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| Aliases | TMCO6 , PRO1580, transmembrane and coiled-coil domains 6 | ||||||||||||||||||||||||||||||||||||||||||||||||||
| External IDs | MGI: 1919233 HomoloGene: 12431 GeneCards: TMCO6 | ||||||||||||||||||||||||||||||||||||||||||||||||||
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Transmembrane and coiled-coil domain 6, TMCO6, is a protein that in humans is encoded by the TMCO6 gene with aliases of PRO1580, HQ1580 or FLJ39769.1. [5]
The human TMCO6 is found on chromosome 5 (position 5q31.3). [6] The entire gene spans 5568 base pairs on the positive strand of chromosome 5 (140019113-140024689bp) but is alternately spliced into different variants. There are three known variants for TMCO6. Variant 1 is the longest and variant 2 and 3 are spliced into shorter mRNA strands. [7] There is also a predicted variants X1-X7.
TMCO6 is expressed in liver tissue and is found during the fetal stage of development in humans. [7] [8]
Orthologs of the TMCO6 protein have been found among sequenced organisms with the exception of invertebrates, fungi, plants and bacteria. [5] Tmco6 (transmembrane and coiled-coil domains 6) - Rat Genome Database. [9] This includes close primates to some distant fish. Graphs show the evolutionary rate of TMCO6 with respect to different species and compared to other proteins. It is concluded that TMCO6 is a fairly fast evolving protein, similar to fibrinogen.
There are four known isoforms associated with this gene/protein (1, 2, 3 and X2). [7] The longest variant of TMCO6 is variant 1, encoded by a 12-exon long, 1,925 base pair mRNA sequence. Variant 2 is the second longest at 1,907 base pairs in length and also consists of 12 exons. This transcript variant has an alternate splice site in the central coding region that does not alter the reading frame. Variant 3 has a total length of 1,614 base pairs and differs from variant 1 because it lacks two consecutive exons. It has an alternative splice site in the 5’ region that causes the translation to initiate downstream at an in frame AUG. Variant X2 is predicted using computational analysis and is 1,892 base pairs in length. [7]
The TMCO6 protein is found in the membrane and is considered a multi-pass membrane protein. [5] There is evidence of its presence in the nucleus, cytosol, ER, mitochondria and the plasma membrane. [5] The predicted molecular weight of Isoform 1 in humans, but is conserved, is 55kDa. [6] Variant 1 is translated into a 499 amino acid sequence isoform. [6] [7] Isoform 2, encoded by transcript variant 2, is 493 amino acids in length and has a predicted molecular weight of 54 kDa. Transcript variant 3 encodes isoform 3 which is the shortest protein because of its spliced N-terminus. Isoform 3 is 253 amino acids in length with a molecular weight of 28kDa.
Evidence of two reserved ARM superfamily domains are shown in the TMCO6 protein. [6] The ARM domain, Armadillo/ beta-catenin-like-repeat, is about a 40 amino acid long tandem repeat that forms superhelix of helices. Another feature is that TMCO6 has an Arginine rich region that is within the coil-coiled region. [10] This indicates that the Arg rich area might be an important structural feature of the coiled-coil region. There are 17 regions for protein binding, 2 transmembrane domains and an addition of a poly-A tail to the mRNA. [10] An SRP1 is also found from the 23-399 amino acids. The SRP1 domain is Karyopherin(importin) alpha. [10] This is involved in the exchange of molecules from the nucleus and the cytoplasm. The exchange involves the active transport by a carrier protein called karyopherins. [10] A di-leucine motif is also abundant in TMCO6. This motif is commonly known to be a lysosome targeting motif. [11] A nuclear localization sequence of 5 positive amino acids is found near the 5' end indicating its transport to the nucleus.
The 5' and 3' end of TMCO6 is predicted to be located on the cytoplasmic side of the membrane. There is a small portion located in the non-cytoplasmic side.
Function of the conserved ARM domain and SRP1 domains are known. [6] The ARM domains play a role in mediating the interaction of beta-catenin with its ligand. They are responsible for transduction of the Wnt signal, intracellular signaling and cytoskeletal regulation. The SRP1 domain encodes alpha-Karyopherin (importin) and is known for intracellular trafficking and secretion on the membrane. TMCO6 is thought to be involved in the transport of molecules through the nuclear membrane.
Two-hybrid experimental evidence suggests UBQLN1, or ubiquilin 1, has a high potential to interact with TMCO6. [5] [12]
Transmembrane protein 8B is a protein that in humans is encoded by the TMEM8B gene. It encodes for a transmembrane protein that is 338 amino acids long, and is located on human chromosome 9. Aliases associated with this gene include C9orf127, NAG-5, and NGX61.
Coiled-coil domain containing 109B (CCDC109B) is a potential calcium uniporter protein found in the membrane of human cells and is encoded by the CCDC109B gene. While CCDC109B is a transmembrane protein it is unclear if it is located within the cell membrane or mitochondrial membrane.
Coiled-coil domain-containing protein 138, also known as CCDC138, is a human protein encoded by the CCDC138 gene. The exact function of CCDC138 is unknown.
Megf8 also known as Multiple Epidermal Growth Factor-like Domains 8, is a protein coding gene that encodes a single pass membrane protein, known to participate in developmental regulation and cellular communication. It is located on chromosome 19 at the 49th open reading frame in humans (19q13.2). There are two isoform constructs known for MEGF8, which differ by a 67 amino acid indel. The isoform 2 splice version is 2785 amino acids long, and predicted to be 296.6 kdal in mass. Isoform 1 is composed of 2845 amino acids and predicted to weigh 303.1 kdal. Using BLAST searches, orthologs were found primarily in mammals, but MEGF8 is also conserved in invertebrates and fishes, and rarely in birds, reptiles, and amphibians. A notably important paralog to multiple epidermal growth factor-like domains 8 is ATRNL1, which is also a single pass transmembrane protein, with several of the same key features and motifs as MEGF8, as indicated by Simple Modular Architecture Research Tool (SMART) which is hosted by the European Molecular Biology Laboratory located in Heidelberg, Germany. MEGF8 has been predicted to be a key player in several developmental processes, such as left-right patterning and limb formation. Currently, researchers have found MEGF8 SNP mutations to be the cause of Carpenter syndrome subtype 2.
Coiled-coil domain 47 (CCDC47) is a gene located on human chromosome 17, specifically locus 17q23.3 which encodes for the protein CCDC47. The gene has several aliases including GK001 and MSTP041. The protein itself contains coiled-coil domains, the SEEEED superfamily, a domain of unknown function (DUF1682) and a transmembrane domain. The function of the protein is unknown, but it has been proposed that CCDC47 is involved in calcium ion homeostasis and the endoplasmic reticulum overload response.
TMEM143 is a protein that in humans is encoded by TMEM143 gene. TMEM143, a dual-pass protein, is predicted to reside in the mitochondria and high expression has been found in both human skeletal muscle and the heart. Interaction with other proteins indicate that TMEM143 could potentially play a role in tumor suppression/expression and cancer regulation.
GPATCH11 is a protein that in humans is encoded by the G-patch domain containing protein 11 gene. The gene has four transcript variants encoding two functional protein isoforms and is expressed in most human tissues. The protein has been found to interact with several other proteins, including two from a splicing pathway. In addition, GPATCH11 has orthologs in all taxa of the eukarya domain.
Uncharacterized protein C12orf60 is a protein that in humans is encoded by the C12orf60 gene. The gene is also known as LOC144608 or MGC47869. The protein lacks transmembrane domains and helices, but it is rich in alpha-helices. It is predicted to localize in the nucleus.
Transmembrane and coiled-coil domains 4, TMCO4, is a protein in humans that is encoded by the TMCO4 gene. Currently, its function is not well defined. It is transmembrane protein that is predicted to cross the endoplasmic reticulum membrane three times. TMCO4 interacts with other proteins known to play a role in cancer development, hinting at a possible role in the disease of cancer.
GRAM domain containing 1B, also known as GRAMD1B, Aster-B and KIAA1201, is a cholesterol transport protein that is encoded by the GRAMD1B gene. It contains a transmembrane region and two domains of known function; the GRAM domain and a VASt domain. It is anchored to the endoplasmic reticulum. This highly conserved gene is found in a variety of vertebrates and invertebrates. Homologs are found in yeast.
Chromosome 8 open reading frame 58 is an uncharacterised protein that in humans is encoded by the C8orf58 gene. The protein is predicted to be localized in the nucleus.
TMEM44 is a protein that in humans is encoded by the TMEM44 gene. DKFZp686O18124 is a synonym of TMEM44.
Uncharacterized protein C17orf78 is a protein encoded by the C17orf78 gene in humans. The name denotes the location of the parent gene, being at the 78th open reading frame, on the 17th human chromosome. The protein is highly expressed in the small intestine, especially the duodenum. The function of C17orf78 is not well defined.
Leucine rich single-pass membrane protein 2 is a single-pass membrane protein rich in leucine, that in humans is encoded by the LSMEM2 gene. The LSMEM2 protein is conserved in mammals, birds, and reptiles. In humans, LSMEM2 is found to be highly expressed in the heart, skeletal muscle and tongue.
Coiled-coil domain containing 121 (CCDC121) is a protein encoded by the CCDC121 gene in humans. CCDC121 is located on the minus strand of chromosome 2 and encodes three protein isoforms. All isoforms of CCDC121 contain a domain of unknown function referred to as DUF4515 or pfam14988.
Transmembrane emp24 domain-containing protein 5 is a protein that in humans is encoded by the TMED5 gene.
Transmembrane protein 101 (TMEM101) is a protein that in humans is encoded by the TMEM101 gene. The TMEM101 protein has been demonstrated to activate the NF-κB signaling pathway. High levels of expression of TMEM101 have been linked to breast cancer.
Solute carrier family 66 member 3 is a gene in humans that encodes the protein SLC66A3. The function of the SLC66A3 protein is not yet well understood but belongs to a family of five evolutionarily related proteins, the SLC66 lysosomal amino acid transporters. SLC66A3 is localized to the endoplasmic reticulum and has four transmembrane domains.
KIAA1143 is an uncharacterized protein in humans that is encoded by the KIAA1143 gene. it may play a role in cell growth mechanisms and regulation/creation of cytoskeletal structure. This gene is located on chromosome 3 on the minus strand
Chromosome 13 Open Reading Frame 46 is a protein which in humans is encoded by the C13orf46 gene. In humans, C13orf46 is ubiquitously expressed at low levels in tissues, including the lungs, stomach, prostate, spleen, and thymus. This gene encodes eight alternatively spliced mRNA transcript, which produce five different protein isoforms.
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