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SIX1
HPA
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  • SIX1
PROTEIN SUMMARY GENE INFORMATION RNA DATA ANTIBODY DATA
GENERAL INFORMATIONi

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.

SIX1
Synonyms DFNA23
Gene descriptioni

Full gene name according to HGNC.

SIX homeobox 1
Protein classi

Assigned HPA protein class(es) for the encoded protein(s).

Cancer-related genes
Disease related genes
Human disease related genes
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.

Intracellular
Protein evidence Evidence at protein level (all genes)
GENE INFORMATIONi

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 14
Cytoband q23.1
Chromosome location (bp) 60643421 - 60658259
Number of transcriptsi

Number of protein-coding transcripts from the gene as defined by Ensembl.

2
Ensembl ENSG00000126778 (version 109)
Entrez gene 6495
HGNC HGNC:10887
UniProt Q15475 (UniProt - Evidence at protein level)
neXtProt NX_Q15475
GeneCards SIX1
Antibodypedia SIX1 antibodies


PROTEIN FUNCTION
Protein function (UniProt)i

Useful information about the protein provided by UniProt.

Transcription factor that is involved in the regulation of cell proliferation, apoptosis and embryonic development (By similarity). Plays an important role in the development of several organs, including kidney, muscle and inner ear (By similarity). Depending on context, functions as a transcriptional repressor or activator (By similarity). Lacks an activation domain, and requires interaction with EYA family members for transcription activation 1. Mediates nuclear translocation of EYA1 and EYA2 2. Binds the 5'-TCA[AG][AG]TTNC-3' motif present in the MEF3 element in the MYOG promoter and CIDEA enhancer 3, 4, 5, 6. Regulates the expression of numerous genes, including MYC, CCND1 and EZR (By similarity). Acts as an activator of the IGFBP5 promoter, probably coactivated by EYA2 (By similarity). Repression of precursor cell proliferation in myoblasts is switched to activation through recruitment of EYA3 to the SIX1-DACH1 complex (By similarity). During myogenesis, seems to act together with EYA2 and DACH2 (By similarity). Regulates the expression of CCNA1 7. Promotes brown adipocyte differentiation (By similarity).... show less
Molecular function (UniProt)i

Keywords assigned by UniProt to proteins due to their particular molecular function.

Activator, Developmental protein, DNA-binding, Repressor
Biological process (UniProt)i

Keywords assigned by UniProt to proteins because they are involved in a particular biological process.

Apoptosis, Transcription, Transcription regulation
Gene summary (Entrez)i

Useful information about the gene from Entrez

The protein encoded by this gene is a homeobox protein that is similar to the Drosophila 'sine oculis' gene product. This gene is found in a cluster of related genes on chromosome 14 and is thought to be involved in limb development. Defects in this gene are a cause of autosomal dominant deafness type 23 (DFNA23) and branchiootic syndrome type 3 (BOS3). [provided by RefSeq, Jul 2008]... show less
PROTEIN INFORMATIONi

The protein information section displays alternative protein-coding transcripts (splice variants) encoded by this gene according to the Ensembl database.

The Splice variant identifier links to the Ensembl website protein summary for the selected splice variant. The data in the Swissprot and TrEMBL columns links to corresponding pages in the UniProt database.

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 length of the protein (amino acid residues according to Ensembl), molecular mass (kDalton), predicted signal peptide and number of predicted transmembrane region(s) according to in-house majority decision methods based on sets of predictors are also reported.
Splice variant SwissProt TrEMBL Protein class Gene ontology Length & mass Signal peptide
(predicted)
Transmembrane regions
(predicted)
SIX1-202
ENSP00000452700
ENST00000554986
H0YK85
[Direct mapping] Homeobox protein SIX1
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Cancer-related genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Missense Mutations
Human disease related genes
   Congenital malformations
   Other congenital malformations
   Nervous system diseases
   Ear disease
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000976 [transcription cis-regulatory region binding]
GO:0003700 [DNA-binding transcription factor activity]
GO:0045892 [negative regulation of DNA-templated transcription]
Show all
111 aa
12 kDa
No 0
SIX1-205
ENSP00000494686
ENST00000645694
Q15475
[Direct mapping] Homeobox protein SIX1
Show all
Predicted intracellular proteins
   Intracellular proteins predicted by MDM and MDSEC
Transcription factors
   Helix-turn-helix domains
Cancer-related genes
   COSMIC somatic mutations in cancer genes
   COSMIC Somatic Mutations
   COSMIC Missense Mutations
Disease related genes
Human disease related genes
   Congenital malformations
   Other congenital malformations
   Nervous system diseases
   Ear disease
Mapped to neXtProt
   neXtProt - Evidence at protein level
Protein evidence (Ezkurdia et al 2014)
Show all
GO:0000122 [negative regulation of transcription by RNA polymerase II]
GO:0000785 [chromatin]
GO:0000976 [transcription cis-regulatory region binding]
GO:0000978 [RNA polymerase II cis-regulatory region sequence-specific DNA binding]
GO:0000981 [DNA-binding transcription factor activity, RNA polymerase II-specific]
GO:0001223 [transcription coactivator binding]
GO:0001228 [DNA-binding transcription activator activity, RNA polymerase II-specific]
GO:0001657 [ureteric bud development]
GO:0001658 [branching involved in ureteric bud morphogenesis]
GO:0001759 [organ induction]
GO:0001822 [kidney development]
GO:0003151 [outflow tract morphogenesis]
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:0005730 [nucleolus]
GO:0005737 [cytoplasm]
GO:0006355 [regulation of DNA-templated transcription]
GO:0006357 [regulation of transcription by RNA polymerase II]
GO:0006915 [apoptotic process]
GO:0007219 [Notch signaling pathway]
GO:0007382 [specification of segmental identity, maxillary segment]
GO:0007389 [pattern specification process]
GO:0007519 [skeletal muscle tissue development]
GO:0007605 [sensory perception of sound]
GO:0008582 [regulation of synaptic assembly at neuromuscular junction]
GO:0010467 [gene expression]
GO:0010468 [regulation of gene expression]
GO:0014033 [neural crest cell differentiation]
GO:0014842 [regulation of skeletal muscle satellite cell proliferation]
GO:0014857 [regulation of skeletal muscle cell proliferation]
GO:0021610 [facial nerve morphogenesis]
GO:0022008 [neurogenesis]
GO:0030855 [epithelial cell differentiation]
GO:0030878 [thyroid gland development]
GO:0030910 [olfactory placode formation]
GO:0032880 [regulation of protein localization]
GO:0034504 [protein localization to nucleus]
GO:0035909 [aorta morphogenesis]
GO:0042472 [inner ear morphogenesis]
GO:0042474 [middle ear morphogenesis]
GO:0043066 [negative regulation of apoptotic process]
GO:0043524 [negative regulation of neuron apoptotic process]
GO:0043565 [sequence-specific DNA binding]
GO:0043586 [tongue development]
GO:0045664 [regulation of neuron differentiation]
GO:0045892 [negative regulation of DNA-templated transcription]
GO:0045893 [positive regulation of DNA-templated transcription]
GO:0045944 [positive regulation of transcription by RNA polymerase II]
GO:0048538 [thymus development]
GO:0048665 [neuron fate specification]
GO:0048699 [generation of neurons]
GO:0048701 [embryonic cranial skeleton morphogenesis]
GO:0048704 [embryonic skeletal system morphogenesis]
GO:0048705 [skeletal system morphogenesis]
GO:0048741 [skeletal muscle fiber development]
GO:0048839 [inner ear development]
GO:0048856 [anatomical structure development]
GO:0050678 [regulation of epithelial cell proliferation]
GO:0051450 [myoblast proliferation]
GO:0051451 [myoblast migration]
GO:0060037 [pharyngeal system development]
GO:0061055 [myotome development]
GO:0061197 [fungiform papilla morphogenesis]
GO:0061551 [trigeminal ganglion development]
GO:0071599 [otic vesicle development]
GO:0072075 [metanephric mesenchyme development]
GO:0072095 [regulation of branch elongation involved in ureteric bud branching]
GO:0072107 [positive regulation of ureteric bud formation]
GO:0072172 [mesonephric tubule formation]
GO:0072193 [ureter smooth muscle cell differentiation]
GO:0072198 [mesenchymal cell proliferation involved in ureter development]
GO:0072513 [positive regulation of secondary heart field cardioblast proliferation]
GO:0086100 [endothelin receptor signaling pathway]
GO:0090103 [cochlea morphogenesis]
GO:0090190 [positive regulation of branching involved in ureteric bud morphogenesis]
GO:0090336 [positive regulation of brown fat cell differentiation]
GO:1905243 [cellular response to 3,3',5-triiodo-L-thyronine]
GO:1990837 [sequence-specific double-stranded DNA binding]
GO:2000288 [positive regulation of myoblast proliferation]
GO:2000729 [positive regulation of mesenchymal cell proliferation involved in ureter development]
GO:2001014 [regulation of skeletal muscle cell differentiation]
Show all
284 aa
32.2 kDa
No 0

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