{{Short description|Protein found in humans}} {{Infobox_gene}} '''Chromosome 9 open reading frame 50''' is a protein that in humans is encoded by the ''C9orf50'' gene.<ref>{{Cite web|url=https://www.ncbi.nlm.nih.gov/protein/NP_955382.3|title=uncharacterized protein C9orf50 [Homo sapiens] - Protein - NCBI|website=www.ncbi.nlm.nih.gov|access-date=2019-02-25}}</ref> C9orf50 has one other known alias, FLJ35803.<ref>{{Cite web|url=https://uswest.ensembl.org/Homo_sapiens/Gene/Summary?g=ENSG00000179058;r=9:129612225-129620776|title=Gene: C9orf50 (ENSG00000179058) - Summary - Homo sapiens - Ensembl genome browser 95|website=uswest.ensembl.org|access-date=2019-02-25}}{{Dead link|date=July 2025 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> In humans the gene coding sequence is 10,051 base pairs long, transcribing an mRNA of 1,624 bases that encodes a 431 amino acid protein.

== Gene ==

=== Location === In humans the gene is located on the negative strand at 9q34.11 and the coding sequence is 8,552 base pairs long.<ref name=":0">{{Cite web|url=https://www.genecards.org/cgi-bin/carddisp.pl?gene=C9orf50&keywords=c9orf50|title=C9orf50 Gene|last=|first=|date=|website=www.genecards.org|access-date=2019-02-25}}</ref> On human chromosome 9, the gene spans bases ''chr9:132,374,504-132,383,055''<ref name=":1">{{Cite web|url=https://www.ncbi.nlm.nih.gov/gene?cmd=retrieve&list_uids=375759|title=C9orf50 chromosome 9 open reading frame 50 [Homo sapiens (human)] - Gene - NCBI|website=www.ncbi.nlm.nih.gov|access-date=2019-02-25}}</ref> Near C9orf50 is ASB6 which is the gene directly before C9orf50 on the negative strand and on the positive strand is NTMT1 which is more than double the size of C9orf50.[[C9orf50# ftn1|[1]]][[C9orf50# ftn2|[2]]]

== Protein == thumb|C9orf50 Schematic Illustration using Dog2.0. The 431 amino acid is displayed showing regions of disorder in yellow, polyampholyte in red, and DUF4685 in teal. Other motifs are shown and labelled at the correct AA position. Pink circles represent sites of acetylation, teal represents glycation, and blue represents sumoylation. The C9orf50 protein has a molecular weight of 47,639 kD and consists 431 amino acids with a predicted isoelectric point of 10.38<ref name=":0" /> The C9orf50 protein contains the conserved domain in pfam15737- DUF4685, the function of which is not well understood and conserved in vertebrates. The protein is made up of 7 exons.

=== Isoforms === C9orf50 has 9 different splice isoforms (SI) and 11 different transcript variants (TV), the most common is isoform 1 and transcript variant 1.<ref name="ncbi.nlm.nih.gov">{{Cite web | url=https://www.ncbi.nlm.nih.gov/gene/375759 |title = C9orf50 chromosome 9 open reading frame 50 [Homo sapiens (human)] - Gene - NCBI}}</ref> thumb|C9orf50 Isoform table. Author Hannah Berhow thumb|C9orf50 Isoforms and Transcript Variants

== Domains == The protein can be analyzed as a whole as well as split into 3 parts including the N-terminal Domain of 193 residues, DUF4685 of 103 residues, and the C-terminal Domain of 135 residues. The full protein pI is similar to the average pI of the NTD, DUF4685, and CTD. Of these sections the NTD has the highest pI and mW but also has the most residues at 193 of 431.<ref>Gene https://www.ncbi.nlm.nih.gov/gene/375759</ref><ref>{{Cite web | url=https://web.expasy.org/compute_pi/ |title = ExPASy - Compute pI/Mw tool}}</ref> {| class="wikitable" |- ! C9orf50 !! pI !! mW kD !! Residues |- | Human Whole Protein || 10.38 || 47.6 || 431 |- | NTD || 11.14 || 21.1 || 193 |- | DUF4685 || 10.8 || 11.8 || 103 |- | CTD || 9.47 || 14.7 || 135 |}

== Composition == The compositional analysis of the C9orf50 protein reveals low amounts of I, M, Y and FIKMNY relative to humans and high amounts of R, and KR-ED. There are no findings for charge clusters, high scoring charged or uncharged segments, charge runs, patterns, high scoring hydrophobic or transmembrane segments. Three different unique spacings of C were found at positions 161, 190, and 342. C9orf50 is also found to have 3 repetitive structures, the first sequence PRLP_KLT occurs starting at position 30 and then is repeated at position 78. Another repetitive structure is SLLP at positions 99 and 398. The last repeat structure at 250 and 303 made of KAAL.<ref>{{Cite web | url=https://www.ebi.ac.uk/Tools/services/web/toolresult.ebi?jobId=saps-I20190404-150604-0222-8160736-p1m |title = EBI Tools: Job not available}}</ref>

== Tertiary Structure == Tertiary C9orf50 protein structures can be found using I-Tasser. This tool results in 5 visualized structures, the two with the highest C scores are -3.25 and -1.27.

== Gene level regulation ==

=== Promoter === The promoter region for C9orf50 was found using the Genomatix Gene2Promoter search engine.<ref name="Genomatix: Login Page">{{Cite web | url=https://www.genomatix.de/cgi-bin/welcome/welcome.pl?s=396f0114dfb6b4576e263b230dc6c906 | title=Genomatix: Login Page }}{{Dead link|date=July 2025 |bot=InternetArchiveBot |fix-attempted=yes }}</ref> This resulted in 6 found promoter regions. Only 2 of which were supported by transcripts and cage tags. The most supported promoter region spans 1,962 bases and is conserved in 6 of 8 orthologous loci with 945 cage tags. The transcription start site was determined to be located at 1,503 from a transcript with 7 exons supported by 118 cage tags.<ref name="Genomatix: Login Page"/>

=== Transcription factor binding sites === There are hundreds of transcription factors that are predicted to bind the promoter region. The promoter region transcription factors table highlight 20 of these.

== Transcript Level Regulation == C9orf50 5' UTR intermolecular base paired structure with the highest delta G is -323.4 kcal/mol. This is the lowest energy structure predicted for the 5'UTR region.<ref>{{Cite web | url=http://unafold.rna.albany.edu/?q=mfold |title = The Mfold Web Server {{pipe}} mfold.rit.albany.edu}}</ref> For the 3 ' UTR, the highest dG is -127.5 kcal/mol indicating that it is not as stable as the 5' UTR. thumb|C9orf50 3' UTR Stem Loop Structures thumb|C9orf50 5' UTR Stem Loop Structures

=== Tissue expression === RNA-seq data of C9orf50 has found a low expression level, 25-50th percentile, in most human tissues compared to all human proteins.<ref>{{Cite web | url=https://www.ncbi.nlm.nih.gov/geo/tools/profileGraph.cgi?ID=GDS3113:115495 |title = Gds3113 / 115495}}</ref> However, it is most highly expressed in testes, brain and gallbladder.<ref name="ncbi.nlm.nih.gov"/> C9orf50 protein expression is higher than the C9orf50 RNA expression.<ref>{{Cite web|url=https://www.sigmaaldrich.com/catalog/product/sigma/hpa026743?lang=en&region=US|title=Anti-C9orf50 antibody produced in rabbit Prestige Antibodies Powered by Atlas Antibodies, affinity isolated antibody, buffered aqueous glycerol solution {{pipe}} Sigma-Aldrich}}</ref> When studying in situ hybridization data, The mouse C9orf50 ortholog, symbol 1700001O22Rik, was used to compare protein expression against Beta-actin which is ubiquitously expressed and the analyses shows similar expression patterns in the mouse brain.<ref>{{Cite web | url=http://mouse.brain-map.org/gene/show/49439 | title=Gene Detail :: Allen Brain Atlas: Mouse Brain}}</ref> During development, the protein can be found in the fetal stages.<ref>{{Cite web | url=https://www.ncbi.nlm.nih.gov/UniGene/ESTProfileViewer.cgi?uglist=Hs.124223 |title = EST Profile - Hs.124223}}{{dead link|date=July 2025|bot=medic}}{{cbignore|bot=medic}}</ref>

=== Subcelluar expression === The protein has been located primarily in the nucleus and less so found in mitochondria and cytosol.<ref>{{Cite web | url=https://www.genscript.com/tools/wolf-psort | title=WoLF PSORT: Advanced Protein Subcellular Localization Prediction Tool - GenScript}}</ref> thumb|C9orf50 Promoter Region Transcription Factors

== Orthologs == There are no known paralogs of C9orf50. orthologs of C9orf50 have been found conserved across most subclasses of mammals with the furthest, opossum of the infraclass marsupialia, diverged 159 million years ago.<ref>{{Cite web|url=https://blast.ncbi.nlm.nih.gov/Blast.cgi?PAGE=Proteins&PROGRAM=blastp&BLAST_PROGRAMS=blastp&LINK_LOC=protein&PAGE_TYPE=BlastSearch&QUERY=|title=Protein BLAST: search protein databases using a protein query|website=blast.ncbi.nlm.nih.gov|access-date=2019-02-25}}</ref> This gene is not found in reptiles, amphibians, birds, or any other organisms evolved before mammals. A list of mammals in which C9orf50 is conserved is shown below. {| class="wikitable" |+C9orf50 Orthologs |Common Name |Taxonomic Group |Divergence from Humans (MYA) |NCBI Accession # |Protein Length (AA) |Sequence Identity to Humans% |- |Human |Hominini |0 |NP_955382.3 |431 |100 |- |Chimpanzee |Primates |6.65 |XP_016817319.1 |431 |97.22 |- |Gorilla |Primates |9.06 |XP_018889539.1 |435 |93.17 |- |Deer Mouse |Rodentia |90 |XP_006983488.1 |391 |46.14 |- |Prairie Vole |Rodentia |90 |XP_005346778.1 |370 |45.18 |- |American Pika |Lagomorpha |90 |XP_004593748.1 |579 |38.11 |- |Narrow Ridged Finless Porpoise |Cetacea |96 |XP_024617982.1 |473 |56.71 |- |Killer Whale |Cetacea |96 |XP_012388229.1 |343 |59.34 |- |Alpaca |Artiodactyla |96 |XP_006205645.1 |399 |53.83 |- |Black Flying Fox |Chiroptera |96 |XP_015449607.1 |432 |53.21 |- |Egyption Fruit bat |Chiroptera |96 |XP_015989428.1 |431 |53.01 |- |Goat |Artiodactyla |96 |XP_017910228.1 |438 |52.4 |- |Northern Fur Seal |Carnivora |96 |XP_025744313.1 |441 |52.36 |- |Grizzly Bear |Carnivora |96 |XP_026369526.1 |447 |50.63 |- |European Hedgehog |Soricomorpha |96 |XP_007527129.1 |419 |51.42 |- |Star Nosed Mole |Proboscidea |96 |XP_012576659.1 |383 |48.68 |- |Southern White Rhinoceros |Perissodactyla |96 |XP_014637447.1 |489 |47.25 |- |African Bush Elephant |Proboscidea |105 |XP_023401069.1 |527 |49.31 |- |Nine-Banded Armadillo |Cingulata |105 |XP_023443586.1 |476 |46.72 |- |Gray short tailed opossum |Didelpimorphia |159 |XP_007475193.1 |583 |32.56 |}

=== Evolution === C9orf50 is predicted to evolve more quickly than other common proteins including cytochrome C, hemoglobin beta, and fibrinogen alpha chain. thumb|C9orf50 Molecular Clock

=== Amino acid conservation === Important amino acids are characterized by those that were on the 100% consensus line created in MView of the strict ortholog multiple sequence alignment.<ref>{{Cite web | url=https://www.ebi.ac.uk/Tools/services/web/toolform.ebi?tool=MView&sequence=clustalo-I20190227-233229-0665-50488009-p1m | title=EBI Tools: Error}}</ref> Amino Acids in red represent conserved amino acids in DUF4685. 14 of the 22 highly conserved amino acids are found within this domain. Leucine occupies the most conserved positions of the C9orf50 protein. {| class="wikitable" |- ! Conserved Amino Acids !! C9orf50 AA Position |- | Proline || 33,325 |- | Leucine || 147, 155, 158, {{ font color | red |280, 285, }} 321, 328 |- | Phenylalanine || {{ font color | red |231, 275 }} |- | Arginine || {{ font color | red |272, 286 }} |- | Valine || {{ font color | red |273, }} 313 |- | Alanine || {{ font color | red |267 }} |- | Aspartic Acid || {{ font color | red |277 }} |- | Glutamic Acid || {{ font color | red |278, 289 }} |- | Threonine || {{ font color | red |279 }} |- | Tyrosine || {{ font color | red |287 }} |- | Tryptophan || {{ font color | red |288 }} |}

== Mutations == [[File:Conceptual Translation with Secondary Structure.pdf|thumb|Post Translational Modifications and Secondary Structure of C9orf50. PTMs for C9orf50 were found using the tools posted on the Expasy Protein Modifications site. The secondary structure for C9orf50 was predicted by using analysis from Gor, COILS, CFSSP, JPRED, and SOPMA.[[C9orf50# ftn1|<sup><sup>[1]</sup></sup>]]<sup>,[[C9orf50# ftn2|<sup>[2]</sup>]],[[C9orf50# ftn3|<sup>[3]</sup>]],[[C9orf50# ftn4|<sup>[4]</sup>]],[[C9orf50# ftn5|<sup>[5]</sup>]]</sup> Helix indicated by green cylinders, beta sheet indicated by blue arrows, and turn structures indicated by pink arrows were included below in the conceptual translation if they had a high prediction score. All the structures that were found in more than one analysis tool were also kept. The protein has no transmembrane sequences. ]] Common variants in C9orf50 were found with NCBI SNPGeneView.<ref>{{Cite web | url=https://www.ncbi.nlm.nih.gov/variation/view/?q=375759[geneid] |title = SNP linked to Gene (geneID:375759) Via Contig Annotation}}</ref>

{| class="wikitable" |- ! dbSNP rs# Cluster ID !! Function !! dbSNP Allele !! Amino Acid Position |- | rs146521610 || Synonymous || V → G || 317 |- | rs566893379 || Synonymous || S → T || 310 |- | rs111868243 || Synonymous || S → A || 258 |- | rs918165 || Missense || K → A || 248 |- | rs141573674 || Missense || S → A || 201 |- | rs759058008 || Frameshift || Deleted L || 189 |- | rs111606531 || Synonymous || A → T || 86 |- | rs146618124 || Missense || S → C || 52 |- | rs372378735 || Synonymous || G → A || 45 |- | rs751493011 || Nonsense || Insert T || 11 |}

==References== {{Reflist}}