KIAA1704

KIAA1704 is found on the chromosome 13, at locus q14.12, with the genomic sequence starting at 45,563,687 bp and ending at 45,602,405 bp.[10]

KIAA1704 chromosomal location

KIAA1704GeneNeighborhood

KIAA1704 is located on the positive strand surrounded by 5 nearby genes.

Positive Orientation

• General Transcription Factor IIF (GTF2F2) is further downstream directed in the same orientation. Functionally, it binds to RNA Polymerase II.[11]

Negative Orientation

• Nuclear Fragile X Mental Retardation Protein Interacting Protein 1 (NUFIp1) shows RNA-binding activity with specific nuclear role for FMRP. This is an RNA-binding protein associated with Fragile X. Start sites are antisense to start of KIAA1704.[11]
• Potassium Channel Tetramerisation Domain Containing 4 (KCTD4) proposed to participate in potassium ion transport.[11]
• Tumor protein translationally controlled 1 (TPT1) is involved in calcium binding and microtubule stabilization.[11]
• Small nucleolar RNA, H/ACA box 31 (SNORA31) does not have a known function at this time.[11]

KIAA1704 has ubiquitous low to moderate expression patterns across body tissues (below 50%)[12]

NCBI GDS596 Microarray Expression Data

KIAA1704 Promoter Prediction

Using GenoMatix ElDorado analysis tools, the promoter was predicted to be 727 base pairs in length projecting into exon 1. There are two predicted transcriptional start sites for this promoter, shown on the adjacent image.[13]

KIAA1704 promoter showed significant histone 3 lysine 4 trimethylation peaks in K562 cells (erythroid cell line). It also showed increased relative expression in erythroid progenitors along with gene neighbors, NUFIP1 and TPT1.[14]

An additional study found that the proximal promoter is one of many thousand direct targets of transcription factor, Myc, in vivo.[15]

According to Ensembl, there are four coding splice variants. None of the alternative splice forms have experimental evidence associated. One splice variant undergoes non-sense mediated decay while another is predicted to splice the gene directly in half and retain amino acids 171–340.[16]

NCBI BLAST searches reveal that known mRNA orthologs exist in mammals, reptiles, birds, frogs, and fish with at least 65% sequence identity.[17]

Shown in the table below, KIAA1704 has significantly higher percentages of charged amino acids (D, K, KR, KRED) than the normal human protein and is mostly conserved within its orthologous proteins.[5]

KIAA1704 has protein orthologs extending through plants, shown in descending order of identity in the table below. Mammals have the highest level of conservation with 89 percent identity followed by birds, frogs, fish, invertebrates, insects, and plants.[17]

Concerning conserved domains, thus far, there does not appear to be much information about conserved motif, GPALPP(GF). This motif represents the neutral segments in this highly charged protein.

DUF3752 is generally found in Eukaryotes and is between 140 and 163 amino acids in length. It belongs to pfam12572, member of superfamily cl13947[18]

KIAA1704 Annotated Charge Multiple Sequence Alignment

Information provided by Statistical Analysis of Proteins (SAPS) tool.[5]

KIAA1704 is predicted by ExPASy tools to undergo several conserved post translational modifications including glycation, o-linked glycosylation, serine phosphorylation, threonine phosphorylation, and several kinase specific phosphorylation (PKC, PKA, and CKII).[6]

There are four conserved predicted alpha helices located towards the C terminus of the protein. The N terminus is predicted to be dominated by coiled regions.[19]

ExPASy PSORT predicts 74% chance of being localized to the nucleus.[6]