at 11.4% of protein, and Tyrosine at a slightly lower frequency at 1.0% of protein [15] . The isoelectric point of FAM221B is 5.264, suggesting FAM221B is an acidic protein at a normal physiological pH (7.4) [15] . There is strong evidence that FAM221B is a protein found within the nucleus [16] .

FAM221B is predicted to have two distinct alpha helices in its secondary structure [17] [18] [19] . Secondary structure predicting programs predict beta sheets but are not as consistent as the two alpha helices.

FAM221B is predicted to have a high number of phosphorylation sites.

There is evidence that FAM221B interacts with the proteins Autophagy related 13 (KIAA0652), RB1-inducible coiled-coil 1 (RB1CC1), and Ephrin-B3 (EFNB3) [20] . These proteins are predicted to be localized in the nucleus at the same confidence level as FAM221B.

One paralog exists for FAM221B in humans: FAM221A [21] . FAM221A and FAM221B's ancestral gene is predicted to have diverged in prokarya.

There are three conserved domains within FAM221B: DUF4475 super family [22] , PRCC super family [23] , and Caprin-1_C [24] . DUF4475 is the most conserved domain of the three.