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General description of the gene and the encoded protein(s) using information from HGNC and Ensembl, as well as predictions made by the Human Protein Atlas project.
Gene namei
Official gene symbol, which is typically a short form of the gene name, according to HGNC.
Disease related genes Human disease related genes Plasma proteins Transcription factors
Predicted locationi
All transcripts of all genes have been analyzed regarding the location(s) of corresponding protein based on prediction methods for signal peptides and transmembrane regions.
Genes with at least one transcript predicted to encode a secreted protein, according to prediction methods or to UniProt location data, have been further annotated and classified with the aim to determine if the corresponding protein(s) are secreted or actually retained in intracellular locations or membrane-attached.
Remaining genes, with no transcript predicted to encode a secreted protein, will be assigned the prediction-based location(s).
The annotated location overrules the predicted location, so that a gene encoding a predicted secreted protein that has been annotated as intracellular will have intracellular as the final location.
Gene information from Ensembl and Entrez, as well as links to available gene identifiers are displayed here. Information was retrieved from Ensembl if not indicated otherwise.
Chromosome
15
Cytoband
q22.31
Chromosome location (bp)
66702236 - 66782849
Number of transcriptsi
Number of protein-coding transcripts from the gene as defined by Ensembl.
The Structure section provides predicted structures from the Alphafold protein structure database and available experimental structures from Protein Data Bank (PDB).
In the Structure drop-down menu all experimental structures from PDB are available for selection and display. The structures are displayed using the NGL Viewer and can be zoomed-in and rotated either manually or by checking the Autorotate box. The Color scheme can be selected to show the residue index, chain name or confidence score (as B-factors and pLDDT score for experimental and predicted structures, respectively). The positions for available antigen sequences in the structure are shown if Antigens is turned to ON, and the Variants slider can be used to show the positions of clinical and population variants.https://github.com/nglviewer/ngl
The protein browser displays the antigen location on the target protein(s) and the features of the target protein. The tabs at the top of the protein view section can be used to switch between the different splice variants to which an antigen has been mapped.
At the top of the view, the position of the antigen (identified by the corresponding HPA identifier) is shown as a green bar. A yellow triangle on the bar indicates a <100% sequence identity to the protein target.
Below the antigens, the maximum percent sequence identity of the protein to all other proteins from other human genes is displayed, using a sliding window of 10 aa residues (HsID 10) or 50 aa residues (HsID 50). The region with the lowest possible identity is always selected for antigen design, with a maximum identity of 60% allowed for designing a single-target antigen (read more).
The curve in blue displays the predicted antigenicity i.e. the tendency for different regions of the protein to generate an immune response, with peak regions being predicted to be more antigenic.The curve shows average values based on a sliding window approach using an in-house propensity scale. (read more).
If a signal peptide is predicted by a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius (turquoise) and/or transmembrane regions (orange) are predicted by MDM, these are displayed.
Low complexity regions are shown in yellow and InterPro regions in green. Common (purple) and unique (grey) regions between different splice variants of the gene are also displayed (read more), and at the bottom of the protein view is the protein scale.
SMAD6-201
SMAD6-203
PROTEIN INFORMATIONi
The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.
The ENSP identifier links to the Ensembl website protein summary, while the ENST identifier links to the Ensembl website transcript summary for the selected splice variant. The data in the UniProt column can be expanded to show links to all matching UniProt identifiers for this protein.
The protein classes assigned to this protein are shown if expanding the data in the protein class column. Parent protein classes are in bold font and subclasses are listed under the parent class.
The Gene Ontology terms assigned to this protein are listed if expanding the Gene ontology column. The length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide (according to a majority of the signal peptide predictors SPOCTOPUS, SignalP 4.0, and Phobius) and the number of predicted transmembrane region(s) (according to MDM) are also reported.
O43541 [Direct mapping] Mothers against decapentaplegic homolog 6
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Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Plasma proteins Transcription factors beta-Hairpin exposed by an alpha/beta-scaffold Disease related genes Human disease related genes Congenital malformations Congenital malformations of the circulatory system Mapped to neXtProt neXtProt - Evidence at protein level
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GO:0000785 [chromatin] GO:0000976 [transcription regulatory region sequence-specific DNA binding] GO:0001657 [ureteric bud development] GO:0003148 [outflow tract septum morphogenesis] GO:0003170 [heart valve development] GO:0003180 [aortic valve morphogenesis] GO:0003183 [mitral valve morphogenesis] GO:0003184 [pulmonary valve morphogenesis] GO:0003281 [ventricular septum development] GO:0003677 [DNA binding] GO:0003682 [chromatin binding] GO:0003700 [DNA-binding transcription factor activity] GO:0005515 [protein binding] GO:0005634 [nucleus] GO:0005654 [nucleoplasm] GO:0005667 [transcription regulator complex] GO:0005737 [cytoplasm] GO:0005794 [Golgi apparatus] GO:0005829 [cytosol] GO:0006355 [regulation of transcription, DNA-templated] GO:0006955 [immune response] GO:0007179 [transforming growth factor beta receptor signaling pathway] GO:0007352 [zygotic specification of dorsal/ventral axis] GO:0008285 [negative regulation of cell population proliferation] GO:0009653 [anatomical structure morphogenesis] GO:0010991 [negative regulation of SMAD protein complex assembly] GO:0016604 [nuclear body] GO:0030154 [cell differentiation] GO:0030279 [negative regulation of ossification] GO:0030509 [BMP signaling pathway] GO:0030512 [negative regulation of transforming growth factor beta receptor signaling pathway] GO:0030514 [negative regulation of BMP signaling pathway] GO:0031589 [cell-substrate adhesion] GO:0031625 [ubiquitin protein ligase binding] GO:0032496 [response to lipopolysaccharide] GO:0032991 [protein-containing complex] GO:0034616 [response to laminar fluid shear stress] GO:0034713 [type I transforming growth factor beta receptor binding] GO:0035904 [aorta development] GO:0042802 [identical protein binding] GO:0043066 [negative regulation of apoptotic process] GO:0043627 [response to estrogen] GO:0045444 [fat cell differentiation] GO:0045668 [negative regulation of osteoblast differentiation] GO:0046872 [metal ion binding] GO:0060394 [negative regulation of pathway-restricted SMAD protein phosphorylation] GO:0060395 [SMAD protein signal transduction] GO:0060976 [coronary vasculature development] GO:0070410 [co-SMAD binding] GO:0070411 [I-SMAD binding] GO:0070412 [R-SMAD binding] GO:0070698 [type I activin receptor binding] GO:0071144 [heteromeric SMAD protein complex] GO:0140416 [DNA-binding transcription factor inhibitor activity] GO:1902895 [positive regulation of pri-miRNA transcription by RNA polymerase II]
H0YK80 [Direct mapping] Mothers against decapentaplegic homolog 6
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Predicted intracellular proteins Intracellular proteins predicted by MDM and MDSEC Human disease related genes Congenital malformations Congenital malformations of the circulatory system
The Human Protein Atlas project is funded
